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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
WASHINGTON,
D.C. 20549
FORM
8-K
CURRENT
REPORT
Pursuant
to Section 13 or 15(d) of the
Securities
Exchange Act of 1934
Date
of Report (Date of earliest event reported): August 10, 2023
PULMATRIX,
INC.
(Exact
name of registrant as specified in its charter)
Delaware |
|
001-36199 |
|
46-1821392 |
(State
or other jurisdiction
of
incorporation) |
|
(Commission
File Number) |
|
(IRS
Employer
Identification
No.) |
99
Hayden Avenue, Suite 390
Lexington,
MA 02421
(Address
of principal executive offices) (Zip Code)
(781)
357-2333
(Registrant’s
telephone number, including area code)
N/A
(Former
name or former address, if changed since last report)
Check
the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under
any of the following provisions:
☐ |
Written
communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
|
|
☐ |
Soliciting
material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
|
|
☐ |
Pre-commencement
communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
|
|
☐ |
Pre-commencement
communications pursuant to Rule 13e-4 (c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities
registered pursuant to Section 12(b) of the Act:
Title
of each class |
|
Trading
Symbol(s) |
|
Name
of exchange
on
which registered |
Common
Stock, par value $0.0001 per share |
|
PULM |
|
The
NASDAQ Stock Market LLC |
Indicate
by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405
of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging
growth company ☐
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Item
2.02 Results of Operations and Financial Condition.
On
August 10, 2023, Pulmatrix, Inc. issued a press release announcing its financial results for the second fiscal quarter ended June 30,
2023 and provided a corporate update. A copy of the press release is furnished as Exhibit 99.1 hereto and is incorporated herein by reference.
In
accordance with General Instruction B.2 of Form 8-K, the information in this Current Report on Form 8-K, including Exhibit 99.1, being
furnished pursuant to Item 2.02, shall not be deemed to be “filed” for the purposes of Section 18 of the Securities Exchange
Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, and shall not be incorporated
by reference into any registration statement or other document filed under the Securities Act of 1933, as amended, or the Exchange Act,
except as shall be expressly set forth by specific reference in such filing.
Item
9.01 Financial Statements and Exhibits.
(d)
Exhibits
*
This exhibit is furnished pursuant to Item 2.02 and shall not be deemed to be “filed.”
SIGNATURES
Pursuant
to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its
behalf by the undersigned hereunto duly authorized.
|
PULMATRIX,
INC. |
|
|
|
Date:
August 10, 2023 |
By: |
/s/
Teofilo Raad |
|
|
Teofilo
Raad |
|
|
Chief
Executive Officer |
Exhibit
99.1
Pulmatrix
Announces Second Quarter 2023 Financial Results and Provides Corporate Update
Subject
enrollment for the Phase 2b study of PUR1900 is ongoing with five additional sites added during Q2, totaling thirteen active sites to
date in four countries, and topline data anticipated in Q3 2024
Submitted
an IND for a Phase 2 study of PUR3100 for Acute Migraine
$25.8
million in cash and cash equivalents at the end of Q2 2023 providing projected cash runway into Q1 2025
Bedford,
Mass., August 10, 2023 – Pulmatrix, Inc. (NASDAQ: PULM), a clinical-stage biopharmaceutical company developing innovative inhaled
therapies to address serious pulmonary and central nervous system disease using its patented iSPERSE™ technology, today announced
second quarter financial results for 2023 and provided a corporate update on its development programs.
Ted
Raad, Chief Executive Officer of Pulmatrix commented,
“With our first quarter initiation of the PUR1900 Phase 2b study in allergic bronchopulmonary aspergillosis, or ABPA, our focus
for the second quarter was both to continue our work on the PUR1900 trial as well as to file an Investigational New Drug Application,
or IND, for a Phase 2 trial for PUR3100 for the treatment of acute migraine, which we achieved in June 2023. We anticipate starting the
PUR3100 trial once appropriate financing or partnerships have been arranged. While we advance all of our programs clinically, we have
focused on driving operational efficiencies and have extended our projected cash runway into the first quarter of 2025.”
Second
Quarter 2023 and Recent Program and Corporate Highlights
PUR1900
|
● |
PUR1900
is currently in a Phase 2 trial for the treatment of ABPA in patients with asthma (NCT05667662). In February 2023, Pulmatrix
began dosing patients for its proof-of-concept Phase 2b study of PUR1900 (itraconazole, administered as a dry powder for inhalation
using iSPERSE™). This Phase 2b trial is a randomized, double-blind, multi-center, placebo-controlled study to evaluate PUR1900’s
efficacy and safety. The multi-center study is being conducted in the United States, United Kingdom, Australia and France. Endpoints
include safety, tolerability, and potential efficacy outcomes to identify potential registrational endpoints in adult patients with
asthma and ABPA. Pulmatrix anticipates topline data from this study in the third quarter of 2024. |
PUR3100
|
● |
The
Company submitted an IND to the United States Food and Drug Administration for PUR3100 in June 2023. PUR3100 is under development
as an orally inhaled dihydroergotamine (DHE) engineered with iSPERSE™ for the acute treatment of migraine. The IND includes
a Phase 2 clinical protocol where safety and preliminary efficacy of PUR3100 will be investigated in patients with acute migraine.
