UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 6-K

Report of Foreign Private Issuer

Pursuant to Rule 13a-16 or 15d-16 of

the Securities Exchange Act of 1934

May 8, 2025

 

Commission File Number: 001-36622

PROQR THERAPEUTICS N.V.

Zernikedreef 9

2333 CK Leiden

The Netherlands

Tel: +31 88 166 7000

(Address, Including ZIP Code, and Telephone Number,

Including Area Code, of Registrant’s Principal Executive Offices)

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.

Form 20-F    Form 40-F 

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1): 

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(7): 


Furnished as Exhibit 99.1 to this Report on Form 6-K are the unaudited financial statements of ProQR Therapeutics N.V. (the “Company”) for the three-month period ended March 31, 2025, and furnished as Exhibit 99.2 to this Report on Form 6-K is a press release of ProQR Therapeutics N.V. dated May 8, 2025, announcing the Company’s results for the three-month period ended March 31, 2025. 

On May 8, 2025, the Company issued a press release titled, “ProQR Announces First Quarter 2025 Operating and Financial Results,” announcing the Company’s results for the three-month period ended March 31, 2025 and providing a business update. A copy of this press release is attached hereto as Exhibit 99.2 and is incorporated herein by reference.

ProQR hereby incorporates by reference the information contained herein into ProQR’s registration statements on Form F-3 (File No. 333-282419, File No. 333-270943, File No. 333-263166 and File No. 333-285767).



SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

PROQR THERAPEUTICS N.V.

Date: May 8, 2025

By:

/s/ Jurriaan Dekkers

Jurriaan Dekkers

Chief Financial Officer


0001612940--12-312025Q1falseProQR Therapeutics N.V.6-K2025-03-31P10YP10YP11YP5YP30D0001612940prqr:PontifaxAndKreosWarrantsMember2022-09-012022-09-300001612940prqr:SharePurchaseAgreementWithEliLillyAndCompanyMember2024-10-250001612940prqr:UnderwritersOptionInConnectionToOctober2024UnderwrittenPublicOfferingMember2024-10-310001612940prqr:EliLillyAndCompanyMember2025-01-012025-03-310001612940prqr:ShelfRegistrationStatement2024Member2024-09-300001612940prqr:AtMarketOfferingsWithCantorFitzgeraldAndCoUnderShelfRegistrationStatementMember2024-09-300001612940prqr:RettSyndromeResearchTrustMember2024-01-310001612940prqr:OfficeAndLaboratoryFacilitiesAtZernikedreefInLeidenNetherlandsMember2020-07-012020-07-010001612940prqr:OfficeAndLaboratoryFacilitiesAtZernikedreefInLeidenNetherlandsMember2020-12-012020-12-310001612940prqr:OfficeAndLaboratoryFacilitiesAtZernikedreefInLeidenNetherlandsMember2025-01-012025-03-310001612940ifrs-full:IssuedCapitalMember2025-01-012025-03-310001612940ifrs-full:IssuedCapitalMember2024-01-012024-03-310001612940prqr:UnderwritersOptionInConnectionToOctober2024UnderwrittenPublicOfferingMember2024-10-312024-10-310001612940prqr:AtMarketOfferingsWithCantorFitzgeraldAndCoUnderShelfRegistrationStatementMember2024-01-012024-12-310001612940prqr:RettSyndromeResearchTrustMember2024-01-012024-12-310001612940prqr:UnderwritersOptionInConnectionToOctober2024UnderwrittenPublicOfferingMember2024-10-012024-10-310001612940prqr:InnovationCreditMember2025-01-310001612940prqr:InnovationCreditMember2023-12-310001612940ifrs-full:OrdinarySharesMember2024-12-310001612940prqr:OfficeAndLaboratoryFacilitiesAtZernikedreefInLeidenNetherlandsMember2025-03-310001612940prqr:OfficeAndLaboratoryFacilitiesAtZernikedreefInLeidenNetherlandsMember2024-12-310001612940prqr:InnovationCreditMember2023-10-012023-12-310001612940prqr:RettSyndromeResearchTrustMember2025-01-012025-03-310001612940prqr:EliLillyAndCompanyMemberprqr:MilestonePaymentsMember2023-02-012023-02-280001612940prqr:EliLillyAndCompanyMember2021-10-012021-10-310001612940prqr:ProqrTherapeuticsViiiB.v.Member2025-01-012025-03-310001612940prqr:ProqrTherapeuticsViiB.v.Member2025-01-012025-03-310001612940prqr:ProqrTherapeuticsViB.v.Member2025-01-012025-03-310001612940prqr:ProqrTherapeuticsVB.v.Member2025-01-012025-03-310001612940prqr:ProqrTherapeuticsIxB.v.Member2025-01-012025-03-310001612940prqr:ProqrTherapeuticsIvB.v.Member2025-01-012025-03-310001612940prqr:ProqrTherapeuticsIInc.Member2025-01-012025-03-310001612940prqr:ProqrTherapeuticsIiiB.v.Member2025-01-012025-03-310001612940prqr:ProqrTherapeuticsIiB.v.Member2025-01-012025-03-310001612940prqr:ProqrTherapeuticsIB.v.Member2025-01-012025-03-310001612940prqr:ProqrTherapeuticsHoldingB.v.Member2025-01-012025-03-310001612940prqr:SharePurchaseAgreementWithEliLillyAndCompanyMember2024-10-252024-10-250001612940prqr:EliLillyAndCompanyMember2022-12-012022-12-310001612940prqr:EliLillyAndCompanyMember2021-09-012021-09-300001612940prqr:October2024UnderwrittenPublicOfferingMember2024-10-012024-10-310001612940ifrs-full:ReserveOfExchangeDifferencesOnTranslationMember2025-01-012025-03-310001612940ifrs-full:ReserveOfExchangeDifferencesOnTranslationMember2024-01-012024-03-310001612940ifrs-full:PreferenceSharesMember2025-03-310001612940ifrs-full:OrdinarySharesMember2025-03-310001612940prqr:InnovationCreditMember2018-10-120001612940prqr:InnovationCreditMember2025-03-310001612940prqr:InnovationCreditMember2024-12-310001612940ifrs-full:SharePremiumMember2025-01-012025-03-310001612940ifrs-full:RetainedEarningsMember2025-01-012025-03-310001612940ifrs-full:ReserveOfSharebasedPaymentsMember2025-01-012025-03-310001612940ifrs-full:EquityAttributableToOwnersOfParentMember2025-01-012025-03-310001612940ifrs-full:SharePremiumMember2024-01-012024-03-310001612940ifrs-full:RetainedEarningsMember2024-01-012024-03-310001612940ifrs-full:ReserveOfSharebasedPaymentsMember2024-01-012024-03-310001612940ifrs-full:EquityAttributableToOwnersOfParentMember2024-01-012024-03-310001612940prqr:YarrowBiotechnologyMember2025-03-310001612940prqr:PhoenicisTherapeuticsIncMember2025-03-310001612940prqr:YarrowBiotechnologyMember2024-12-310001612940prqr:PhoenicisTherapeuticsIncMember2024-12-310001612940prqr:IfrsSellingGeneralAndAdministrativeExpensesMember2025-01-012025-03-310001612940prqr:IfrsResearchAndDevelopmentExpenseMember2025-01-012025-03-310001612940prqr:IfrsSellingGeneralAndAdministrativeExpensesMember2024-01-012024-03-310001612940prqr:IfrsResearchAndDevelopmentExpenseMember2024-01-012024-03-310001612940ifrs-full:SharePremiumMember2025-03-310001612940ifrs-full:RetainedEarningsMember2025-03-310001612940ifrs-full:ReserveOfSharebasedPaymentsMember2025-03-310001612940ifrs-full:ReserveOfExchangeDifferencesOnTranslationMember2025-03-310001612940ifrs-full:IssuedCapitalMember2025-03-310001612940ifrs-full:EquityAttributableToOwnersOfParentMember2025-03-310001612940ifrs-full:SharePremiumMember2024-12-310001612940ifrs-full:RetainedEarningsMember2024-12-310001612940ifrs-full:ReserveOfSharebasedPaymentsMember2024-12-310001612940ifrs-full:ReserveOfExchangeDifferencesOnTranslationMember2024-12-310001612940ifrs-full:IssuedCapitalMember2024-12-310001612940ifrs-full:EquityAttributableToOwnersOfParentMember2024-12-310001612940ifrs-full:SharePremiumMember2024-03-310001612940ifrs-full:RetainedEarningsMember2024-03-310001612940ifrs-full:ReserveOfSharebasedPaymentsMember2024-03-310001612940ifrs-full:ReserveOfExchangeDifferencesOnTranslationMember2024-03-310001612940ifrs-full:IssuedCapitalMember2024-03-310001612940ifrs-full:EquityAttributableToOwnersOfParentMember2024-03-310001612940ifrs-full:SharePremiumMember2023-12-310001612940ifrs-full:RetainedEarningsMember2023-12-310001612940ifrs-full:ReserveOfSharebasedPaymentsMember2023-12-310001612940ifrs-full:ReserveOfExchangeDifferencesOnTranslationMember2023-12-310001612940ifrs-full:IssuedCapitalMember2023-12-310001612940ifrs-full:EquityAttributableToOwnersOfParentMember2023-12-310001612940prqr:EliLillyAndCompanyMember2021-09-300001612940prqr:RettSyndromeResearchTrustMember2025-03-310001612940prqr:EliLillyAndCompanyMember2025-03-310001612940prqr:RettSyndromeResearchTrustMember2024-12-310001612940prqr:EliLillyAndCompanyMember2024-12-3100016129402024-03-3100016129402023-12-3100016129402024-01-012024-03-3100016129402025-03-3100016129402024-12-3100016129402025-01-012025-03-31iso4217:EURxbrli:sharesiso4217:EURxbrli:sharesiso4217:USDxbrli:pureutr:sqmprqr:segmentiso4217:USDxbrli:shares

Table of Contents

PAGE 1

Unaudited Condensed Consolidated Financial Statements

PROQR THERAPEUTICS N.V.
Unaudited Condensed Consolidated Statement of Financial Position

March 31, 

December 31, 

2025

2024

€1,000

€1,000

Assets

  

  

Property, plant and equipment

7

13,608

14,113

Investments in financial assets

17

Non-current assets

13,608

14,113

Cash and cash equivalents

5

132,414

149,408

Prepayments and other receivables

6

5,137

3,747

Other taxes

530

690

Current assets

138,081

153,845

Total assets

151,689

167,958

Equity and liabilities

  

  

Equity

  

Equity attributable to owners of the Company

78,935

88,560

Total equity

12

78,935

88,560

Liabilities

  

  

Borrowings

9

Lease liabilities

10

10,738

11,067

Deferred income

11

28,299

29,429

Non-current liabilities

39,037

40,496

Borrowings

9

4,655

4,582

Lease liabilities

10

1,460

1,567

Derivative financial instruments

9

186

468

Trade payables

414

16

Social securities and other taxes

481

1,478

Deferred income

11

19,250

21,942

Other current liabilities

8

7,271

8,849

Current liabilities

33,717

38,902

Total liabilities

72,754

79,398

Total equity and liabilities

151,689

167,958

The accompanying notes are an integral part of these unaudited interim condensed consolidated financial statements.

Table of Contents

PAGE 2

Unaudited Condensed Consolidated Financial Statements

PROQR THERAPEUTICS N.V.
Unaudited Condensed Consolidated Statement of Profit or Loss and Other Comprehensive Income

(€ in thousands, except share and per share data)

Three month period

ended March 31, 

    

2025

2024

€1,000

€1,000

Revenue

13

4,519

4,450

Other income

14

222

210

Research and development costs

15

(12,323)

(9,283)

General and administrative costs

16

(3,234)

(3,452)

Total operating costs

(15,557)

(12,735)

  

  

Operating result

(10,816)

(8,075)

Finance income and expense

455

488

Results related to financial liabilities measured at fair value through profit or loss

9

282

(68)

  

  

Result before corporate income taxes

(10,079)

(7,655)

Income taxes

18

(3)

  

  

Result for the period

(10,079)

(7,658)

Other comprehensive income (foreign exchange differences on foreign operation)

(371)

191

  

  

Total comprehensive income

(10,450)

(7,467)

Result attributable to

  

  

Owners of the Company

(10,079)

(7,658)

Non-controlling interests

(10,079)

(7,658)

Total comprehensive income attributable to

Owners of the Company

(10,450)

(7,467)

Non-controlling interests

(10,450)

(7,467)

  

  

Share information

  

  

Weighted average number of shares outstanding1

105,296,833

81,571,028

Earnings per share attributable to owners of the Company (Euro per share)

Basic loss per share1

(0.10)

(0.09)

Diluted loss per share1

(0.10)

(0.09)

The accompanying notes are an integral part of these unaudited interim condensed consolidated financial statements.

1.For these periods the potential exercise of share options is not included in the diluted earnings per share as the Company was loss-making. Due to the anti-dilutive nature of the outstanding options, basic and diluted earnings per share are equal.

