InflaRx (Nasdaq: IFRX), a clinical-stage biopharmaceutical company developing anti-inflammatory therapeutics by targeting the complement system, announced today financial results for the three months ended March 31, 2021.

“We have made significant progress with our vilobelimab clinical programs in the first few months of 2021,” said Prof. Niels C. Riedemann, Chief Executive Officer and Founder of InflaRx. “The team has worked tirelessly to progress the enrollment of our severe COVID-19 trial and we now expect the interim analysis to occur in the third quarter of this year. Despite the increase in vaccinations, patients remain in urgent need of better treatments for severe COVID-19. For HS, following feedback on the Special Protocol Assessment, we plan to continue our discussions with the FDA about the design of our Phase III trial in a Type A meeting. Following the positive safety data from our US ANCA-associated vasculitis trial, we are looking forward to data readouts in our European AAV trial by the end of the year. In our Pyoderma Gangraenosum trial we have reached target enrollment and expect additional data readouts in 2021.”

Recent Highlights and R&D Update

Issuance of Common Shares and WarrantsOn February 25, 2021, the Company sold an aggregate of 15,000,000 common shares through a public offering. The common shares were sold at a price of $5.00 per share. For each common share purchased, an investor also received a warrant to purchase a common share at an exercise price of $5.80. The warrants are exercisable immediately and have a term of up to one year. The shares and warrants were issued and the transaction closed on March 1, 2021 with gross offering proceeds to the Group (not including any potential proceeds from the exercise of warrants) of $75.0 million (€62.2 million), before deducting $4.5 million (€3.7 million) in underwriting discounts and other offering expenses of $0.4 million (€0.3 million).

Vilobelimab for Hidradenitis Suppurativa (HS)In Q1, InflaRx submitted a Special Protocol Assessment (SPA) to the U.S. FDA for the Phase III HS program and in May the Company received an official response. The FDA agreed to the dosing regimen in the protocol but did not agree with the assessment of the primary endpoint using the International Hidradenitis Suppurativa Severity Score (IHS4). At the FDA’s suggestion, InflaRx plans to request a Type A meeting to discuss the primary endpoint measure in more detail.

In Europe, as previously reported in 2020, InflaRx received scientific advice from the European Medicines Agency (EMA) about the European pathway for regulatory approval, including supporting the use of the IHS4 score as the primary endpoint.

Once InflaRx receives final feedback from the FDA on the proposed Phase III primary endpoint, the Company will determine the best path forward for the global development program in HS.

Vilobelimab for Severe COVID-19The Phase III part of the global Phase II/III trial evaluating vilobelimab in mechanically ventilated patients with COVID-19 was initiated in mid-September 2020, and recruitment has reached 178 patients, with 38 sites initiated across several countries in Europe and Latin America. Once 180 patients are enrolled and reach the 28-day endpoint, a blinded interim analysis will be conducted by an independent Data Safety Monitoring Board (DSMB) to continue the trial or stop for efficacy or futility. The recommendation of the DSMB based on the interim analysis is anticipated in Q3 of this year. Additional sites in other countries are expected to be added, including in the US. Topline data for all 360 enrolled patients at the 28-day mortality primary endpoint from the trial are expected to be available by the end of 2021.

Vilobelimab for ANCA-associated Vasculitis (AAV)In the US IXPLORE clinical Phase II study of IFX-1 in AAV, all patients have completed treatment. In May 2021, InflaRx reported topline data for the study, indicating that vilobelimab, when given in addition to best standard of care proved to be safe and well tolerated. Furthermore, InflaRx previously reported that both Part 1 and Part 2 of the AAV Phase II study in Europe (IXCHANGE) are fully enrolled. Data from the randomized, double-blind, placebo-controlled trial with 57 patients are expected by the end of 2021.

Vilobelimab in Cutaneous Squamous Cell Carcinoma (cSCC) The Company has recently announced plans to initiate an open label, multicenter Phase II study evaluating vilobelimab alone and in combination with pembrolizumab in patients with PD-1 or PD-L1 inhibitor resistant/refractory locally advanced or metastatic cSCC.