The Company is pursuing potential partnership opportunities. |
|
|
|
|
● |
Data
from the Phase 1 study, completed last year, was presented at the American Headache Society 65th Annual Meeting in June 2023. Results
showed a lower incidence of nausea, and no vomiting was observed in PUR3100 dose groups compared to intravenously (IV) administered
DHE. The study also showed that PUR3100 achieved peak exposures in the targeted therapeutic range and time to maximum concentration
occurred at five minutes after dosing at all dosing levels. |
PUR1800
|
● |
In
February 2023, Pulmatrix presented complete results from a Phase 1b study of PUR1800 for acute exacerbations of chronic obstructive
pulmonary disease (AECOPD). The topline data was initially announced in March 2022, at the American Academy of Allergy, Asthma &
Immunology annual conference. The completed data analysis will inform the study design of a potential Phase 2 study in patients with
AECOPD. Pulmatrix plans to pursue partnership opportunities to advance PUR1800 into a potential Phase 2 clinical trial. |
Second
Quarter 2023 Financial Results
Revenues
increased $0.5 million to $1.8 million for the three months ended June 30, 2023 compared to $1.3 million for the three months ended June
30, 2022. The increase is related to the Company’s revenues recognized in accordance with the Cipla Agreement for PUR1900 during
the period.
Research
and development expenses decreased approximately $0.2 million to $4.2 million for the three months ended June 30, 2023 compared to $4.3
million for the three months ended June 30, 2022. The decrease was primarily due to decreased spend of $0.8 million in costs related
to the Company’s PUR3100 program and $0.1 million in costs related to the Company’s PUR1800 program, partially offset by
increases in spending of $0.5 million in costs related to the Company’s PUR1900 program and $0.2 million of employment and operating
costs.
General
and administrative expenses increased $0.1 million to $1.7 million for the three months ended June 30, 2023, compared to $1.6 million
for the three months ended June 30, 2022. The increase was primarily due to increased professional services costs.
Pulmatrix’s
total cash and cash equivalents balance as of June 30, 2023 was $25.8 million. The Company anticipates that its cash position, based
on operational efficiencies and prioritization of spending, is sufficient to fund its operations into the first quarter of 2025.
PULMATRIX,
INC.
Consolidated
Balance Sheets
(in
thousands, except share and per share data)
| |
June
30, 2023 | | |
December
31, 2022 | |
| |
(unaudited) | | |
| |
Assets | |
| | | |
| | |
Current assets: | |
| | | |
| | |
Cash and cash equivalents | |
$ | 25,791 | | |
$ | 35,628 | |
Restricted cash | |
| 153 | | |
| 153 | |
Accounts receivable | |
| 418 | | |
| 1,298 | |
Prepaid expenses and other current assets | |
| 1,019 | | |
| 1,068 | |
Total current assets | |
| 27,381 | | |
| 38,147 | |
Property and equipment, net | |
| 279 | | |
| 235 | |
Operating lease right-of-use asset | |
| 277 | | |
| 710 | |
Long-term restricted cash | |
| 1,472 | | |
| 1,472 | |
Other long-term assets | |
| 1,984 | | |
| 389 | |
Total assets | |
$ | 31,393 | | |
$ | 40,953 | |
Liabilities and stockholders’ equity | |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable | |
$ | 929 | | |
$ | 1,188 | |
Accrued expenses and other current liabilities | |
| 1,201 | | |
| 1,638 | |
Operating lease liability | |
| 358 | | |
| 857 | |
Deferred revenue | |
| 1,109 | | |
| 1,339 | |
Total current liabilities | |
| 3,597 | | |
| 5,022 | |
Deferred revenue, net of current portion | |
| 4,347 | | |
| 4,822 | |
Total liabilities | |
| 7,944 | | |
| 9,844 | |
Stockholders’ equity: | |
| | | |
| | |
Preferred stock, $0.0001 par value — 500,000 shares authorized; 6,746 shares designated Series A convertible preferred stock; no shares issued and outstanding at June 30, 2023 and December 31, 2022 | |
| - | | |
| - | |
Common stock, $0.0001 par value — 200,000,000 shares authorized; 3,652,285 and 3,639,185 shares issued and outstanding at June 30, 2023 and December 31, 2022, respectively | |
| - | | |
| - | |
Additional paid-in capital | |
| 305,189 | | |
| 304,585 | |
Accumulated deficit | |
| (281,740 | ) | |
| (273,476 | ) |
Total stockholders’ equity | |
| 23,449 | | |
| 31,109 | |
Total liabilities and stockholders’ equity | |
$ | 31,393 | | |
$ | 40,953 | |
PULMATRIX,
INC.