Table of Contents

PAGE 3

Unaudited Condensed Consolidated Financial Statements

PROQR THERAPEUTICS N.V.
Unaudited Condensed Consolidated Statement of Changes in Equity

Attributable to owners of the Company

  

Number
of shares

  

Share
Capital

  

Share
Premium

  

Equity settled
Employee
Benefit
Reserve

  

Translation
Reserve

  

Accumulated
Deficit

  

Total

  

Non-
controlling
interests

  

Total
Equity

 

  

€1,000

€1,000

€1,000

€1,000

€1,000

€1,000

€1,000

€1,000

Balance at January 1, 2024

 

84,248,384

3,370

412,894

25,159

817

(400,850)

41,390

41,390

Result for the period

 

(7,658)

(7,658)

(7,658)

Other comprehensive income

 

191

191

191

Recognition of share-based payments

 

736

736

736

Treasury shares transferred

(307,627)

Share options lapsed

(40)

40

Share options exercised / RSUs vested

307,627

162

(278)

278

162

162

Balance at March 31, 2024

 

84,248,384

3,370

413,056

25,577

1,008

(408,190)

34,821

34,821

Balance at January 1, 2025

 

107,710,916

4,308

483,812

26,248

1,350

(427,158)

88,560

88,560

Result for the period

 

(10,079)

(10,079)

(10,079)

Other comprehensive income

 

(371)

(371)

(371)

Recognition of share-based payments

 

758

758

758

Treasury shares transferred

(130,436)

Share options lapsed

(826)

826

Share options exercised / RSUs vested

130,436

67

(180)

180

67

67

 

  

  

  

  

  

  

  

  

  

Balance at March 31, 2025

 

107,710,916

4,308

483,879

26,000

979

(436,231)

78,935

78,935

The accompanying notes are an integral part of these unaudited interim condensed consolidated financial statements.

Table of Contents

PAGE 4

Unaudited Condensed Consolidated Financial Statements

PROQR THERAPEUTICS N.V.
Unaudited Condensed Consolidated Statement of Cash Flows

Three month period 

ended March 31, 

    

2025

2024

€1.000

€1.000

Cash flows from operating activities

  

  

Net result

(10,079)

(7,658)

Adjustments for:

— Other income

(222)

— Depreciation

678

691

— Share-based compensation

758

736

— Financial income and expenses

(508)

(488)

— Results related to financial liabilities measured at fair value through profit or loss

(282)

68

— Income tax expenses

18

3

Changes in working capital

(6,721)

(9,224)

Cash used in operations

(16,376)

(15,872)

  

  

Corporate income tax paid

(3)

Interest received

788

932

Interest paid

(210)

(189)

  

  

Net cash used in operating activities

(15,798)

(15,132)

  

  

Cash flow from investing activities

Increase in financial asset - current

(17,000)

Purchases of property, plant and equipment

(224)

(732)

  

  

Net cash used in investing activities

(224)

(17,732)

  

  

Cash flow from financing activities

  

  

Proceeds from exercise of share options

12

67

162

Repayment of lease liability

10

(567)

(581)

  

  

Net cash used in financing activities

(500)

(419)

  

  

Net decrease in cash and cash equivalents

(16,522)

(33,283)

  

  

Currency effect cash and cash equivalents

(472)

71

Cash and cash equivalents at beginning of the period

5

149,408

118,925

  

  

Cash and cash equivalents at the end of the period

132,414

85,713

The accompanying notes are an integral part of these unaudited interim condensed consolidated financial statements.

Table of Contents

PAGE 5

Unaudited Condensed Consolidated Financial Statements

PROQR THERAPEUTICS N.V.
Notes to Unaudited Condensed Consolidated Financial Statements

1. General Information

ProQR Therapeutics N.V., or “ProQR” or the “Company”, is a biotechnology company domiciled in the Netherlands that primarily focuses on the discovery and development of novel therapeutic medicines.

Since September 18, 2014, the Company’s ordinary shares have been listed on Nasdaq. They are currently trading at Nasdaq Capital Market under ticker symbol PRQR.

The Company was incorporated in the Netherlands, on February 21, 2012 (Chamber of Commerce no. 54600790) and was reorganized from a private company with limited liability to a public company with limited liability on September 23, 2014. The Company has its statutory seat in Leiden, the Netherlands. The address of its headquarters and registered office is Zernikedreef 9, 2333 CK Leiden, the Netherlands.

ProQR Therapeutics N.V. is the ultimate parent company of the following entities:

ProQR Therapeutics Holding B.V. (100%);
ProQR Therapeutics I B.V. (100%);
ProQR Therapeutics II B.V. (100%);
ProQR Therapeutics III B.V. (100%);
ProQR Therapeutics IV B.V. (100%);
ProQR Therapeutics V B.V. (100%);
ProQR Therapeutics VI B.V. (100%);
ProQR Therapeutics VII B.V. (100%);
ProQR Therapeutics VIII B.V. (100%);
ProQR Therapeutics IX B.V. (100%);
ProQR Therapeutics I Inc. (100%)

ProQR Therapeutics N.V. is also statutory director of Stichting Bewaarneming Aandelen ProQR (“ESOP Foundation”) and has full control over this entity.

As used in these condensed consolidated financial statements, unless the context indicates otherwise, all references to “ProQR” or the “Company” refer to ProQR Therapeutics N.V. including its subsidiaries and the ESOP Foundation.

Table of Contents

PAGE 6

Unaudited Condensed Consolidated Financial Statements

2. Significant Accounting Policies

These interim condensed consolidated financial statements for the three month period ended March 31, 2025 have been prepared in accordance with IAS 34 Interim Financial Statements. They should be read in conjunction with the Company’s annual financial statements for the year ended December 31, 2024. These interim condensed consolidated financial statements do not include all information required for a complete set of financial statements prepared in accordance with IFRS Standards. However, selected explanatory notes are included to explain events and transactions that are significant to an understanding of the changes in the Company’s financial position and performance since the last annual financial statements. In the opinion of management, all events and transactions that are significant to an understanding of the changes in financial position and performance of the Company since the end of the last annual reporting period are disclosed in these interim condensed consolidated financial statements. The accounting policies adopted in the preparation of the interim condensed consolidated financial statements are consistent with those applied in the preparation of the Company’s annual financial statements for the year ended December 31, 2024.

During the quarter ended March 31, 2024, the Company invested in financial assets in the form of deposits with an original maturity of longer than three months but shorter than twelve months which are measured at amortized cost as they give rise on specified dates to cash flows that are solely payments of principal and interest on the principal amount outstanding.

The Company’s financial results have varied substantially, and are expected to continue to vary, from period to period. The Company believes that its ordinary activities are not linked to any particular seasonal factors.

The management of ProQR has, upon preparing and finalizing these interim condensed consolidated financial statements, assessed the Company’s ability to fund its operations for a period of at least one year after the date of signing these interim condensed consolidated financial statements. Management expects the Company to continue as a going concern based on its existing funding, taking into account the Company’s current cash position and the projected cash flows based on the activities under execution on the basis of ProQR’s business plan and budget. Thus, we continue to adopt the going concern basis of accounting in preparing the interim condensed consolidated financial statements.

The carrying amount of all financial assets and financial liabilities is a reasonable approximation of the fair value and therefore, information about the fair values of each class has not been disclosed.

The Company operates in one reportable segment, which comprises the discovery and development of innovative, RNA based therapeutics.

3. Adoption of New and Revised International Financial Reporting Standards

New Standards and Interpretations, which became effective as of January 1, 2025, did not have a material impact on our condensed consolidated financial statements.

Table of Contents

PAGE 7

Unaudited Condensed Consolidated Financial Statements

4. Critical Accounting Estimates and Judgements

In the application of the Company’s accounting policies, management is required to make judgments, estimates and assumptions about the carrying amounts of assets and liabilities that are not readily apparent from other sources. The estimates and associated assumptions are based on historical experience and other factors that are considered to be relevant. Actual results may differ from these estimates.

The estimates and underlying assumptions are reviewed on an ongoing basis. Revisions to accounting estimates are recognized in the period in which the estimate is revised if the revision affects only that period or in the period of the revision and future periods if the revision affects both current and future periods.

The significant judgements made by management in applying the Company’s accounting policies and the key sources of estimation uncertainty were the same as those described in the Company’s annual financial statements for the year ended December 31, 2024.

(i) Revenue recognition for the Eli Lilly and Company research and collaboration agreement

a. Identification of the performance obligations

As further described in Note 13 the identification of the performance obligations for the Company’s original research and collaboration agreement with Eli Lilly and Company (“Lilly”), and the amended and restated research and collaboration agreement (collectively, the “Collaboration agreement”) involves significant judgement.

A key judgement was made in determining that the license granted to Lilly is not distinct from the associated research and development (“R&D”) services, due to the lack of stand-alone value of the license without the Company’s involvement and the significant interdependencies between the license and the R&D services to be provided by the Company. As a result, the license and the R&D services are accounted for together as a single combined performance obligation consisting of multiple activities that are not distinct.

b. Determining the timing of satisfaction of performance obligations

As further described in Note 13, before the handover of a compound to Lilly, the Company recognizes revenue over time, using an input method that estimates the satisfaction of the performance obligation as the percentage of labor hours incurred compared to the total estimated labor hours required to complete the promised services. As the Company’s estimate of the total labor hours required is dependent on the evolution of the research and development activities, it may be subject to change. If the progression and/or outcome of certain research and development activities would be different from the assumptions that were made during the preparation of these financial statements, this could lead to material adjustments to the total estimated labor hours, which might result in a reallocation of revenue between current and future periods. Our total deferred revenue balance related to this Lilly performance obligation amounts to € 47,329,000 at March 31, 2025 (December 31, 2024: € 50,930,000).

c. Determining the transaction price

The Company applied judgement to determine whether the equity investments made by Lilly in ProQR are part of the transaction price for the Collaboration agreement. The Company concluded that the differences between the prices that Lilly paid for the shares and the ProQR stock closing prices on the days of entering into the equity investment agreements arose because of the Company’s existing obligations to deliver research and development services to Lilly under the terms of the Collaboration agreement. Therefore, the above differences between the closing share prices on the agreement effective dates and the equity investment prices paid by Lilly are considered to be part of the transaction price of the contract and are initially allocated to deferred revenue.

Table of Contents

PAGE 8

Unaudited Condensed Consolidated Financial Statements

The contract also includes variable consideration, but no variable consideration was included in the initial transaction price at the inception, as it is not highly probable that a significant reversal in the amount of cumulative revenue recognized will not occur. The Company includes such variable consideration in the transaction price when the uncertainty associated with the variable consideration is resolved.

The Collaboration agreement includes variable consideration in the form of development milestones, commercial milestones, and sales-based royalties based on the level of sales. As further described in Note 13, during March 31, 2025 the Company achieved development milestones during the ProQR research program under the agreement, which were added to the transaction price and recognized partially as revenue during 2025 based on the status of completion (satisfied part) of the single combined performance obligation.

(ii) Research and development expenditures

Research expenditures are reflected in the income statement. Development expenses are currently also reflected in the income statement because the criteria for capitalization are not met. At each balance sheet date, the Company estimates the level of service performed by the vendors and the associated costs incurred for the services performed.

Although we do not expect the estimates to be materially different from amounts actually incurred, the understanding of the status and timing of services performed relative to the actual status and timing of services performed may vary and could result in reporting amounts that are too high or too low in any particular period.

5. Cash and Cash Equivalents

At March 31, 2025, the Company’s cash and cash equivalents were € 132,414,000 compared to € 149,408,000 at December 31, 2024. The cash balances are held at banks with investment grade credit ratings. Short-term credit ratings must be rated A-1/P-1/F1 at a minimum by at least one of the Nationally Recognized Statistical Rating Organizations (“NRSROs”) specifically Moody’s, Standard & Poor’s or Fitch. The cash at banks is at full disposal of the Company. Included in cash and cash equivalents are deposits fixed for at most 3-month periods at a time.

6. Prepayments and Other Receivables

March 31, 

December 31, 

2025

2024

€1,000

€1,000

Prepayments

2,910

2,410

Other receivables

1,725

835

Accrued income from Rett Syndrome Research Trust

502

502

5,137

3,747

All receivables are considered short-term and due within one year. At March 31, 2025 and December 31, 2024 prepayments consisted principally of payments made by the Company for services not yet provided by vendors. At March 31, 2025 and December 31, 2024 other receivables consisted principally of accrued grant income and deposits. As at March 31, 2025 and December 31, 2024 the accrued grant income relating to Rett Syndrome Research Trust (“RSRT”) includes the initial fair value of the warrants issued to RSRT that was accounted for as a reduction of the transaction price. The RSRT agreement is described in Note 14. Other Income.

Table of Contents

PAGE 9

Unaudited Condensed Consolidated Financial Statements

7. Property, Plant and Equipment

At March 31, 2025 and December 31, 2024, property plant and equipment consisted of buildings and leasehold improvements, laboratory equipment and other assets. Buildings and leasehold improvements include a right-of-use asset relating to the lease of our Leiden office and laboratory space, with a carrying amount of € 11,122,000 at March 31, 2025 (December 31, 2024: € 11,433,000).

