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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): May 28, 2024
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.) |
36
Crosby Drive, Suite 100
Bedford,
MA 01730
(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 each 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
1.01 Entry into a Material Definitive Agreement.
On
May 28, 2024, Pulmatrix, Inc. (the “Company”) and MannKind Corporation, a Delaware Corporation
(“MannKind”) entered into a Bill of Sale and Assignment Agreement (the “BSA”)
with respect to the transfer of the Company’s Bedford, Massachusetts, R&D facility (the “R&D
Facility”) to MannKind along with all leasehold improvements, laboratory equipment and other related personal
property. In connection with the transfer of the R&D Facility, the Company, MannKind and Cobalt Propco 2020, LLC,
a Delaware limited liability company (the “Landlord”) will enter into an Amendment to Lease and Consent to
Assignment of Lease (the “Lease Assignment Agreement”) in connection with the premises (the
“Premises”) that the Company leases at 36 Crosby Drive, Bedford, Massachusetts, pursuant to that certain
Lease Agreement, dated as of January 7, 2022 (the “Lease Agreement”), by and between the Company and the
Landlord (collectively, the “MannKind Transactions”). Pursuant to the Lease Assignment Agreement, MannKind will
assume all of the Company’s obligations under the Lease Agreement, including all rent and other payments pursuant to the Lease
Agreement. The transfer of the R&D Facility to MannKind is expected to close during July 2024.
In
connection with the transactions contemplated by the BSA and Lease Assignment, the Company and MannKind entered into an Intellectual
Property Cross License Agreement (the “IPA”). The effectiveness of the IPA and the licenses granted therein
is subject to closing of the transactions contemplated by the BSA and the Lease Assignment Agreement. Pursuant to the IPA, the
Company will grant to MannKind (i) an exclusive license to develop, use, manufacture, market, offer and sell its inhaled Small Particles
Easily Respirable and Emitted (“iSPERSE”) formulations of Clofazimine, (ii) an exclusive license to develop,
use, manufacture, market, offer and sell formulations of iSPERSE with one more active pharmaceutical ingredients for the treatment of
nontuberculous mycobacteria lung disease in humans, (iii) an exclusive license to develop, use, manufacture, market, offer and sell iSPERSE
formulations of insulin, (iv) a non-exclusive license to develop, use, manufacture, market, offer and sell formulations of iSPERSE with
one more active pharmaceutical ingredients for the treatment of endocrine disease in humans, and (v) a non-exclusive license to develop,
use, manufacture, market, offer and sell formulations of iSPERSE with one more active pharmaceutical ingredients for the treatment of
interstitial lung diseases (including IPF, PPF and other related lung diseases) in humans. Additionally, pursuant to the IPA,
MannKind will grant to the Company (i) the exclusive right to develop, use, manufacture, market, offer and sell its “Cricket”
single-use disposable dry powder inhaler (including all modifications or improvement thereto made by or on behalf of the Company, the
“Cricket Device”) for the inhaled delivery of dihydroergotamine in any formulation whatsoever, including the
Company’s PUR3100 treatment of acute migraine and (ii) a non-exclusive license to develop, use, manufacture, market, offer and
sell the Cricket Device for the inhaled delivery of one more active pharmaceutical ingredients formulated with iSPERSE for the treatment
of neurological disease in humans.
Additionally,
pursuant to the Master Services Agreement, by and between the Company and MannKind, MannKind shall provide certain
development services to the Company, including but not limited to, activities to develop a dry powder formulation of the active
pharmaceutical ingredient that the Company provides to MannKind for oral inhalation using iSPERSE.
The
BSA, the IPA, the MSA and the Lease Assignment Agreement contain customary representation, warranties and indemnification provisions,
as applicable, and as related to transactions of this type.
Item
8.01 Other Events
On
May 29, 2024, the Company issued a press release announcing the MannKind Transactions, which is attached hereto as Exhibit
99.1 and incorporated herein by reference.
Item
9.01 Financial Statements and Exhibits.
(d)
Exhibits
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 hereunto duly authorized.
|
PULMATRIX,
INC. |
|
|
|
Date:
May 29, 2024 |
By: |
/s/
Teofilo Raad |
|
|
Teofilo
Raad |
|
|
Chief
Executive Officer |
Exhibit
99.1
Pulmatrix
Announces Cross License Agreement and Transfer of Laboratory to MannKind Corporation
Cross
license involves Pulmatrix iSPERSETM technology and MannKind’s Cricket® inhalation device.
