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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 15, 2024
PaxMedica, Inc.
(Exact name of registrant as specified in its
charter)
Delaware |
001-41475 |
85-0870387 |
(State or other jurisdiction
of incorporation) |
(Commission File Number) |
(IRS Employer
Identification No.) |
303 South Broadway, Suite 125
Tarrytown, NY |
10591 |
(Address of principal executive offices) |
(Zip Code) |
(914) 987-2876
(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 (see General Instructions A.2.
below):
¨ |
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 Exchange Act:
Title of each class |
|
Trading
Symbol(s) |
|
Name of each exchange
on which registered |
Common Stock, par value $0.0001 per share |
|
PXMD |
|
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 x
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 8.01 Notice to Appeal Delisting.
On May 15, 2024, PaxMedica, Inc. (the
“Company”) issued a press release announcing that PaxMedica Filed Nasdaq Delisting Appeal Notice and
Prepares for Upcoming FDA Meeting on PAX-101.
Item 9.01 Financial Statements and
Exhibits.
(d) Exhibits –
The following exhibits are filed as part of this report:
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.
|
PaxMedica, Inc. |
|
|
|
|
By: |
/s/ Howard J. Weisman |
|
Names: Howard J. Weisman |
|
Title: Chief Executive Officer |
Date: May 15, 2024
Exhibit 99.1
PaxMedica Files Nasdaq Delisting Appeal Notice
and Prepares
for Upcoming FDA Meeting on PAX-101
TARRYTOWN, NY / ACCESSWIRE / May 15, 2024 / PaxMedica, Inc. (the
“Company” or “PaxMedica”)(OTC:PXMD), a biopharmaceutical company dedicated to advancing treatments for neurological
disorders, today announced it has timely filed a formal notice of appeal with the Nasdaq Office of Appeals and Review to reverse the decision
of a Nasdaq Hearings Panel to delist the Company from Nasdaq. Following receipt of notification from Nasdaq on April 30th, PaxMedica determined
to appeal the decision and intends to maintain that the Hearings Panel did not consider sufficiently or appropriately crucial aspects
of PaxMedica’s recent achievements and ongoing actions to regain compliance with all applicable requirements for continued listing.
PaxMedica has retained Jacob Frenkel, Dickinson Wright, PLLC as its lead counsel in the appeal, working with the consulting firm that
interacted previously with the Hearings Panel.
Howard Weisman, CEO of PaxMedica, commented, "We are seeking a
reevaluation of Nasdaq’s recent action based on new developments that underscore our ongoing progress and commitment to addressing
global health challenges. Notably, following our announcements on the completion of registration lots of PAX-101 in mid-April, the Company
just submitted a briefing book for an important FDA Type C meeting scheduled for June 27th, during which we will present key updates on
our plans for NDA submission later this year. We believe this, as well as our financing plans which we made known to the Hearings Panel,
support persuasively our arguments to appeal and restore trading on Nasdaq."
Recent milestones for PaxMedica include:
|
· | April 11th: Completion of three pivotal registration/validation batches of PAX-101, an IV formulation of suramin, crucial for ongoing regulatory submissions. |
| · | April 16th: Receipt of an urgent request from Malawi’s Ministry
of Health for emergency access to suramin to address a looming humanitarian crisis due to the scarcity of treatment for TBr HAT, a fatal
form of African Sleeping Sickness. |
| | |
| · | April 23rd: Agreement to supply Malawi with PAX-101 from our stock,
reinforcing our role in combating global health emergencies. |
| | |
| · | May 10th: PaxMedica submits FDA Briefing Book for June
27, 2024, Type C meeting. |
Weisman stated "these actions not only demonstrate our
operational effectiveness, but also our vital role in the global healthcare landscape. We are encouraged that the upcoming FDA meeting,
and our continuous efforts to supply life-saving treatments, will result in favorable consideration by Nasdaq in our appeal." Nevertheless,
PaxMedica acknowledges that it cannot predict the outcome of the appeal. Weisman added that “we are committed to advancing expeditiously
our efforts to maximize shareholder opportunities and value and pursue approval of our solutions for neurological disorders.”
PaxMedica
remains resolute in its mission to develop and provide innovative treatments for neurological disorders, ensuring significant contributions
to public health worldwide. For more information on PaxMedica’s ongoing initiatives and developments, please visit www.paxmedica.com.
About
PaxMedica
PaxMedica,
Inc. is a forward-looking clinical-stage biopharmaceutical firm specializing in cutting-edge anti-purinergic drug therapies (APT) aimed
at addressing a range of challenging neurologic disorders. Our comprehensive portfolio encompasses a spectrum of conditions, including
neurodevelopmental disorders such as Autism Spectrum Disorder (ASD), as well as other critical areas within the neurology field. Additionally,
we intend to provide the rest of the world with an additional, reliable source of suramin, the accepted standard of care for Stage 1,
Trypanosoma Brucei Rhodesiense.
We
are dedicated to the continuous development and evaluation of our pioneering program, PAX-101, an intravenous suramin formulation that
lies at the heart of our efforts, particularly focused on innovative ASD treatment solutions. Our ongoing research initiatives not only
prioritize the needs of ASD patients, but also extend to exploring potential therapeutic applications for related conditions. To learn
more about our transformative work, please visit www.paxmedica.com.
Interested
investors and shareholders are encouraged to sign up for press releases and industry updates by registering for Email Alerts at https://www.paxmedica.com/email-alerts and
by following PaxMedica on Twitter and LinkedIn.
Forward-Looking
Statements
This
press release contains “forward-looking statements.” Forward-looking statements reflect our current view about future events.
Investors can identify these forward-looking statements by words or phrases such as “may,” “will,” “could,”
“expect,” “anticipate,” “aim,” “estimate,” “intend,” “plan,”
“believe,” “is/are likely to,” “propose,” “potential,” “continue” or similar
expressions. These forward-looking statements include our anticipated clinical program, the timing and success of our anticipated data
announcements, pre-clinical and clinical trials and regulatory filings, and distribution and demand for our product candidates. These
forward-looking statements involve known and unknown risks and uncertainties and are based on the Company’s current expectations
and projections about future events that the Company believes may affect its financial condition, results of operations, business strategy
and financial needs. Such risks and uncertainties include, but are not limited to, risks associated with the Company’s development
work, including any delays or changes to the timing, cost and success of the Company’s product development and clinical trials,
risk of insufficient capital resources, cash funding and cash burn, regulatory approvals and risks associated with intellectual property
and infringement claims. The Company undertakes no obligation to update or revise publicly any forward-looking statements to reflect
subsequent occurring events or circumstances, or changes in its expectations, except as may be required by law. Although the Company
believes that the expectations expressed in these forward-looking statements are reasonable, it cannot assure you that such expectations
will turn out to be correct, and the Company cautions investors that actual results may differ materially from the anticipated results
and encourages investors to review other factors that may affect its future results described in the Company’s “Risk Factors”
section and other sections in its most recent Annual Report on Form 10-K, and subsequent quarterly and other filings with the U.S. Securities
and Exchange Commission.
Contacts
PaxMedica,
Inc.
303 S Broadway,
Suite 125.
Tarrytown, NY 10591
www.paxmedica.com
Media
Contact
media@paxmedica.com
Investor
Contact
Scott McGowan
InvestorBrandNetwork (IBN)
Phone: 310.299.1717
ir@paxmedica.com
www.paxmedica.com/investors
SOURCE: PaxMedica,
Inc.
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