8. Other Current Liabilities

At March 31, 2025, other current liabilities amount to € 7,271,000 (December 31, 2024: € 8,849,000). At March 31, 2025 and December 31, 2024, other current liabilities consisted principally of accruals for services provided by vendors not yet billed, payroll related accruals and other miscellaneous liabilities.

9. Borrowings

March 31, 

December 31, 

    

2025

2024

€1,000

€1,000

Innovation credit

2,899

2,899

Accrued interest on innovation credit

1,756

1,683

Total borrowings

4,655

4,582

Current portion

4,655

4,582

Total non-current borrowings

In December 2018, ProQR was awarded an Innovation credit for the sepofarsen program. Amounts were drawn under this facility from 2018 through 2022. The credit of € 3,907,000 was used to conduct the Phase 2/3 clinical study and efforts to obtain regulatory and ethical market approval (New Drug Applications (“NDA”)/ Marketing Authorization Applications (“MAA”)) of sepofarsen for LCA10. In the fourth quarter of 2023, ProQR made a partial repayment of the principal, amounting to € 1,008,000. The remaining amount payable of € 2,899,000 is recognized under current borrowings as at March 31, 2025 and December 31, 2024.

In December 2023, ProQR received a waiver for the remaining balance of the Innovation credit including accrued interest. As a result, the repayment of the total loan of € 4,292,000, including accrued interest, could be waived if conditions are met, subject to annual review. In January 2025, the waiver for the total balance of € 4,582,000, including interest, was again extended until December 31, 2025.

In September 2022, ProQR extinguished its debt with Pontifax and Kreos by repaying all outstanding principal amounts. Pontifax’ and Kreos’ warrants remain in place until their five-year economic life expires in 2025 and 2026. These warrants are accounted for as embedded derivatives and were recognized separately from the host contract as derivative financial liabilities at fair value through profit or loss.

10. Lease Liabilities

At March 31, 2025 and December 31, 2024, lease liabilities primarily consisted of the Company’s lease of office and laboratory facilities at Zernikedreef in Leiden, the Netherlands.

The Company leases office and laboratory facilities of 4,818 square meters at Zernikedreef in Leiden, the Netherlands, where our headquarters and our laboratories are located. The current lease agreement for these facilities terminates on June 30, 2031. The lease agreement contains no significant dismantling requirements.

Table of Contents

PAGE 10

Unaudited Condensed Consolidated Financial Statements

The initial 10-year lease agreement for the Leiden office and laboratory facilities was accounted for as of commencement date July 1, 2020. This 10-year period was extended by 1 year to an 11-year period in December 2020. The lease contract may be extended for subsequent 5-year periods. As the Company is not reasonably certain to exercise these extension options, these are not included in the lease term.

The carrying amount of the right-of-use asset is disclosed in Note 7.

11. Deferred Income

The following table summarizes details of deferred income at March 31, 2025 and December 31, 2024. The nature of the deferred income is described in Note 13 and 14.

March 31, 

December 31, 

2025

2024

€1,000

€1,000

Payments from Eli Lilly and Company

19,030

21,501

Payments from Rett Syndrome Research Trust

220

441

Current deferred income

19,250

21,942

Payments from Eli Lilly and Company

28,299

29,429

Non-current deferred income

28,299

29,429

Total deferred income

47,549

51,371

c

12. Shareholders’ Equity

The authorized share capital of the Company amounting to € 13,600,000 consists of 170,000,000 ordinary shares and 170,000,000 preference shares with a par value of € 0.04 per share. At March 31, 2025, 107,710,916 ordinary shares were issued. 105,342,963 ordinary shares were fully paid and 2,367,953 ordinary shares were held by the Company as treasury shares (December 31, 2024: 2,498,389).

In September 2024, the Company filed a shelf registration statement on Form F-3, which permitted: (a) the offering, issuance and sale by the Company of up to a maximum aggregate offering price of $ 300,000,000 of its ordinary shares, warrants and/or units; and (b) as part of the $ 300,000,000, the offering, issuance and sale by the Company of up to a maximum aggregate offering price of $ 75,000,000 of its ordinary shares that may be issued and sold under a sales agreement (the “sales agreement”) with Cantor Fitzgerald & Co. (“Cantor”) in one or more at-the-market (“ATM”) offerings. The Company will pay Cantor a commission equal to 3% of the gross proceeds of the sales price of all ordinary shares sold through it as sales agent under the sale agreement. As of December 31, 2024, no shares have been issued pursuant to this ATM facility.

In October 2024, the Company consummated an underwritten public offering of 18,000,000 ordinary shares (the “offering”) at a public offering price of $ 3.50 per share (the “public offering price”). In addition, the Company granted the underwriters a 30-day option to purchase up to 2,700,000 additional ordinary shares at the public offering price, less underwriting discounts and commissions. The option was partially exercised on October 31, 2024, resulting in the issuance of 1,940,072 shares. The gross proceeds from the Offering and subsequent partial exercise of the underwriters’ option, amounted to $ 69,790,000 (€ 64,600,000) while the transaction costs amounted to approximately € 4,365,000, resulting in net proceeds of approximately € 60,235,000.

Table of Contents

PAGE 11

Unaudited Condensed Consolidated Financial Statements

Concurrently with the Offering, the Company entered into a share purchase agreement with Lilly in a separately negotiated transaction (the “concurrent private placement”), pursuant to which the Company agreed to offer and sell, and Lilly agreed to purchase, 3,523,538 ordinary shares at a price per share equal to the public offering price, for total gross proceeds of approximately $ 12,300,000, subject to a purchase price cap of $ 15,000,000, the consummation of the Offering and the satisfaction of other customary closing conditions. The proceeds of $ 12,300,000 million (€ 11,400,000) from the concurrent private placement were received on October 25, 2024. The ordinary shares purchased in the concurrent private placement are not subject to any underwriting discounts or commissions.

Translation reserve

The translation reserve comprises all foreign currency differences arising from the translation of the financial statements of foreign operations.

Share options

The Company operates an equity-settled share-based compensation plan, which was introduced in 2013. Options and Restricted Stock Units (“RSUs”) may be granted to employees, members of the Board and consultants. The compensation expenses included in operating costs for this plan in the three month period ended March 31, 2025 were € 758,000 (three month period ended March 31, 2024: € 736,000), of which € 566,000 was recorded in general and administrative costs (three month period ended March 31, 2024: € 577,000) and € 192,000 was recorded in research and development costs (three month period ended March 31, 2024: € 159,000).

13. Revenue

Eli Lilly and Company collaboration

In September 2021, the Company entered into a global licensing and research collaboration with Lilly focused on the discovery, development, and commercialization of potential new medicines for genetic disorders in the liver and nervous system. ProQR and Lilly will use ProQR’s proprietary Axiomer® RNA editing platform to progress new drug targets toward clinical development and commercialization.

Under the terms of the agreement, ProQR received an upfront payment and equity consideration, and is eligible to receive milestone payments and royalties on the net sales of any resulting products. In September 2021, the Company issued 3,989,976 shares to Lilly, resulting in gross proceeds of 30,000,000 (€ 25,270,000). These shares were issued at a premium of $ 2,429,000 (€ 2,047,000), which was determined to be part of the transaction price and as such was initially recognized as deferred revenue. An up-front payment of $ 20,000,000 (€ 16,849,000) was received in October 2021.

In December 2022, the Company and Lilly amended their research and collaboration agreement described above, which expanded the collaboration. Under the amended and restated research and collaboration agreement, Lilly will gain access to additional targets in the central nervous system (“CNS”) and peripheral nervous system (“PNS”) with ProQR’s Axiomer platform.

As described under Note 12, pursuant to the amended and restated agreement, the Company issued 9,381,586 shares to Lilly in December 2022, resulting in gross proceeds of $ 15,000,000 (€ 14,122,000). These shares were issued at a discount of $ 480,000 (€ 451,000), which is accounted for as a reduction of the transaction price. In February 2023, ProQR also received an upfront payment of $ 60,000,000 (€ 56,412,000). Lilly has the ability to exercise an option to further expand the partnership for a consideration of $ 50,000,000.

Table of Contents

PAGE 12

Unaudited Condensed Consolidated Financial Statements

With regard to the original and amended and restated research and collaboration agreements with Lilly, the Company concluded as follows:

The amended and restated research and collaboration agreement is accounted for as a separate contract under IFRS 15 given the group of promises to be delivered are distinct and are priced commensurate with stand-alone selling prices.
For each of the agreements, the company identified one performance obligation under IFRS 15, for the transfer of a license combined with the performance of research and development activities. The Company concluded that the license is not capable of being distinct and is not distinct in the context of the contract. ProQR’s services are evaluated as predominant at inception of the contract and the compounds resulting from the collaboration do not represent a series of distinct promises because they were not predetermined at the inception of the contract and can be terminated or replaced at the discretion of Lilly subject to the terms and conditions of the Collaboration agreement.
The transaction price of the agreement includes fixed components, consisting of an up-front fee and an equity component (premium or discount). The agreement also contains variable parts, notably milestones, which are included in the transaction price to the extent that it is highly probable that a significant reversal in the amount of cumulative revenue recognized will not occur when the uncertainty associated with the variable consideration is subsequently resolved. Development milestone payments to be reached during the ProQR research program will only be included to the extent that it is highly probable that a significant reversal in the amount of cumulative revenue recognized will not occur when the uncertainty associated with the milestones is subsequently resolved. Sales-based milestones and sales-based royalties will be included as the underlying sales occur.
Initially, the Company recognizes revenue over time, using an input method that estimates the satisfaction of the performance obligation as the percentage of labor hours incurred compared to the total estimated labor hours required to complete the promised services.

After the handover of a compound to Lilly:

The variable consideration for development milestones to be reached during the Lilly R&D activities is linked to a separable right to use the license which comes into existence for each successful compound transferred to Lilly. This license is a separate performance obligation and revenue will be recognized at a point in time when the development milestone for a license is achieved and the variable constraint is resolved.
The variable consideration for commercial milestones is linked to a separable right to use the license which comes into existence for each successful compound transferred to Lilly. This license is a separate performance obligation and will be recognized at a point in time when the commercial milestone for a license is achieved and the variable constraint is resolved.
For sales-based royalties, the license is the predominant item to which the royalty relates. The sales-based royalties will be recognized after the handover of the compound to Lilly (after completion of the initial performance obligation) and once the respective sale level occurs.  

During the three month period ended March 31, 2025, the Company reached milestones amounting to $ 1,000,000 (€ 918,000) under the agreement, which was added to the transaction price and recognized partially as revenue during the three month period ended March 31, 2025.

Table of Contents

PAGE 13

Unaudited Condensed Consolidated Financial Statements

14. Other Income

Three month period

ended March 31, 

    

2025

2024

€1,000

€1,000

Grant income

222

210

222

210

In January, 2024, the Company entered into an agreement with the RSRT that focuses on the design and development of editing oligonucleotides (“EONs”) using the Company’s Axiomer technology platform targeting the transcription factor Methyl CpG binding protein 2 (“MECP2”) and correcting mutations of interest. Under the agreement, RSRT awarded the Company up to € 1,015,000 as a research grant for the initial phase of the project that was received during 2024, out of which € 575,000 was recognized as Other Income during 2024 and the remaining part recorded as Deferred Income. In December 2024, the Company expanded partnership with RSRT to include an additional $ 8,150,000 in funding from the RSRT to support the advancement of the selected candidates into clinical trials. As at March 31, 2025 no amounts have been received under this agreement and the work has not yet commenced.

Grants are recognized in other income in the same period in which the related R&D costs are recognized.

15. Research and Development Costs

Research and development costs amount to € 12,323,000 for the three month period ended March 31, 2025 (three month period ended March 31, 2024: € 9,283,000) and are comprised of allocated employee costs including share-based payments, the costs of materials and laboratory consumables, outsourced activities, license and intellectual property costs and other allocated costs. Research and development costs increased compared to the same period in the prior year, mainly due to the Company’s increased outsourced research and development activities and full time employee equivalents (“FTE”) in the three month period of 2025.

16. General and Administrative Costs

General and administrative costs amount to € 3,234,000 for the three month period ended March 31, 2025 (three month period ended March 31, 2024: € 3,452,000).

17. Investments in Financial Assets

Investment in financial assets consist of the Company’s investment in Phoenicis Therapeutics Inc. (“Phoenicis”) and Yarrow Biotechnology Inc. (“Yarrow”).

ProQR holds a 3.9% interest in Phoenicis. As at March 31, 2025, the investment amounts to € nil (December 31, 2024: € nil). Phoenicis discontinued its operations during the quarter ended September 30, 2024.

ProQR holds a 5.1% interest in Yarrow. As at March 31, 2025, the fair value of the Yarrow financial asset amounted to € nil (December 31, 2024: € nil).

Table of Contents

PAGE 14

Unaudited Condensed Consolidated Financial Statements

18. Income Taxes

The current income tax liability amounts to € nil at March 31, 2025 (December 31, 2024: € nil). No significant temporary differences exist between accounting and tax results. Realization of deferred tax assets is dependent on future earnings, if any, the timing and amount of which are uncertain. Accordingly, the Company has not yet recognized any deferred tax asset related to operating losses.