Pulmatrix
transferring leased building, all leasehold improvements, laboratory equipment and other related personal property in exchange for MannKind
assumption of lease.
Master
service agreement in place for MannKind to provide future iSPERSETM dry powder drug formulation development services to Pulmatrix.
Bedford,
Mass., May 29, 2024 – Pulmatrix, Inc. (“Pulmatrix” or the “Company”) (Nasdaq: PULM),
a clinical-stage biopharmaceutical company developing innovative inhaled therapies to address serious central nervous system and pulmonary
diseases using its patented dry powder inhalation iSPERSE™ technology, today announced a series of transactions with MannKind Corporation
(Nasdaq: MNKD).
Ted
Raad, Chief Executive Officer of Pulmatrix, commented,
“MannKind’s interest in iSPERSETM validates the enablement potential of our innovative particle engineering
dry powder technology. In addition, the assumption of our lease and laboratory by MannKind helps extend our cash runway further into
2026. We are able to build upon this agreement to further support development of PUR3100 and its potential application with MannKind’s
Cricket® device to develop the 1st orally inhaled DHE treatment for acute migraine.”
The
Company entered into a cross license with MannKind pursuant to which MannKind will grant Pulmatrix a perpetual, royalty free,
exclusive license to use MannKind’s Cricket inhalation device for the inhaled delivery of PUR3100, our proprietary formulation
of dihydroergotamine (DHE) with iSPERSETM, and a perpetual, royalty free, non-exclusive license to use MannKind’s
Cricket inhalation device for the inhaled delivery of any dry powder formulation formulated for the treatment or prevention of
neurological disease. As part of the cross-license, the Company will grant MannKind a perpetual, royalty free, exclusive license to
formulate iSPERSETM with clofazimine for inhalation by humans for the treatment or prevention of infection, for the
treatment or prevention of nontuberculous mycobacteria lung disease in humans, and with insulin for inhalation by humans for the
treatment or prevention of diabetes. We will also grant MannKind a perpetual, royalty free, non-exclusive license to formulate
iSPERSETM for inhalation for the treatment or prevention of endocrine disease and for inhalation for the treatment or prevention
of interstitial lung diseases (including IPF, PPF and other related lung diseases) in humans (“ILD”).
As
part of the transaction, MannKind will assume the lease of our Bedford, Mass., R&D facility along with all leasehold improvements,
laboratory equipment and other related personal property used in the laboratory. To maintain continuity of iSPERSETM platform
knowledge, MannKind plans to hire some members of the Pulmatrix R&D staff.
The
agreements are anticipated to close in July 2024.
About
Pulmatrix, Inc.
Pulmatrix
is a clinical-stage biopharmaceutical company focused on the development of novel inhaled therapeutic products intended to prevent and
treat central nervous system (“CNS”), respiratory and other diseases with important unmet medical needs using its patented
iSPERSE™ technology. The Company’s proprietary product pipeline includes treatments for CNS disorders such as acute migraine
and serious lung diseases such as Chronic Obstructive Pulmonary Disease (“COPD”) and allergic bronchopulmonary aspergillosis
(“ABPA”). 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 the Company’s inhaled product candidates please visit:
https://www.pulmatrix.com/pipeline.html.
About
PUR3100
PUR3100
is an orally inhaled formulation of dihydroergotamine (DHE) engineered with iSPERSE™ for the treatment of acute migraine. The Phase
1 PUR3100 trial results were presented at the 65th Annual Meeting of the American Headache society in June 2023. Over 38 million patients
suffer from migraine in the United States and there is currently no orally inhaled DHE treatment option for patients.
About
iSPERSE™ Technology
Our
innovative particle engineering technology creates dry powder, which solves limitations of conventional inhaled technologies and expands
the universe of inhalable drug therapies. iSPERSETM is a proprietary technology that allows a broad range of drugs to be formulated
as small, dense, and dispersible particles for highly efficient drug delivery and deep penetration into the lungs. iSPERSETM
can efficiently deliver small molecules, drug combinations, peptides, proteins, and nucleic acids via the respiratory system for the
treatment of both respiratory and non-respiratory diseases.
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 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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