The Phase II trial is expected to start enrolling patients in the second quarter of 2021 at sites in Europe, the US and other countries. The study will investigate two independent arms: vilobelimab alone and vilobelimab in combination with pembrolizumab. The main objectives of the trial are to assess antitumor activity and safety of vilobelimab monotherapy and to determine the maximum tolerated or recommended dose, safety and antitumor activity in the combination arm.

Vilobelimab in Pyoderma Gangraenosum The Phase IIa open label trial has reached the target enrollment goal of 18 patients with moderate to severe PG at sites in the US, Canada and Europe. Promising initial data from the first five patients in the study were announced in 2020. A second interim analysis, including six patients treated at the second dose group until day 99, are expected to be available by the end of 2021. Final results from all patients, including the highest dose group, are expected in 2022.

Financial highlights – Q1 2021

Research and development expenses incurred for the three months ended March 31, 2021 decreased over the corresponding period in 2020 by €2.4 million. This decline was primarily due to no contribution of expense in the period from the Phase IIb clinical development of vilobelimab in HS since this study was completed in 2020, with only limited residual activities thereafter. This was partly offset by the expenses in relation to the COVID-19 trial. These two factors led to €1.1 million of lower manufacturing costs which significantly contributed to an overall decline in third-party expenses of €2.6 million. The €0.4 million increase in personnel expenses was mainly related to equity-settled share-based compensation.

General and administrative expenses increased by €0.5 million to €3.0 million for the three months ended March 31, 2021, from €2.6 million for the three months ended March 31, 2020. This increase is attributable to higher expenses from equity-settled share-based compensation recognized in personnel expenses (€0.5 million). Additionally, legal, consulting and other expenses decreased by €0.1 million to €1.0 million for the three months ended March 31, 2021, from €1.1 million for the three months ended March 31, 2020.

Net financial result increased by €0.3 million to €1.8 million for the three months ended March 31, 2021, from €1.5 million for the three months ended March 31, 2020. This increase is mainly attributable to higher foreign exchange gains, which increased by €1.2 million and higher foreign exchange losses of €0.6 million while interest on marketable securities declined by €0.4 million. Other finance expenses for the three months ended March 31, 2021 include a €48 thousand gain from a reduction in the allowance for expected credit loss on marketable securities.

Net loss for the three months ended March 31, 2021 was €6.1 million, compared to €8.2 million for the three month ended March 31, 2020. On March 31, 2021, the Company’s total funds available were approximately €137.8 million, composed of cash and cash equivalents (€78.7 million) and financial assets (€59.1 million).

Net cash used in operating activities decreased to €10.4 million in the three months ended March 31, 2021, from €10.5 million in the three months ended March 31, 2020.

Additional information regarding these results and other relevant information is included in the notes to the unaudited Condensed Consolidated Financial Statements as of March 31, 2021, as well as the financial statements as of December 31, 2020 in “ITEM 18. Financial statements,” which is included in InflaRx’s Annual Report on Form 20-F as filed with the U.S. Securities and Exchange Commission (SEC).

InflaRx N.V. and subsidiariesUnaudited Condensed Consolidated Statements of Operations andComprehensive Loss for the three months ended March 31, 2021 and 2020

  For the three months endedMarch 31,
(in €, except for share data) 2021(unaudited)   2020(unaudited)
       
Operating Expenses      
Research and development expenses (4,906,885)   (7,298,799)
General and administrative expenses (3,022,339)   (2,564,803)
Total Operating Expenses (7,929,224)   (9,863,601)
Other income 5,462   94,960
Other expenses (565)   (5,720)
Operating Result (7,924,327)   (9,774,362)
Finance income 22,962   401,435
Finance expenses (3,684)   (2,147)
Foreign exchange result 1,731,671   1,141,677
Other financial result 48,000  
Income Taxes  
Loss for the Period (6,125,378)   (8,233,397)
       
Share Information      
Weighted average number of shares outstanding 33,807,774   26,105,255
Loss per share (basic/diluted) (0.18)   (0.32)
       