Tax losses may be carried forward indefinitely. However, the offset of losses will be limited in a given year against the first € 1 million of taxable profit. For taxable profit in excess of this amount, losses may only be offset up to 50% of this excess. In addition, unused non-deductible interest expenses may be carried forward indefinitely. However, the offset will be limited in a given year against the higher of 20% of adjusted taxable profit or € 1.0 million of interest income.

19. Related-Party Transactions

The Company does not have any transactions with related parties other than compensation to its Board members.

20. Events After Balance Sheet Date

None.

Exhibit 99.2

ProQR Announces First Quarter 2025 Operating and Financial Results

Axiomer™ ADAR-mediated RNA editing pipeline advancing across liver and CNS programs, with CTA filing on track for Q2 2025 for lead program AX-0810 targeting NTCP for Cholestatic diseases
Strengthened leadership with appointments of Chief Financial Officer and Chief Medical Officer
€ 132.4 million cash and cash equivalents as of end Q1 providing runway into mid-2027, plus additional potential milestones from Lilly partnership

LEIDEN, Netherlands & CAMBRIDGE, Mass., May 8, 2025 – ProQR Therapeutics N.V. (Nasdaq: PRQR) (ProQR), a company dedicated to changing lives through transformative RNA therapies based on its proprietary Axiomer RNA editing technology platform, today reported its financial and operating results for the first quarter ended March 31, 2025, and provided a business update.

“ProQR entered 2025 in a position of strength, with solid fundamentals, a well-capitalized balance sheet, and a clear focus on execution,” said Daniel A. de Boer, Founder and Chief Executive Officer of ProQR. “We remain on track to submit the CTA for our lead RNA editing program, AX-0810 targeting NTCP for cholestatic diseases, in Q2 2025, with our first clinical data readout expected in Q4 – key milestones for our lead Axiomer pipeline program that we believe will drive significant value for stakeholders. I’m delighted that we further strengthened our leadership team with the recent appointments of Chief Financial Officer Dennis Hom and Chief Medical Officer Dr. Cristina Lopez Lopez, bringing deep financial and translational clinical development expertise to support ProQR’s next phase of growth.”

Recent Progress

In April, ProQR announced the appointments of Dennis Hom as Chief Financial Officer and Cristina Lopez Lopez, MD, PhD as Chief Medical Officer. These key leadership appointments support the advancement of the Company’s Axiomer platform technology and pipeline of RNA editing programs as it enters the clinical stage.
Advancing AX-0810 toward CTA filing, on track for Q2 2025. AX-0810 is ProQR’s lead Axiomer RNA editing pipeline program. By modulating NTCP, AX-0810 aims to reduce bile acid accumulation in hepatocytes and address the root cause of cholestatic liver

diseases. The program remains on track for a Clinical Trial Application (CTA) filing in Q2 2025, with the initial clinical assessment planned in healthy volunteers.
In March, ProQR participated in the RNA Editing Gordon Research Conference in Lucca, Italy, presenting “Developing Axiomer™ RNA Editing Technology Towards Application in Liver and CNS Disease”.
Accepted scientific abstracts underscore ProQR’s leadership in RNA editing. ProQR will present multiple abstracts at the upcoming American Society of Gene & Cell Therapy (ASGCT) Annual Meeting, taking place May 13-17, 2025 in New Orleans. These presentations will highlight the Company’s proprietary Axiomer RNA editing platform and pipeline programs, including:
Oral Presentation (333): “ADAR-Mediated RNA Editing of SLC10A1 (NTCP) as a Therapeutic Approach to Reduce Liver Bile Acid Re-Uptake in Cholestatic Diseases”
Poster Presentation (AMA1324): “ADAR-Mediated RNA Editing-Based Correction of PNPLA3|148M Functionality to Address Hepatic Steatosis”
Poster Presentation (AMA1427): “ADAR-Mediated RNA Editing of Premature Termination Codon Results in Functional Correction in MECP2 for Rett Syndrome

Anticipated Upcoming Events

AX-0810 targeting NTCP for Cholestatic diseases
Q2 2025 Clinical Trial Application (CTA) submission
Q4 2025 first clinical target engagement and biomarker data in healthy volunteers
AX-2402 targeting MECP2 (R270X) for Rett Syndrome
2025 clinical candidate selection
2026 clinical trial initiation and topline data readout
AX-2911 targeting PNPLA3 for MASH
2025 clinical candidate selection
2026 clinical trial initiation and topline data readout
AX-1412 targeting B4GALT1 for Cardiovascular diseases
mid-2025 update on optimization for GalNAc delivery
Continue to execute on partnership with Eli Lilly and Company (Lilly), with potential data updates, milestone income from the existing partnership, and an option to exercise for an additional five targets for expansion to a total of 15 targets, which would result in a $50 million opt-in payment to ProQR.
ProQR may selectively form new partnerships, which could include multi-target discovery alliances, or product alliances on specific programs.

Financial Highlights

At March 31, 2025, ProQR held cash and cash equivalents of € 132.4 million, compared to
€ 149.4 million cash and cash equivalents at December 31, 2024. Net cash used in operating activities during the three-month period ended March 31, 2025 was € 15.8 million, compared to € 15.1 million for the same period last year. During the first quarter of 2025, the Company achieved a milestone in the collaboration agreement with Eli Lilly earning $1.0 million (€ 918,000).

Research and development (R&D) costs were € 12.3 million for the quarter ended March 31, 2025 compared to € 9.3 million for the same period last year.

General and administrative costs were € 3.2 million for the quarter ended March 31, 2025 compared to € 3.5 million for the same period last year.

Net loss for the three-month period ended March 31, 2025 was € 10.1 million, or € 0.10 per diluted share, compared to € 7.7 million, or € 0.09 per diluted share, for the same period last year. For further financial information for the period ended March 31, 2025, please refer to the Q1 financial report filing available on our website, www.proqr.com under Financials and Filings.

About Axiomer™

ProQR is pioneering a next-generation RNA base editing technology called Axiomer, which could potentially yield a new class of medicines for diverse types of diseases. Axiomer “Editing Oligonucleotides”, or EONs, mediate single nucleotide changes to RNA in a highly specific and targeted way using molecular machinery that is present in human cells called ADAR (Adenosine Deaminase Acting on RNA). Axiomer EONs are designed to recruit and direct endogenously expressed ADARs to change an Adenosine (A) to an Inosine (I) in the RNA – an Inosine is translated as a Guanosine (G) – correcting an RNA with a disease-causing mutation back to a normal (wild type) RNA, modulating protein expression, or altering a protein so that it will have a new function that helps prevent or treat disease.

About ProQR

ProQR Therapeutics is dedicated to changing lives through the creation of transformative RNA therapies. ProQR is pioneering a next-generation RNA technology called Axiomer, which uses a cell’s own editing machinery called ADAR to make specific single nucleotide edits in RNA to reverse a mutation or modulate protein expression and could potentially yield a new class of medicines for both rare and prevalent diseases with unmet need.


Based on our unique proprietary RNA repair platform technologies we are growing our pipeline with patients and loved ones in mind.

Learn more about ProQR at www.proqr.com.

Forward Looking Statements

This press release contains forward-looking statements. All statements other than statements of historical fact are forward-looking statements, which are often indicated by terms such as “continue,” "anticipate," "believe," "could," "estimate," "expect," "goal," "intend," "look forward to", "may," "plan," "potential," "predict," "project," "should," "will," "would" and similar expressions. Such forward-looking statements include, but are not limited to, statements regarding our business, technology, strategy, preclinical and clinical model data, our initial pipeline targets and the upcoming strategic priorities and milestones related thereto, the responsibilities, potential strengths and capabilities of our new leadership appointments, the continued advancement of our lead development pipeline programs, including ongoing and planned clinical trials, the anticipated timing of initial clinical data readouts across multiple programs in 2025 and 2026, and the filing of a CTA application for our lead program, AX-0810, in Q2 2025, our Axiomer platform, including the continued development and advancement of our Axiomer platform, the therapeutic potential of our Axiomer RNA editing oligonucleotides and product candidates, the timing, progress and results of our preclinical studies and other development activities, including the release of data related thereto, our patent estate, including our anticipated strength and our continued investment in it, as well as the timing of our clinical development, the potential of our technologies and product candidates, the collaboration with Lilly and the intended benefits thereof, including timing for data updates, potential milestones, exercise of an option to expand targets and the receipt of an opt-in payment, our ability to selectively form new partnerships and enter into future collaborations, and our financial position and cash-runway. Forward-looking statements are based on management's beliefs and assumptions and on information available to management only as of the date of this press release. Our actual results could differ materially from those expressed or implied by these forward-looking statements for many reasons, including, without limitation, the risks, uncertainties and other factors in our filings made with the Securities and Exchange Commission, including certain sections of our most recent annual report filed on Form 20-F. These risks and uncertainties include, among others, the cost, timing and results of preclinical studies and clinical trials and other development activities by us and our collaborative partners whose operations and activities may be slowed or halted shortage and pressure on supply and logistics on the global market, economic sanctions and international tariffs; the likelihood of our preclinical and clinical programs being initiated


and executed on timelines provided and reliance on our contract research organizations and predictability of timely enrollment of subjects and patients to advance our clinical trials and maintain their own operations; our reliance on contract manufacturers to supply materials for research and development and the risk of supply interruption from a contract manufacturer; the potential for future data to alter initial and preliminary results of early-stage clinical trials; the unpredictability of the duration and results of the regulatory review of applications or clearances that are necessary to initiate and continue to advance and progress our clinical programs; the ability to secure, maintain and realize the intended benefits of collaborations with partners, including the collaboration with Lilly; the possible impairment of, inability to obtain, and costs to obtain intellectual property rights; possible safety or efficacy concerns that could emerge as new data are generated in research and development; general business, operational, financial and accounting risks, and risks related to litigation and disputes with third parties; and risks related to macroeconomic conditions and market volatility resulting from global economic developments, geopolitical events and conflicts, high inflation, rising interest rates, tariffs and potential for significant changes in U.S. policies and regulatory environment. Given these risks, uncertainties and other factors, you should not place undue reliance on these forward-looking statements, and we assume no obligation to update these forward-looking statements, even if new information becomes available in the future, except as required by law.

ProQR Therapeutics N.V.

Investor and media contact:
Sarah Kiely
ProQR Therapeutics N.V.
T: +1 617 599 6228
skiely@proqr.com
or

Investor contact:

Peter Kelleher
LifeSci Advisors
T: +1 617 430 7579
pkelleher@lifesciadvisors.com


Financial Tables

PROQR THERAPEUTICS N.V.
Unaudited Condensed Consolidated Statement of Financial Position

March 31, 

December 31, 

2025

2024

€1,000

€1,000

Assets

  

  

Property, plant and equipment

13,608

14,113

Investments in financial assets

Non-current assets

13,608

14,113

Cash and cash equivalents

132,414

149,408

Prepayments and other receivables

5,137

3,747

Other taxes

530

690

Current assets

138,081

153,845

Total assets

151,689

167,958

Equity and liabilities

  

  

Equity

  

Equity attributable to owners of the Company

78,935

88,560

Total equity

78,935

88,560

Liabilities

  

  

Borrowings

Lease liabilities

10,738

11,067

Deferred income

28,299

29,429

Non-current liabilities

39,037

40,496

Borrowings

4,655

4,582

Lease liabilities

1,460

1,567

Derivative financial instruments

186

468

Trade payables

414

16

Social securities and other taxes

481

1,478

Deferred income

19,250

21,942

Other current liabilities

7,271

8,849

Current liabilities

33,717

38,902

Total liabilities

72,754

79,398

Total equity and liabilities

151,689

167,958


PROQR THERAPEUTICS N.V.
Unaudited Condensed Consolidated Statement of Profit or Loss and OCI

(€ in thousands, except share and per share data)

Three month period

ended March 31, 

    

2025

2024

€1,000

€1,000

Revenue

4,519

4,450

Other income

222

210

Research and development costs

(12,323)

(9,283)

General and administrative costs

(3,234)

(3,452)

Total operating costs

(15,557)

(12,735)

  

  

Operating result

(10,816)

(8,075)

Finance income and expense

455

488

Results related to financial liabilities measured at fair value through profit or loss

282

(68)

  

  

Result before corporate income taxes

(10,079)

(7,655)

Income taxes

(3)

  

  

Result for the period

(10,079)

(7,658)

Other comprehensive income (foreign exchange differences on foreign operation)

(371)

191

  

  

Total comprehensive income

(10,450)

(7,467)

Result attributable to

  

  

Owners of the Company

(10,079)

(7,658)

Non-controlling interests

(10,079)

(7,658)

Total comprehensive income attributable to

Owners of the Company

(10,450)

(7,467)

Non-controlling interests

(10,450)

(7,467)

  

  

Share information

  

  

Weighted average number of shares outstanding1

105,296,833

81,571,028

Earnings per share attributable to owners of the Company (Euro per share)

Basic loss per share1

(0.10)

(0.09)

Diluted loss per share1

(0.10)

(0.09)

1.For these periods the potential exercise of share options is not included in the diluted earnings per share as the Company was loss-making. Due to the anti-dilutive nature of the outstanding options, basic and diluted earnings per share are equal.