Consolidated
Statements of Operations
(in
thousands, except share and per share data)
(unaudited)
| |
Three
Months Ended June 30, | | |
Six
Months Ended June 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Revenues | |
$ | 1,844 | | |
$ | 1,331 | | |
$ | 3,343 | | |
$ | 2,491 | |
| |
| | | |
| | | |
| | | |
| | |
Operating expenses | |
| | | |
| | | |
| | | |
| | |
Research and development | |
| 4,165 | | |
| 4,337 | | |
| 8,039 | | |
| 8,486 | |
General and administrative | |
| 1,670 | | |
| 1,553 | | |
| 3,880 | | |
| 3,527 | |
Total operating expenses | |
| 5,835 | | |
| 5,890 | | |
| 11,919 | | |
| 12,013 | |
Loss from operations | |
| (3,991 | ) | |
| (4,559 | ) | |
| (8,576 | ) | |
| (9,522 | ) |
Other income (expense) | |
| | | |
| | | |
| | | |
| | |
Interest income | |
| 236 | | |
| 15 | | |
| 458 | | |
| 16 | |
Other expense, net | |
| (61 | ) | |
| (51 | ) | |
| (146 | ) | |
| (62 | ) |
Total other income (expense), net | |
| 175 | | |
| (36 | ) | |
| 312 | | |
| (46 | ) |
Net loss | |
$ | (3,816 | ) | |
$ | (4,595 | ) | |
$ | (8,264 | ) | |
$ | (9,568 | ) |
Net loss per share attributable to common stockholders – basic and diluted | |
$ | (1.04 | ) | |
$ | (1.36 | ) | |
$ | (2.26 | ) | |
$ | (2.87 | ) |
Weighted average common shares outstanding – basic and diluted | |
| 3,652,285 | | |
| 3,372,090 | | |
| 3,651,531 | | |
| 3,334,891 | |
About
Pulmatrix, Inc.
Pulmatrix
is a clinical-stage biopharmaceutical company developing innovative inhaled therapies to address serious pulmonary diseases and central
nervous system (“CNS”) disorders using its patented iSPERSE™ technology. The Company’s proprietary product pipeline
includes treatments for lung diseases, such as allergic bronchopulmonary aspergillosis (“ABPA”), Chronic Obstructive Pulmonary
Disease (“COPD”) and CNS disorders such as acute migraine. Pulmatrix’s product candidates are based on its proprietary
engineered dry powder delivery platform, iSPERSE™, which seeks to improve therapeutic delivery to the lungs by maximizing local
concentrations and reducing systemic side effects to improve patient outcomes.
For
more on our inhaled product candidates please visit: https://www.pulmatrix.com/pipeline.html.
Forward-Looking
Statements
Certain
statements in this press release that are forward-looking and not statements of historical fact are forward-looking statements within
the meaning of the federal securities laws. Such forward-looking statements include, but are not limited to, statements of historical
fact and may be identified by words such as “anticipates,” “assumes,” “believes,” “can,”
“could,” “estimates,” “expects,” “forecasts,” “guides,” “intends,”
“is confident that”, “may,” “plans,” “seeks,” “projects,” “targets,”
and “would,” and their opposites and similar expressions are intended to identify forward-looking statements. Such forward-looking
statements are based on the beliefs of management as well as assumptions made by and information currently available to management. Actual
results could differ materially from those contemplated by the forward-looking statements as a result of certain factors, including,
but not limited to, the impact of the novel coronavirus (COVID-19) on the Company’s ongoing and planned clinical trials; the geographic,
social and economic impact of COVID-19 on the Company’s ability to conduct its business and raise capital in the future when needed;
delays in planned clinical trials; the ability to establish that potential products are efficacious or safe in preclinical or clinical
trials; the ability to establish or maintain collaborations on the development of therapeutic candidates; the ability to obtain appropriate
or necessary governmental approvals to market potential products; the ability to obtain future funding for developmental products and
working capital and to obtain such funding on commercially reasonable terms; the Company’s ability to manufacture product candidates
on a commercial scale or in collaborations with third parties; changes in the size and nature of competitors; the ability to retain key
executives and scientists; the ability to secure and enforce legal rights related to the Company’s products, including patent protection.
A discussion of these and other factors, including risks and uncertainties with respect to the Company, is set forth in the Company’s
filings with the Securities and Exchange Commission, including its most recent Annual Report on Form 10-K, as may be supplemented or
amended by the Company’s Quarterly Reports on Form 10-Q and Current Reports on Form 8-K. The Company disclaims any intention or
obligation to revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required
by law.
Investor
Contact:
Timothy
McCarthy, CFA
917-679-9282
tim@lifesciadvisors.com
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