Loss for the Period (6,125,378)   (8,233,871)
Other comprehensive income (loss) that may be reclassified to profit or loss in subsequent periods:      
Exchange differences on translation of foreign currency 3,504,699   1,713,868
Total Comprehensive Loss (2,620,679)   (6,519,529)

InflaRx N.V. and subsidiariesUnaudited Condensed Consolidated Statements of Financial Positionas of March 31, 2021 and December 31, 2020

in € March 31,2021(unaudited)   December 31,2020
       
ASSETS      
Non-current assets      
Property and equipment 383,762   408,263
Right-of-use assets 457,513   546,694
Intangible assets 320,645   350,183
Other assets 358,767   353,522
Financial assets 272,443   272,268
Total non-current assets 1,793,130   1,930,930
Current assets      
Current other assets 6,527,973   3,734,700
Current tax assets 1,360,125   1,419,490
Financial assets 58,834,268   55,162,033
Cash and cash equivalents 78,734,662   25,968,681
Total current assets 145,457,028   86,284,904
TOTAL ASSETS 147,250,158   88,215,834
       
EQUITY AND LIABILITIES      
Equity      
Issued capital 5,302,354   3,387,410
Share premium 280,261,994   220,289,876
Other capital reserves 27,980,274   26,259,004
Accumulated deficit (174,470,998)   (168,345,620)
Other components of equity (222,091)   (3,726,791)
Total equity 138,851,532   77,863,880
Non-current liabilities      
Lease liabilities 137,586   220,525
Other liabilities 34,352   33,323
Total non-current liabilities 171,938   253,847
Current liabilities      
Trade and other payables 7,107,880   8,258,133
Lease liabilities 330,969   338,516
Employee benefits 429,621   1,368,731
Other financial liabilities 358,217   117,727
Provisions   15,000
Total current liabilities 8,226,687   10,098,107
Total Liabilities 8,398,626   10,351,954
TOTAL EQUITY AND LIABILITIES 147,250,158   88,215,834

InflaRx N.V. and subsidiariesUnaudited Condensed Consolidated Statements of Changes in Shareholders’Equity for the three months ended March 31, 2021 and 2020

(in €, except for share data) Issuedcapital   Sharepremium   Othercapitalreserves   Accumulateddeficit   Othercomponentof equity   Totalequity
                       
Balance as of January 1, 2021 3,387,410   220,289,876   26,259,004   (168,345,620)   (3,726,790)   77,863,880
Loss for the period       (6,125,378)     (6,125,378)
Exchange differences on translation of foreign currency         3,504,699   3,504,699
Total comprehensive loss       (6,125,378)   3,504,699   (2,620,679)
Issuance of common shares and warrants 1,873,203   63,269,346         65,142,549
Transaction costs   (4,219,222)         (4.219.222)
Equity-settled share-based payments     1,721,270       1,721,270
Share options exercised 41,741   921,994         963,735
Balance as of March 31, 2021 5,302,354   280,261,994   27,980,274   (174,470,998)   (222,091)   138,851,532
                       
Balance as of January 1, 2020 3,132,631   211,006,606   25,142,213   (134,362,006)   2,227,228   107,146,673
Loss for the period       (8,233,397)     (8,233,397)
Exchange differences on translation of foreign currency         1,713,868   1,713,868
Total comprehensive loss       (8,233,397)   1,713,868   (6,519,529)
Equity-settled share-based pay-ments     901,033       901,033
Balance as of March 31, 2020 3,132,631   211,006,606   26,043,246   (142,595,403)   3,941,097   101,528,177

InflaRx N.V. and subsidiariesUnaudited Condensed Consolidated Statements of Cash Flows for the three months ended March 31, 2021 and 2020

in € For the three months ended March 31, 2021(unaudited)   For the three months ended March 31, 2020(unaudited)
       