PROQR THERAPEUTICS N.V.
Unaudited Condensed Consolidated Statement of Changes in Equity

Attributable to owners of the Company

  

Number
of shares

  

Share
Capital

  

Share
Premium

  

Equity settled
Employee
Benefit
Reserve

  

Translation
Reserve

  

Accumulated
Deficit

  

Total

  

Non-
controlling
interests

  

Total
Equity

 

  

€1,000

€1,000

€1,000

€1,000

€1,000

€1,000

€1,000

€1,000

Balance at January 1, 2024

 

84,248,384

3,370

412,894

25,159

817

(400,850)

41,390

41,390

Result for the period

 

(7,658)

(7,658)

(7,658)

Other comprehensive income

 

191

191

191

Recognition of share-based payments

 

736

736

736

Treasury shares transferred

(307,627)

Share options lapsed

(40)

40

Share options exercised / RSUs vested

307,627

162

(278)

278

162

162

Balance at March 31, 2024

 

84,248,384

3,370

413,056

25,577

1,008

(408,190)

34,821

34,821

Balance at January 1, 2025

 

107,710,916

4,308

483,812

26,248

1,350

(427,158)

88,560

88,560

Result for the period

 

(10,079)

(10,079)

(10,079)

Other comprehensive income

 

(371)

(371)

(371)

Recognition of share-based payments

 

758

758

758

Treasury shares transferred

(130,436)

Share options lapsed

(826)

826

Share options exercised / RSUs vested

130,436

67

(180)

180

67

67

 

  

  

  

  

  

  

  

  

  

Balance at March 31, 2025

 

107,710,916

4,308

483,879

26,000

979

(436,231)

78,935

78,935


PROQR THERAPEUTICS N.V.
Unaudited Condensed Consolidated Statement of Cash Flows

Three month period 

ended March 31, 

    

2025

2024

€1,000

€1,000

Cash flows from operating activities

  

  

Net result

(10,079)

(7,658)

Adjustments for:

— Other income

(222)

— Depreciation

678

691

— Share-based compensation

758

736

— Financial income and expenses

(508)

(488)

— Results related to financial liabilities measured at fair value through profit or loss

(282)

68

— Income tax expenses

3

Changes in working capital

(6,721)

(9,224)

Cash used in operations

(16,376)

(15,872)

  

  

Corporate income tax paid

(3)

Interest received

788

932

Interest paid

(210)

(189)

  

  

Net cash used in operating activities

(15,798)

(15,132)

  

  

Cash flow from investing activities

Increase in financial asset - current

(17,000)

Purchases of property, plant and equipment

(224)

(732)

  

  

Net cash used in investing activities

(224)

(17,732)

  

  

Cash flow from financing activities

  

  

Proceeds from exercise of share options

67

162

Repayment of lease liability

(567)

(581)

  

  

Net cash used in financing activities

(500)

(419)

  

  

Net decrease in cash and cash equivalents

(16,522)

(33,283)

  

  

Currency effect cash and cash equivalents

(472)

71

Cash and cash equivalents at beginning of the period

149,408

118,925

  

  

Cash and cash equivalents at the end of the period

132,414

85,713


v3.25.1
Document and Entity Information
3 Months Ended
Mar. 31, 2025
Document and Entity Information [Abstract]  
Document Type 6-K
Document Period End Date Mar. 31, 2025
Current Fiscal Year End Date --12-31
Entity Registrant Name ProQR Therapeutics N.V.
Document Fiscal Year Focus 2025
Document Fiscal Period Focus Q1
Entity Central Index Key 0001612940
Amendment Flag false
v3.25.1
Unaudited Condensed Consolidated Statement of Financial Position - EUR (€)
€ in Thousands
Mar. 31, 2025
Dec. 31, 2024
Assets    
Property, plant and equipment € 13,608 € 14,113
Non-current assets 13,608 14,113
Cash and cash equivalents 132,414 149,408
Prepayments and other receivables 5,137 3,747
Other taxes 530 690
Current assets 138,081 153,845
Total assets 151,689 167,958
Equity    
Equity attributable to owners of the Company 78,935 88,560
Total equity 78,935 88,560
Liabilities    
Lease liabilities 10,738 11,067
Deferred income 28,299 29,429
Non-current liabilities 39,037 40,496
Borrowings 4,655 4,582
Lease liabilities 1,460 1,567
Derivative financial instruments 186 468
Trade payables 414 16
Social securities and other taxes 481 1,478
Deferred income 19,250 21,942
Other current liabilities 7,271 8,849
Current liabilities 33,717 38,902
Total liabilities 72,754 79,398
Total equity and liabilities € 151,689 € 167,958
v3.25.1
Unaudited Condensed Consolidated Statement of Profit or Loss and Other Comprehensive Income - EUR (€)
€ in Thousands
3 Months Ended
Mar. 31, 2025
Mar. 31, 2024
Unaudited Condensed Consolidated Statement of Profit or Loss and Other Comprehensive Income    
Revenue € 4,519 € 4,450
Other income 222 210
Research and development costs (12,323) (9,283)
General and administrative costs (3,234) (3,452)
Total operating costs (15,557) (12,735)
Operating result (10,816) (8,075)
Finance income and expense 455 488
Results related to financial liabilities measured at fair value through profit or loss 282 (68)
Result before corporate income taxes (10,079) (7,655)
Income taxes   (3)
Result for the period (10,079) (7,658)
Other comprehensive income (foreign exchange differences on foreign operation) (371) 191
Total comprehensive loss (10,450) (7,467)
Result attributable to    
Owners of the Company (10,079) (7,658)
Result for the period (10,079) (7,658)
Total comprehensive income attributable to    
Owners of the Company (10,450) (7,467)
Total comprehensive loss € (10,450) € (7,467)
Share information    
Weighted average number of shares outstanding (basic) 105,296,833 81,571,028
Weighted average number of shares outstanding (diluted) 105,296,833 81,571,028
Earnings per share for result attributable to the equity holders of the Company (Euro per share)    
Basic loss per share € (0.1) € (0.09)
Diluted loss per share € (0.1) € (0.09)
v3.25.1
Unaudited Condensed Consolidated Statement of Changes in Equity - EUR (€)
€ in Thousands
Share capital
Share Premium
Equity Settled Employee Benefit Reserve
Translation Reserve
Accumulated Deficit
Total
Total
Balance at beginning of period at Dec. 31, 2023 € 3,370 € 412,894 € 25,159 € 817 € (400,850) € 41,390 € 41,390
Balance at beginning of period (in shares) at Dec. 31, 2023 84,248,384            
Result for the year         (7,658) (7,658) (7,658)
Other comprehensive income (loss)       191   191 191
Recognition of share-based payments     736     736 736
Treasury shares transferred (in shares) (307,627)            
Shares options lapsed     (40)   40    
Shares options exercised / RSUs vested   162 (278)   278 162 162
Share options exercised / RSUs vested (in shares) 307,627            
Balance at end of period at Mar. 31, 2024 € 3,370 413,056 25,577 1,008 (408,190) 34,821 34,821
Balance at end of period (in shares) at Mar. 31, 2024 84,248,384            
Balance at beginning of period at Dec. 31, 2023 € 3,370 412,894 25,159 817 (400,850) 41,390 41,390
Balance at beginning of period (in shares) at Dec. 31, 2023 84,248,384            
Balance at end of period at Dec. 31, 2024 € 4,308 483,812 26,248 1,350 (427,158) 88,560 88,560
Balance at end of period (in shares) at Dec. 31, 2024 107,710,916            
Result for the year         (10,079) (10,079) (10,079)
Other comprehensive income (loss)       (371)   (371) (371)
Recognition of share-based payments     758     758 758
Treasury shares transferred (in shares) (130,436)            
Shares options lapsed     (826)   826    
Shares options exercised / RSUs vested   67 (180)   180 67 67
Share options exercised / RSUs vested (in shares) 130,436            
Balance at end of period at Mar. 31, 2025 € 4,308 € 483,879 € 26,000 € 979 € (436,231) € 78,935 € 78,935
Balance at end of period (in shares) at Mar. 31, 2025 107,710,916            
v3.25.1
Unaudited Condensed Consolidated Statement of Cash Flows - EUR (€)
€ in Thousands
3 Months Ended
Mar. 31, 2025
Mar. 31, 2024
Cash flow from operating activities    
Result for the year € (10,079) € (7,658)
Adjustments for:    
Other income (222)  
Depreciation 678 691
Share-based compensation 758 736
Financial income and expense (508) (488)
Results related to financial liabilities measured at fair value through profit or loss (282) 68
Income tax expenses   3
Changes in working capital (6,721) (9,224)
Cash used in operations (16,376) (15,872)
Corporate income tax paid   (3)
Interest received 788 932
Interest paid (210) (189)
Net cash used in operating activities (15,798) (15,132)
Cash flow from investing activities    
Increase in financial asset - current   (17,000)
Purchases of property, plant and equipment (224) (732)
Net cash used in investing activities (224) (17,732)
Cash flow from financing activities    
Proceeds from exercise of share options 67 162
Repayment of lease liability (567) (581)
Net cash used in financing activities (500) (419)
Net decrease in cash and cash equivalents (16,522) (33,283)
Currency effect cash and cash equivalents (472) 71
Cash and cash equivalents at beginning of the period 149,408 118,925
Cash and cash equivalents at the end of the period € 132,414 € 85,713
v3.25.1
General Information
3 Months Ended
Mar. 31, 2025
General Information  
General Information

1. General Information

ProQR Therapeutics N.V., or “ProQR” or the “Company”, is a biotechnology company domiciled in the Netherlands that primarily focuses on the discovery and development of novel therapeutic medicines.

Since September 18, 2014, the Company’s ordinary shares have been listed on Nasdaq. They are currently trading at Nasdaq Capital Market under ticker symbol PRQR.

The Company was incorporated in the Netherlands, on February 21, 2012 (Chamber of Commerce no. 54600790) and was reorganized from a private company with limited liability to a public company with limited liability on September 23, 2014. The Company has its statutory seat in Leiden, the Netherlands. The address of its headquarters and registered office is Zernikedreef 9, 2333 CK Leiden, the Netherlands.

ProQR Therapeutics N.V. is the ultimate parent company of the following entities:

ProQR Therapeutics Holding B.V. (100%);
ProQR Therapeutics I B.V. (100%);
ProQR Therapeutics II B.V. (100%);
ProQR Therapeutics III B.V. (100%);
ProQR Therapeutics IV B.V. (100%);
ProQR Therapeutics V B.V. (100%);
ProQR Therapeutics VI B.V. (100%);
ProQR Therapeutics VII B.V. (100%);
ProQR Therapeutics VIII B.V. (100%);
ProQR Therapeutics IX B.V. (100%);
ProQR Therapeutics I Inc. (100%)

ProQR Therapeutics N.V. is also statutory director of Stichting Bewaarneming Aandelen ProQR (“ESOP Foundation”) and has full control over this entity.

As used in these condensed consolidated financial statements, unless the context indicates otherwise, all references to “ProQR” or the “Company” refer to ProQR Therapeutics N.V. including its subsidiaries and the ESOP Foundation.

v3.25.1
Significant Accounting Policies
3 Months Ended
Mar. 31, 2025
Significant Accounting Policies  
Significant Accounting Policies

2. Significant Accounting Policies

These interim condensed consolidated financial statements for the three month period ended March 31, 2025 have been prepared in accordance with IAS 34 Interim Financial Statements. They should be read in conjunction with the Company’s annual financial statements for the year ended December 31, 2024. These interim condensed consolidated financial statements do not include all information required for a complete set of financial statements prepared in accordance with IFRS Standards. However, selected explanatory notes are included to explain events and transactions that are significant to an understanding of the changes in the Company’s financial position and performance since the last annual financial statements. In the opinion of management, all events and transactions that are significant to an understanding of the changes in financial position and performance of the Company since the end of the last annual reporting period are disclosed in these interim condensed consolidated financial statements. The accounting policies adopted in the preparation of the interim condensed consolidated financial statements are consistent with those applied in the preparation of the Company’s annual financial statements for the year ended December 31, 2024.

During the quarter ended March 31, 2024, the Company invested in financial assets in the form of deposits with an original maturity of longer than three months but shorter than twelve months which are measured at amortized cost as they give rise on specified dates to cash flows that are solely payments of principal and interest on the principal amount outstanding.

The Company’s financial results have varied substantially, and are expected to continue to vary, from period to period. The Company believes that its ordinary activities are not linked to any particular seasonal factors.

The management of ProQR has, upon preparing and finalizing these interim condensed consolidated financial statements, assessed the Company’s ability to fund its operations for a period of at least one year after the date of signing these interim condensed consolidated financial statements. Management expects the Company to continue as a going concern based on its existing funding, taking into account the Company’s current cash position and the projected cash flows based on the activities under execution on the basis of ProQR’s business plan and budget. Thus, we continue to adopt the going concern basis of accounting in preparing the interim condensed consolidated financial statements.

The carrying amount of all financial assets and financial liabilities is a reasonable approximation of the fair value and therefore, information about the fair values of each class has not been disclosed.

The Company operates in one reportable segment, which comprises the discovery and development of innovative, RNA based therapeutics.

v3.25.1
Adoption of new and revised International Financial Reporting Standards
3 Months Ended
Mar. 31, 2025
Adoption of new and revised International Financial Reporting Standards  
Adoption of new and revised International Financial Reporting Standards

3. Adoption of New and Revised International Financial Reporting Standards

New Standards and Interpretations, which became effective as of January 1, 2025, did not have a material impact on our condensed consolidated financial statements.

v3.25.1
Critical Accounting Estimates and Judgments
3 Months Ended
Mar. 31, 2025
Critical Accounting Estimates and Judgments  
Critical Accounting Estimates and Judgments

4. Critical Accounting Estimates and Judgements

In the application of the Company’s accounting policies, management is required to make judgments, estimates and assumptions about the carrying amounts of assets and liabilities that are not readily apparent from other sources. The estimates and associated assumptions are based on historical experience and other factors that are considered to be relevant. Actual results may differ from these estimates.

The estimates and underlying assumptions are reviewed on an ongoing basis. Revisions to accounting estimates are recognized in the period in which the estimate is revised if the revision affects only that period or in the period of the revision and future periods if the revision affects both current and future periods.

The significant judgements made by management in applying the Company’s accounting policies and the key sources of estimation uncertainty were the same as those described in the Company’s annual financial statements for the year ended December 31, 2024.

(i) Revenue recognition for the Eli Lilly and Company research and collaboration agreement

a. Identification of the performance obligations

As further described in Note 13 the identification of the performance obligations for the Company’s original research and collaboration agreement with Eli Lilly and Company (“Lilly”), and the amended and restated research and collaboration agreement (collectively, the “Collaboration agreement”) involves significant judgement.

A key judgement was made in determining that the license granted to Lilly is not distinct from the associated research and development (“R&D”) services, due to the lack of stand-alone value of the license without the Company’s involvement and the significant interdependencies between the license and the R&D services to be provided by the Company. As a result, the license and the R&D services are accounted for together as a single combined performance obligation consisting of multiple activities that are not distinct.

b. Determining the timing of satisfaction of performance obligations

As further described in Note 13, before the handover of a compound to Lilly, the Company recognizes revenue over time, using an input method that estimates the satisfaction of the performance obligation as the percentage of labor hours incurred compared to the total estimated labor hours required to complete the promised services. As the Company’s estimate of the total labor hours required is dependent on the evolution of the research and development activities, it may be subject to change. If the progression and/or outcome of certain research and development activities would be different from the assumptions that were made during the preparation of these financial statements, this could lead to material adjustments to the total estimated labor hours, which might result in a reallocation of revenue between current and future periods. Our total deferred revenue balance related to this Lilly performance obligation amounts to € 47,329,000 at March 31, 2025 (December 31, 2024: € 50,930,000).

c. Determining the transaction price

The Company applied judgement to determine whether the equity investments made by Lilly in ProQR are part of the transaction price for the Collaboration agreement. The Company concluded that the differences between the prices that Lilly paid for the shares and the ProQR stock closing prices on the days of entering into the equity investment agreements arose because of the Company’s existing obligations to deliver research and development services to Lilly under the terms of the Collaboration agreement. Therefore, the above differences between the closing share prices on the agreement effective dates and the equity investment prices paid by Lilly are considered to be part of the transaction price of the contract and are initially allocated to deferred revenue.

The contract also includes variable consideration, but no variable consideration was included in the initial transaction price at the inception, as it is not highly probable that a significant reversal in the amount of cumulative revenue recognized will not occur. The Company includes such variable consideration in the transaction price when the uncertainty associated with the variable consideration is resolved.

The Collaboration agreement includes variable consideration in the form of development milestones, commercial milestones, and sales-based royalties based on the level of sales. As further described in Note 13, during March 31, 2025 the Company achieved development milestones during the ProQR research program under the agreement, which were added to the transaction price and recognized partially as revenue during 2025 based on the status of completion (satisfied part) of the single combined performance obligation.

(ii) Research and development expenditures

Research expenditures are reflected in the income statement. Development expenses are currently also reflected in the income statement because the criteria for capitalization are not met. At each balance sheet date, the Company estimates the level of service performed by the vendors and the associated costs incurred for the services performed.

Although we do not expect the estimates to be materially different from amounts actually incurred, the understanding of the status and timing of services performed relative to the actual status and timing of services performed may vary and could result in reporting amounts that are too high or too low in any particular period.

v3.25.1
Cash and Cash Equivalents
3 Months Ended
Mar. 31, 2025
Cash and Cash Equivalents.  
Cash and Cash Equivalents

5. Cash and Cash Equivalents

At March 31, 2025, the Company’s cash and cash equivalents were € 132,414,000 compared to € 149,408,000 at December 31, 2024. The cash balances are held at banks with investment grade credit ratings. Short-term credit ratings must be rated A-1/P-1/F1 at a minimum by at least one of the Nationally Recognized Statistical Rating Organizations (“NRSROs”) specifically Moody’s, Standard & Poor’s or Fitch. The cash at banks is at full disposal of the Company. Included in cash and cash equivalents are deposits fixed for at most 3-month periods at a time.

v3.25.1
Prepayments and Other Receivables
3 Months Ended
Mar. 31, 2025
Prepayments and Other Receivables.  
Prepayments and Other Receivables

6. Prepayments and Other Receivables

March 31, 

December 31, 

2025

2024

€1,000

€1,000

Prepayments

2,910

2,410

Other receivables

1,725

835

Accrued income from Rett Syndrome Research Trust

502

502

5,137

3,747

All receivables are considered short-term and due within one year. At March 31, 2025 and December 31, 2024 prepayments consisted principally of payments made by the Company for services not yet provided by vendors. At March 31, 2025 and December 31, 2024 other receivables consisted principally of accrued grant income and deposits. As at March 31, 2025 and December 31, 2024 the accrued grant income relating to Rett Syndrome Research Trust (“RSRT”) includes the initial fair value of the warrants issued to RSRT that was accounted for as a reduction of the transaction price. The RSRT agreement is described in Note 14. Other Income.

v3.25.1
Property, Plant and Equipment
3 Months Ended
Mar. 31, 2025
Property, Plant and Equipment.  
Property, Plant and Equipment

7. Property, Plant and Equipment

At March 31, 2025 and December 31, 2024, property plant and equipment consisted of buildings and leasehold improvements, laboratory equipment and other assets. Buildings and leasehold improvements include a right-of-use asset relating to the lease of our Leiden office and laboratory space, with a carrying amount of € 11,122,000 at March 31, 2025 (December 31, 2024: € 11,433,000).

v3.25.1
Other Current Liabilities
3 Months Ended
Mar. 31, 2025
Other current liabilities [Abstract]  
Other current liabilities

8. Other Current Liabilities

At March 31, 2025, other current liabilities amount to € 7,271,000 (December 31, 2024: € 8,849,000). At March 31, 2025 and December 31, 2024, other current liabilities consisted principally of accruals for services provided by vendors not yet billed, payroll related accruals and other miscellaneous liabilities.

v3.25.1
Borrowings
3 Months Ended
Mar. 31, 2025
Borrowings  
Borrowings

9. Borrowings

March 31, 

December 31, 

    

2025

2024

€1,000

€1,000

Innovation credit

2,899

2,899

Accrued interest on innovation credit

1,756

1,683

Total borrowings

4,655

4,582

Current portion

4,655

4,582

Total non-current borrowings

In December 2018, ProQR was awarded an Innovation credit for the sepofarsen program. Amounts were drawn under this facility from 2018 through 2022. The credit of € 3,907,000 was used to conduct the Phase 2/3 clinical study and efforts to obtain regulatory and ethical market approval (New Drug Applications (“NDA”)/ Marketing Authorization Applications (“MAA”)) of sepofarsen for LCA10. In the fourth quarter of 2023, ProQR made a partial repayment of the principal, amounting to € 1,008,000. The remaining amount payable of € 2,899,000 is recognized under current borrowings as at March 31, 2025 and December 31, 2024.

In December 2023, ProQR received a waiver for the remaining balance of the Innovation credit including accrued interest. As a result, the repayment of the total loan of € 4,292,000, including accrued interest, could be waived if conditions are met, subject to annual review. In January 2025, the waiver for the total balance of € 4,582,000, including interest, was again extended until December 31, 2025.

In September 2022, ProQR extinguished its debt with Pontifax and Kreos by repaying all outstanding principal amounts. Pontifax’ and Kreos’ warrants remain in place until their five-year economic life expires in 2025 and 2026. These warrants are accounted for as embedded derivatives and were recognized separately from the host contract as derivative financial liabilities at fair value through profit or loss.

v3.25.1
Lease Liabilities
3 Months Ended
Mar. 31, 2025
Lease Liabilities  
Lease Liabilities

10. Lease Liabilities

At March 31, 2025 and December 31, 2024, lease liabilities primarily consisted of the Company’s lease of office and laboratory facilities at Zernikedreef in Leiden, the Netherlands.

The Company leases office and laboratory facilities of 4,818 square meters at Zernikedreef in Leiden, the Netherlands, where our headquarters and our laboratories are located. The current lease agreement for these facilities terminates on June 30, 2031. The lease agreement contains no significant dismantling requirements.

The initial 10-year lease agreement for the Leiden office and laboratory facilities was accounted for as of commencement date July 1, 2020. This 10-year period was extended by 1 year to an 11-year period in December 2020. The lease contract may be extended for subsequent 5-year periods. As the Company is not reasonably certain to exercise these extension options, these are not included in the lease term.

The carrying amount of the right-of-use asset is disclosed in Note 7.

v3.25.1
Deferred Income
3 Months Ended
Mar. 31, 2025
Deferred Income  
Deferred Income

11. Deferred Income

The following table summarizes details of deferred income at March 31, 2025 and December 31, 2024. The nature of the deferred income is described in Note 13 and 14.

March 31, 

December 31, 

2025

2024

€1,000

€1,000

Payments from Eli Lilly and Company

19,030

21,501

Payments from Rett Syndrome Research Trust

220

441

Current deferred income

19,250

21,942

Payments from Eli Lilly and Company

28,299

29,429

Non-current deferred income

28,299

29,429

Total deferred income

47,549

51,371

c

v3.25.1
Shareholders' Equity
3 Months Ended
Mar. 31, 2025
Shareholders Equity  
Shareholders Equity

12. Shareholders’ Equity

The authorized share capital of the Company amounting to € 13,600,000 consists of 170,000,000 ordinary shares and 170,000,000 preference shares with a par value of € 0.04 per share. At March 31, 2025, 107,710,916 ordinary shares were issued. 105,342,963 ordinary shares were fully paid and 2,367,953 ordinary shares were held by the Company as treasury shares (December 31, 2024: 2,498,389).

In September 2024, the Company filed a shelf registration statement on Form F-3, which permitted: (a) the offering, issuance and sale by the Company of up to a maximum aggregate offering price of $ 300,000,000 of its ordinary shares, warrants and/or units; and (b) as part of the $ 300,000,000, the offering, issuance and sale by the Company of up to a maximum aggregate offering price of $ 75,000,000 of its ordinary shares that may be issued and sold under a sales agreement (the “sales agreement”) with Cantor Fitzgerald & Co. (“Cantor”) in one or more at-the-market (“ATM”) offerings. The Company will pay Cantor a commission equal to 3% of the gross proceeds of the sales price of all ordinary shares sold through it as sales agent under the sale agreement. As of December 31, 2024, no shares have been issued pursuant to this ATM facility.

In October 2024, the Company consummated an underwritten public offering of 18,000,000 ordinary shares (the “offering”) at a public offering price of $ 3.50 per share (the “public offering price”). In addition, the Company granted the underwriters a 30-day option to purchase up to 2,700,000 additional ordinary shares at the public offering price, less underwriting discounts and commissions. The option was partially exercised on October 31, 2024, resulting in the issuance of 1,940,072 shares. The gross proceeds from the Offering and subsequent partial exercise of the underwriters’ option, amounted to $ 69,790,000 (€ 64,600,000) while the transaction costs amounted to approximately € 4,365,000, resulting in net proceeds of approximately € 60,235,000.

Concurrently with the Offering, the Company entered into a share purchase agreement with Lilly in a separately negotiated transaction (the “concurrent private placement”), pursuant to which the Company agreed to offer and sell, and Lilly agreed to purchase, 3,523,538 ordinary shares at a price per share equal to the public offering price, for total gross proceeds of approximately $ 12,300,000, subject to a purchase price cap of $ 15,000,000, the consummation of the Offering and the satisfaction of other customary closing conditions. The proceeds of $ 12,300,000 million (€ 11,400,000) from the concurrent private placement were received on October 25, 2024. The ordinary shares purchased in the concurrent private placement are not subject to any underwriting discounts or commissions.

Translation reserve

The translation reserve comprises all foreign currency differences arising from the translation of the financial statements of foreign operations.