Operating activities      
Loss for the period (6,125,378)   (8,233,397)
Adjustments for:      
Depreciation & amortization of property and equipment, right-of-use assets and intangible assets 168,343   182,356
Net finance income (1,798,949)   (399,288)
Share-based payment expense 1,721,270   901,033
Net foreign exchange differences 193,847   (1,141,678)
Other non-cash adjustments   (129,122)
Changes in:      
Other assets (2,739,152)   188,476
Employee benefits (952,820)   (428,526)
Other liabilities 240,229   1,953
Trade and other payables (1,150,252)   (1,922,724)
Interest received 33,189   462,342
Interest paid (3,780)   (2,246)
Net cash used in operating activities (10,413,453)   (10,520,819)
Investing activities      
Purchase of intangible assets, property and equipment (17,062)   (27,686)
Purchase of current financial assets (14,985,026)   (23,412,469)
Proceeds from the maturity of financial assets 13,952,522   20,724,386
Net cash from/ (used in) investing activities (1,049,566)   (2,715,769)
Financing activities      
Proceeds from issuance of common shares 65,142,549  
Transaction costs from issuance of common shares (4,219,222)  
Proceeds from exercise of share options 963,735  
Repayment of lease liabilities (90,716)   (88,339)
Net cash from/ (used in) financing activities 61,796,346   (88,339)
Net increase/(decrease) in cash and cash equivalents 50,333,328   (13,324,927)
Effect of exchange rate changes on cash and cash equivalents 2,432,654   1,277,255
Cash and cash equivalents at beginning of period 25,968,681   33,131,280
Cash and cash equivalents at end of period 78,734,662   21,083,608

About vilobelimab (IFX-1):

Vilobelimab is a first-in-class monoclonal anti-human complement factor C5a antibody, which highly and effectively blocks the biological activity of C5a and demonstrates high selectivity towards its target in human blood. Thus, vilobelimab leaves the formation of the membrane attack complex (C5b-9) intact as an important defense mechanism, which is not the case for molecules blocking the cleavage of C5. Vilobelimab has been demonstrated to control the inflammatory response driven tissue and organ damage by specifically blocking C5a as a key “amplifier” of this response in pre-clinical studies. Vilobelimab is believed to be the first monoclonal anti-C5a antibody introduced into clinical development. Approximately 300 people have been treated with vilobelimab in clinical trials, and the antibody has been shown to be well tolerated. Vilobelimab is currently being developed for various indications, including Hidradenitis Suppurativa, ANCA-associated vasculitis, Pyoderma Gangraenosum and COVID-19 pneumonia.

About InflaRx N.V.:

InflaRx (Nasdaq: IFRX) is a clinical-stage biopharmaceutical company focused on applying its proprietary anti-C5a technology to discover and develop first-in-class, potent and specific inhibitors of C5a. Complement C5a is a powerful inflammatory mediator involved in the progression of a wide variety of autoimmune and other inflammatory diseases. InflaRx was founded in 2007, and the group has offices and subsidiaries in Jena and Munich, Germany, as well as Ann Arbor, MI, USA. For further information please visit www.inflarx.com.

Contacts:

InflaRx N.V.

Jordan Zwick – Chief Strategy OfficerEmail: IR@inflarx.deTel: +1 917-338-6523

MC Services AG

Katja Arnold, Laurie Doyle, Andreas JungferEmail: inflarx@mc-services.euEurope: +49 89-210 2280US: +1-339-832-0752

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 “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “intend,” “target,” “project,” “believe,” “estimate,” “predict,” “potential” or “continue” and similar expressions. Forward-looking statements appear in a number of places throughout this release and may include statements regarding our intentions, beliefs, projections, outlook, analyses and current expectations concerning, among other things, our ongoing and planned preclinical development and clinical trials; the impact of the COVID-19 pandemic on the Company; the timing and our ability to commence and conduct clinical trials; potential results from current or potential future collaborations; our ability to make regulatory filings, obtain positive guidance from regulators, and obtain and maintain regulatory approvals for our product candidates; our intellectual property position; our ability to develop commercial functions; expectations regarding clinical trial data; our results of operations, cash needs, financial condition, liquidity, prospects, future transactions, growth and strategies; the industry in which we operate; the trends that may affect the industry or us and the risks uncertainties and other factors described under the heading “Risk Factors” in InflaRx’s periodic filings with the Securities and Exchange Commission. These statements speak only as of the date of this press release and involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. 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.

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