Share options

The Company operates an equity-settled share-based compensation plan, which was introduced in 2013. Options and Restricted Stock Units (“RSUs”) may be granted to employees, members of the Board and consultants. The compensation expenses included in operating costs for this plan in the three month period ended March 31, 2025 were € 758,000 (three month period ended March 31, 2024: € 736,000), of which € 566,000 was recorded in general and administrative costs (three month period ended March 31, 2024: € 577,000) and € 192,000 was recorded in research and development costs (three month period ended March 31, 2024: € 159,000).

v3.25.1
Revenue
3 Months Ended
Mar. 31, 2025
Revenue.  
Revenue

13. Revenue

Eli Lilly and Company collaboration

In September 2021, the Company entered into a global licensing and research collaboration with Lilly focused on the discovery, development, and commercialization of potential new medicines for genetic disorders in the liver and nervous system. ProQR and Lilly will use ProQR’s proprietary Axiomer® RNA editing platform to progress new drug targets toward clinical development and commercialization.

Under the terms of the agreement, ProQR received an upfront payment and equity consideration, and is eligible to receive milestone payments and royalties on the net sales of any resulting products. In September 2021, the Company issued 3,989,976 shares to Lilly, resulting in gross proceeds of $ 30,000,000 (€ 25,270,000). These shares were issued at a premium of $ 2,429,000 (€ 2,047,000), which was determined to be part of the transaction price and as such was initially recognized as deferred revenue. An up-front payment of $ 20,000,000 (€ 16,849,000) was received in October 2021.

In December 2022, the Company and Lilly amended their research and collaboration agreement described above, which expanded the collaboration. Under the amended and restated research and collaboration agreement, Lilly will gain access to additional targets in the central nervous system (“CNS”) and peripheral nervous system (“PNS”) with ProQR’s Axiomer platform.

As described under Note 12, pursuant to the amended and restated agreement, the Company issued 9,381,586 shares to Lilly in December 2022, resulting in gross proceeds of $ 15,000,000 (€ 14,122,000). These shares were issued at a discount of $ 480,000 (€ 451,000), which is accounted for as a reduction of the transaction price. In February 2023, ProQR also received an upfront payment of $ 60,000,000 (€ 56,412,000). Lilly has the ability to exercise an option to further expand the partnership for a consideration of $ 50,000,000.

With regard to the original and amended and restated research and collaboration agreements with Lilly, the Company concluded as follows:

The amended and restated research and collaboration agreement is accounted for as a separate contract under IFRS 15 given the group of promises to be delivered are distinct and are priced commensurate with stand-alone selling prices.
For each of the agreements, the company identified one performance obligation under IFRS 15, for the transfer of a license combined with the performance of research and development activities. The Company concluded that the license is not capable of being distinct and is not distinct in the context of the contract. ProQR’s services are evaluated as predominant at inception of the contract and the compounds resulting from the collaboration do not represent a series of distinct promises because they were not predetermined at the inception of the contract and can be terminated or replaced at the discretion of Lilly subject to the terms and conditions of the Collaboration agreement.
The transaction price of the agreement includes fixed components, consisting of an up-front fee and an equity component (premium or discount). The agreement also contains variable parts, notably milestones, which are included in the transaction price to the extent that it is highly probable that a significant reversal in the amount of cumulative revenue recognized will not occur when the uncertainty associated with the variable consideration is subsequently resolved. Development milestone payments to be reached during the ProQR research program will only be included to the extent that it is highly probable that a significant reversal in the amount of cumulative revenue recognized will not occur when the uncertainty associated with the milestones is subsequently resolved. Sales-based milestones and sales-based royalties will be included as the underlying sales occur.
Initially, the Company recognizes revenue over time, using an input method that estimates the satisfaction of the performance obligation as the percentage of labor hours incurred compared to the total estimated labor hours required to complete the promised services.

After the handover of a compound to Lilly:

The variable consideration for development milestones to be reached during the Lilly R&D activities is linked to a separable right to use the license which comes into existence for each successful compound transferred to Lilly. This license is a separate performance obligation and revenue will be recognized at a point in time when the development milestone for a license is achieved and the variable constraint is resolved.
The variable consideration for commercial milestones is linked to a separable right to use the license which comes into existence for each successful compound transferred to Lilly. This license is a separate performance obligation and will be recognized at a point in time when the commercial milestone for a license is achieved and the variable constraint is resolved.
For sales-based royalties, the license is the predominant item to which the royalty relates. The sales-based royalties will be recognized after the handover of the compound to Lilly (after completion of the initial performance obligation) and once the respective sale level occurs.  

During the three month period ended March 31, 2025, the Company reached milestones amounting to $ 1,000,000 (€ 918,000) under the agreement, which was added to the transaction price and recognized partially as revenue during the three month period ended March 31, 2025.

v3.25.1
Other income
3 Months Ended
Mar. 31, 2025
Other income  
Other income

14. Other Income

Three month period

ended March 31, 

    

2025

2024

€1,000

€1,000

Grant income

222

210

222

210

In January, 2024, the Company entered into an agreement with the RSRT that focuses on the design and development of editing oligonucleotides (“EONs”) using the Company’s Axiomer technology platform targeting the transcription factor Methyl CpG binding protein 2 (“MECP2”) and correcting mutations of interest. Under the agreement, RSRT awarded the Company up to € 1,015,000 as a research grant for the initial phase of the project that was received during 2024, out of which € 575,000 was recognized as Other Income during 2024 and the remaining part recorded as Deferred Income. In December 2024, the Company expanded partnership with RSRT to include an additional $ 8,150,000 in funding from the RSRT to support the advancement of the selected candidates into clinical trials. As at March 31, 2025 no amounts have been received under this agreement and the work has not yet commenced.

Grants are recognized in other income in the same period in which the related R&D costs are recognized.

v3.25.1
Research and Development Costs
3 Months Ended
Mar. 31, 2025
Research and development costs [Abstract]  
Research and Development Costs

15. Research and Development Costs

Research and development costs amount to € 12,323,000 for the three month period ended March 31, 2025 (three month period ended March 31, 2024: € 9,283,000) and are comprised of allocated employee costs including share-based payments, the costs of materials and laboratory consumables, outsourced activities, license and intellectual property costs and other allocated costs. Research and development costs increased compared to the same period in the prior year, mainly due to the Company’s increased outsourced research and development activities and full time employee equivalents (“FTE”) in the three month period of 2025.

v3.25.1
General and administrative costs
3 Months Ended
Mar. 31, 2025
General and administrative costs  
General and administrative costs

16. General and Administrative Costs

General and administrative costs amount to € 3,234,000 for the three month period ended March 31, 2025 (three month period ended March 31, 2024: € 3,452,000).

v3.25.1
Investments in Financial Assets
3 Months Ended
Mar. 31, 2025
Investments in Financial Assets  
Investments in Financial Assets

17. Investments in Financial Assets

Investment in financial assets consist of the Company’s investment in Phoenicis Therapeutics Inc. (“Phoenicis”) and Yarrow Biotechnology Inc. (“Yarrow”).

ProQR holds a 3.9% interest in Phoenicis. As at March 31, 2025, the investment amounts to € nil (December 31, 2024: € nil). Phoenicis discontinued its operations during the quarter ended September 30, 2024.

ProQR holds a 5.1% interest in Yarrow. As at March 31, 2025, the fair value of the Yarrow financial asset amounted to € nil (December 31, 2024: € nil).

v3.25.1
Income Taxes
3 Months Ended
Mar. 31, 2025
Income Taxes  
Income Taxes

18. Income Taxes

The current income tax liability amounts to € nil at March 31, 2025 (December 31, 2024: € nil). No significant temporary differences exist between accounting and tax results. Realization of deferred tax assets is dependent on future earnings, if any, the timing and amount of which are uncertain. Accordingly, the Company has not yet recognized any deferred tax asset related to operating losses.

Tax losses may be carried forward indefinitely. However, the offset of losses will be limited in a given year against the first € 1 million of taxable profit. For taxable profit in excess of this amount, losses may only be offset up to 50% of this excess. In addition, unused non-deductible interest expenses may be carried forward indefinitely. However, the offset will be limited in a given year against the higher of 20% of adjusted taxable profit or € 1.0 million of interest income.

v3.25.1
Related-Party Transactions
3 Months Ended
Mar. 31, 2025
Related-Party Transactions  
Related-Party Transactions

19. Related-Party Transactions

The Company does not have any transactions with related parties other than compensation to its Board members.

v3.25.1
Events After Balance Sheet Date
3 Months Ended
Mar. 31, 2025
Events After Balance Sheet Date  
Events After Balance Sheet Date

20. Events After Balance Sheet Date

None.

v3.25.1
Significant Accounting Policies (Policies)
3 Months Ended
Mar. 31, 2025
Significant Accounting Policies  
Revenue

(i) Revenue recognition for the Eli Lilly and Company research and collaboration agreement

a. Identification of the performance obligations

As further described in Note 13 the identification of the performance obligations for the Company’s original research and collaboration agreement with Eli Lilly and Company (“Lilly”), and the amended and restated research and collaboration agreement (collectively, the “Collaboration agreement”) involves significant judgement.

A key judgement was made in determining that the license granted to Lilly is not distinct from the associated research and development (“R&D”) services, due to the lack of stand-alone value of the license without the Company’s involvement and the significant interdependencies between the license and the R&D services to be provided by the Company. As a result, the license and the R&D services are accounted for together as a single combined performance obligation consisting of multiple activities that are not distinct.

b. Determining the timing of satisfaction of performance obligations

As further described in Note 13, before the handover of a compound to Lilly, the Company recognizes revenue over time, using an input method that estimates the satisfaction of the performance obligation as the percentage of labor hours incurred compared to the total estimated labor hours required to complete the promised services. As the Company’s estimate of the total labor hours required is dependent on the evolution of the research and development activities, it may be subject to change. If the progression and/or outcome of certain research and development activities would be different from the assumptions that were made during the preparation of these financial statements, this could lead to material adjustments to the total estimated labor hours, which might result in a reallocation of revenue between current and future periods. Our total deferred revenue balance related to this Lilly performance obligation amounts to € 47,329,000 at March 31, 2025 (December 31, 2024: € 50,930,000).

c. Determining the transaction price

The Company applied judgement to determine whether the equity investments made by Lilly in ProQR are part of the transaction price for the Collaboration agreement. The Company concluded that the differences between the prices that Lilly paid for the shares and the ProQR stock closing prices on the days of entering into the equity investment agreements arose because of the Company’s existing obligations to deliver research and development services to Lilly under the terms of the Collaboration agreement. Therefore, the above differences between the closing share prices on the agreement effective dates and the equity investment prices paid by Lilly are considered to be part of the transaction price of the contract and are initially allocated to deferred revenue.

The contract also includes variable consideration, but no variable consideration was included in the initial transaction price at the inception, as it is not highly probable that a significant reversal in the amount of cumulative revenue recognized will not occur. The Company includes such variable consideration in the transaction price when the uncertainty associated with the variable consideration is resolved.

The Collaboration agreement includes variable consideration in the form of development milestones, commercial milestones, and sales-based royalties based on the level of sales. As further described in Note 13, during March 31, 2025 the Company achieved development milestones during the ProQR research program under the agreement, which were added to the transaction price and recognized partially as revenue during 2025 based on the status of completion (satisfied part) of the single combined performance obligation.

Research and development expenditures

(ii) Research and development expenditures

Research expenditures are reflected in the income statement. Development expenses are currently also reflected in the income statement because the criteria for capitalization are not met. At each balance sheet date, the Company estimates the level of service performed by the vendors and the associated costs incurred for the services performed.

Although we do not expect the estimates to be materially different from amounts actually incurred, the understanding of the status and timing of services performed relative to the actual status and timing of services performed may vary and could result in reporting amounts that are too high or too low in any particular period.

v3.25.1
Prepayments and Other Receivables (Tables)
3 Months Ended
Mar. 31, 2025
Prepayments and Other Receivables.  
Prepayments and Other Receivables

March 31, 

December 31, 

2025

2024

€1,000

€1,000

Prepayments

2,910

2,410

Other receivables

1,725

835

Accrued income from Rett Syndrome Research Trust

502

502

5,137

3,747

v3.25.1
Borrowings (Tables)
3 Months Ended
Mar. 31, 2025
Borrowings  
Schedule of borrowings

March 31, 

December 31, 

    

2025

2024

€1,000

€1,000

Innovation credit

2,899

2,899

Accrued interest on innovation credit

1,756

1,683

Total borrowings

4,655

4,582

Current portion

4,655

4,582

Total non-current borrowings

v3.25.1
Deferred Income (Tables)
3 Months Ended
Mar. 31, 2025
Deferred Income  
Summary of deferred income

March 31, 

December 31, 

2025

2024

€1,000

€1,000

Payments from Eli Lilly and Company

19,030

21,501

Payments from Rett Syndrome Research Trust

220

441

Current deferred income

19,250

21,942

Payments from Eli Lilly and Company

28,299

29,429

Non-current deferred income

28,299

29,429

Total deferred income

47,549

51,371

v3.25.1
Other income (Tables)
3 Months Ended
Mar. 31, 2025
Other income  
Schedule of other income

Three month period

ended March 31, 

    

2025

2024

€1,000

€1,000

Grant income

222

210

222

210

v3.25.1
General Information (Details)
3 Months Ended
Mar. 31, 2025
ProQR Therapeutics Holding B.V. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
ProQR Therapeutics I B.V. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
ProQR Therapeutics II B.V. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
ProQR Therapeutics III B.V. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
ProQR Therapeutics IV B.V. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
ProQR Therapeutics V B.V. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
ProQR Therapeutics VI B.V. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
ProQR Therapeutics VII B.V. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
ProQR Therapeutics VIII B.V. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
ProQR Therapeutics IX B.V. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
ProQR Therapeutics I Inc. [Member]  
Disclosure of subsidiaries [line items]  
Proportion of ownership interest in subsidiary 100.00%
v3.25.1
General Information - Revision of comparative figures (Details) - EUR (€)
€ in Thousands
3 Months Ended
Mar. 31, 2025
Mar. 31, 2024
Dec. 31, 2024
Dec. 31, 2023
Equity attributable to owners of the Company € 78,935   € 88,560  
Deferred income 47,549   51,371  
Revenue 4,519 € 4,450    
Result for the year (10,079) (7,658)    
Equity 78,935 34,821 88,560 € 41,390
Changes in working capital 6,721 9,224    
Accumulated Deficit        
Result for the year (10,079) (7,658)    
Equity € (436,231) € (408,190) € (427,158) € (400,850)
v3.25.1
Significant Accounting Policies (Details)
3 Months Ended
Mar. 31, 2025
segment
Significant Accounting Policies  
Number of reportable segment 1
v3.25.1
Critical Accounting Estimates and Judgements (Details)
€ in Thousands, $ in Thousands
Mar. 31, 2025
EUR (€)
Dec. 31, 2024
EUR (€)
Sep. 30, 2021
EUR (€)
Sep. 30, 2021
USD ($)
Disclosure of disaggregation of revenue from contracts with customers [line items]        
Deferred income € 47,549 € 51,371    
Eli Lilly and Company        
Disclosure of disaggregation of revenue from contracts with customers [line items]        
Deferred income € 47,329 € 50,930 € 2,047 $ 2,429
v3.25.1
Cash and Cash Equivalents (Details) - EUR (€)
€ in Thousands
Mar. 31, 2025
Dec. 31, 2024
Mar. 31, 2024
Dec. 31, 2023
Cash and Cash Equivalents.        
Cash and cash equivalents € 132,414 € 149,408 € 85,713 € 118,925
v3.25.1
Prepayments and Other Receivables (Details) - EUR (€)
€ in Thousands
Mar. 31, 2025
Dec. 31, 2024
Prepayments and Other Receivables.    
Prepayments € 2,910 € 2,410
Other receivables 1,725 835
Accrued income from Rett Syndrome Research Trust 502 502
Total Prepayments and Other Receivables € 5,137 € 3,747
v3.25.1
Property, Plant and Equipment (Details) - EUR (€)
€ in Thousands
Mar. 31, 2025
Dec. 31, 2024
Office and laboratory facilities at Zernikedreef in Leiden, the Netherlands    
Property, Plant and Equipment    
Right-of-use assets € 11,122 € 11,433
v3.25.1
Other Current Liabilties (Details) - EUR (€)
€ in Thousands
Mar. 31, 2025
Dec. 31, 2024
Other current liabilities [Abstract]    
Other current liabilities € 7,271 € 8,849
v3.25.1
Borrowings (Details) - EUR (€)
€ in Thousands
1 Months Ended 3 Months Ended
Sep. 30, 2022
Dec. 31, 2023
Mar. 31, 2025
Jan. 31, 2025
Dec. 31, 2024
Oct. 12, 2018
Disclosure of detailed information about borrowings [line items]            
Total borrowings     € 4,655   € 4,582  
Current portion     4,655   4,582  
Pontifax and Kreos warrants            
Disclosure of detailed information about borrowings [line items]            
Warrants, economic lifetime 5 years          
Innovation credit            
Disclosure of detailed information about borrowings [line items]            
Borrowings excluding accrued interest     2,899   2,899  
Accrued interest     1,756   € 1,683  
Current borrowings excluding accrued interest     € 2,899      
Notional amount           € 3,907
Repayment of borrowings   € 1,008        
Total conditional waiver of debt   € 4,292   € 4,582    
v3.25.1
Lease Liabilities (Details) - Office and laboratory facilities at Zernikedreef in Leiden, the Netherlands
€ in Thousands
1 Months Ended 3 Months Ended
Jul. 01, 2020
Dec. 31, 2020
Mar. 31, 2025
EUR (€)
Dec. 31, 2024
EUR (€)
Disclosure of quantitative information about right-of-use assets [line items]        
Area under lease | m²     4,818  
Lease term 10 years 11 years    
Lease extension term   1 year    
Lease, current extension period under option     5 years  
Right-of-use asset | €     € 11,122 € 11,433
v3.25.1
Deferred income (Details)
€ in Thousands, $ in Thousands
Mar. 31, 2025
EUR (€)
Dec. 31, 2024
EUR (€)
Sep. 30, 2021
EUR (€)
Sep. 30, 2021
USD ($)
Disclosure of disaggregation of revenue from contracts with customers [line items]        
Current deferred income € 19,250 € 21,942    
Non-current deferred income including non-current contract liabilities 28,299 29,429    
Total deferred income 47,549 51,371    
Eli Lilly and Company        
Disclosure of disaggregation of revenue from contracts with customers [line items]        
Current deferred income 19,030 21,501    
Non-current deferred income including non-current contract liabilities 28,299 29,429    
Total deferred income 47,329 50,930 € 2,047 $ 2,429
Rett Syndrome Research Trust        
Disclosure of disaggregation of revenue from contracts with customers [line items]        
Current deferred income € 220 € 441    
v3.25.1
Shareholders' Equity - Share capital (Details) - EUR (€)
1 Months Ended
Dec. 31, 2022
Sep. 30, 2021
Mar. 31, 2025
Dec. 31, 2024
Shareholders Equity        
Authorized share capital     € 13,600,000  
Par value per share     € 0.04  
Eli Lilly and Company        
Shareholders Equity        
Issue of ordinary shares (in shares) 9,381,586 3,989,976    
Ordinary        
Shareholders Equity        
Number of shares issued     107,710,916  
Number of shares authorised     170,000,000  
Number of shares issued and fully paid     105,342,963  
Treasury shares     2,367,953 2,498,389
Preferred        
Shareholders Equity        
Number of shares authorised     170,000,000  
v3.25.1
Shareholders' Equity - Sale of shares (Details)
$ / shares in Units, € in Thousands
1 Months Ended 12 Months Ended
Oct. 31, 2024
shares
Oct. 25, 2024
USD ($)
shares
Oct. 25, 2024
EUR (€)
shares
Oct. 31, 2024
USD ($)
$ / shares
shares
Oct. 31, 2024
EUR (€)
shares
Dec. 31, 2024
shares
Sep. 30, 2024
USD ($)
2024 shelf registration statement              
Disclosure of classes of share capital [line items]              
Maximum offering price in shelf registration statement | $             $ 300,000,000
At the market offerings with Cantor Fitzgerald and Co under shelf registration statement              
Disclosure of classes of share capital [line items]              
Maximum offering price in shelf registration statement | $             $ 75,000,000
Percentage of commission payable for gross proceeds from sales agreement             3.00%
Issue of ordinary shares (in shares)           0  
October 2024 underwritten public offering              
Disclosure of classes of share capital [line items]              
Issue of ordinary shares (in shares)       18,000,000 18,000,000    
Price per share | $ / shares       $ 3.5      
Proceeds from issuing shares       $ 69,790,000 € 64,600    
Payments for share issue costs | €         4,365    
Net proceeds from issuing shares | €         € 60,235    
Underwriters' option in connection to October 2024 underwritten public offering              
Disclosure of classes of share capital [line items]              
Issue of ordinary shares (in shares) 1,940,072            
Duration of underwriters' option       30 days 30 days    
Number of shares callable for options issued 2,700,000     2,700,000 2,700,000    
Share purchase agreement with Eli Lilly and Company              
Disclosure of classes of share capital [line items]              
Issue of ordinary shares (in shares)   3,523,538 3,523,538        
Proceeds from issuing shares   $ 12,300,000 € 11,400        
Purchase price cap, share purchase agreement | $   $ 15,000,000          
v3.25.1
Shareholders' Equity - Share options (Details) - EUR (€)
€ in Thousands
3 Months Ended
Mar. 31, 2025
Mar. 31, 2024
Disclosure of terms and conditions of share-based payment arrangement [line items]    
Equity-settled share based payments € 758 € 736
IFRS General and administrative costs    
Disclosure of terms and conditions of share-based payment arrangement [line items]    
Equity-settled share based payments 566 577
Research and development costs    
Disclosure of terms and conditions of share-based payment arrangement [line items]    
Equity-settled share based payments € 192 € 159
v3.25.1
Revenue (Details)
€ in Thousands
1 Months Ended 3 Months Ended
Feb. 28, 2023
EUR (€)
Feb. 28, 2023
USD ($)
Dec. 31, 2022
EUR (€)
shares
Dec. 31, 2022
USD ($)
shares
Oct. 31, 2021
EUR (€)
Oct. 31, 2021
USD ($)
Sep. 30, 2021
EUR (€)
shares
Sep. 30, 2021
USD ($)
shares
Mar. 31, 2025
EUR (€)
Mar. 31, 2025
USD ($)
Mar. 31, 2025
USD ($)
Dec. 31, 2024
EUR (€)
Sep. 30, 2021
USD ($)
Disclosure of disaggregation of revenue from contracts with customers [line items]                          
Deferred income | €                 € 47,549     € 51,371  
Eli Lilly and Company                          
Disclosure of disaggregation of revenue from contracts with customers [line items]                          
Deferred income             € 2,047   € 47,329     € 50,930 $ 2,429,000
Issue of ordinary shares (in shares) | shares     9,381,586 9,381,586     3,989,976 3,989,976          
Proceeds from issuing shares     € 14,122 $ 15,000,000     € 25,270 $ 30,000,000          
Discount on shares issued     € 451 $ 480,000                  
Additional consideration to be received if counterparty exercises option to expand partnership | $                     $ 50,000,000    
Number of performance obligations in collaboration agreement                 1 1      
Milestone payments received         € 16,849 $ 20,000,000              
Value of milestones reached during the period                 € 918 $ 1,000,000      
Eli Lilly and Company | Milestone payments                          
Disclosure of disaggregation of revenue from contracts with customers [line items]                          
Milestone payments received € 56,412 $ 60,000,000                      
v3.25.1
Other income (Details) - EUR (€)
€ in Thousands
3 Months Ended
Mar. 31, 2025
Mar. 31, 2024
Other income    
Grant income € 222 € 210
Total other income € 222 € 210
v3.25.1
Other income - Narrative (Details)
€ in Thousands, $ in Thousands
3 Months Ended 12 Months Ended
Mar. 31, 2025
EUR (€)
Mar. 31, 2024
EUR (€)
Dec. 31, 2024
EUR (€)
Dec. 31, 2024
USD ($)
Jan. 31, 2024
EUR (€)
Other Income [Line Items]          
Grant income € 222 € 210      
Rett Syndrome Research Trust          
Other Income [Line Items]          
Grant income     € 575    
Maximum grant receivable for the initial phase of the project         € 1,015
Maximum grant receivable for additional phase of the project | $       $ 8,150  
Receipts € 0        
v3.25.1
Research and Development Costs (Details) - EUR (€)
€ in Thousands
3 Months Ended
Mar. 31, 2025
Mar. 31, 2024
Research and development costs [Abstract]    
Research and development costs € 12,323 € 9,283
v3.25.1
General and administrative costs (Details) - EUR (€)
€ in Thousands
3 Months Ended
Mar. 31, 2025
Mar. 31, 2024
General and administrative costs    
General and administrative expense € 3,234 € 3,452
v3.25.1
Investments in Financial Assets (Details) - EUR (€)
€ in Thousands
Mar. 31, 2025
Dec. 31, 2024
Phoenicis Therapeutics Inc.    
Disclosure of Investment in Financial Asset and Gain on Disposal of Associate [Line items]    
Proportion of ownership interest 3.90%  
Financial assets at fair value through other comprehensive income € 0 € 0
Yarrow Biotechnology, Inc    
Disclosure of Investment in Financial Asset and Gain on Disposal of Associate [Line items]    
Proportion of ownership interest 5.10%  
Financial assets at fair value through other comprehensive income € 0 € 0
v3.25.1
Income taxes (Details) - EUR (€)
€ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2025
Dec. 31, 2024
Income Taxes      
Current tax liabilities   € 0 € 0
Tax expense (income), continuing operations € 3    

ProQR Therapeutics NV (NASDAQ:PRQR)
Historical Stock Chart
From Jun 2025 to Jul 2025 Click Here for more ProQR Therapeutics NV Charts.
ProQR Therapeutics NV (NASDAQ:PRQR)
Historical Stock Chart
From Jul 2024 to Jul 2025 Click Here for more ProQR Therapeutics NV Charts.