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
UNDER THE SECURITIES EXCHANGE ACT OF 1934
Date of report: September 28, 2023
Commission File Number: 001-38974
BIOPHYTIS S.A.
(Translation of registrant’s name into
English)
Stanislas Veillet
Biophytis S.A.
Sorbonne University—BC 9, Bâtiment
A 4ème étage
4 place Jussieu
75005 Paris, France
+33 1 44 27 23 00
(Address of principal executive office)
Indicate by check mark whether the registrant files or will file annual
reports under cover of Form 20-F or Form 40-F:
x 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): ¨
On September 25, 2023, Biophytis S.A. issued a press release
announcing that Biophytis and Skyepharma have signed a Partnership Agreement for the Production of Sarconeos (BIO101). A copy of the
press release is attached as Exhibit 99.1 to this Form 6-K.
EXHIBIT LIST
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.
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BIOPHYTIS S.A. |
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Date: September 28, 2023 |
By: |
/s/ Stanislas Veillet |
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Name: Stanislas Veillet |
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Title: Chairman and Chief Executive Officer |
Exhibit 99.1
Press
Release
Biophytis and
Skyepharma sign a Partnership Agreement for the Production of Sarconeos (BIO101)
Paris (France)
and Cambridge (Massachusetts, USA), September 25, 2023 – 07:00 am CET – Biophytis SA (Nasdaq CM : BPTS, Euronext
Growth Paris : ALBPS), («Biophytis»), a clinical-stage biotechnology company specialized in the development of therapeutics
that are aimed at slowing the degenerative processes associated with aging and improving functional outcomes for patients suffering from
age-related diseases, and Skyepharma, a French pharmaceutical company specializing in the formulation, development and production
of pharmaceutical products, announce the signature of a partnership agreement for the production of regulatory batches of Sarconeos (BIO101)
for severe forms of Covid-19, with a view to the submission of marketing authorization applications.
Based on the active
ingredient produced by SEQENS, Skyepharma will develop finished product batches meeting the GMP (Good Manufacturing Practice) standards
required for market access filings. The key stages in the production of Sarconeos (BIO101) will be entrusted to leading, innovative French
partners meeting the highest standards of pharmaceutical quality. Pharmaceutical development work at the industrial stage will complete
the information required for early access authorizations, particularly in France and Brazil.
Stanislas Veillet,
CEO of Biophytis, states: "Following on from the framework contract signed with SEQENS in July for the production of
Sarconeos active ingredient (BIO101), this new partnership is a key step for Biophytis as it secures the production of finished product
batches of its leading drug candidate, and thus continues our efforts to access our targeted markets."
David Lescuyer,
CEO of Skyepharma, added: "We are delighted to be working alongside Biophytis to develop the regulatory batches for Sarconeos
(BIO101). We are also proud to have approvals from the world's leading health agencies - the FDA in the United States, the EMA in Europe
and ANVISA in Brazil - enabling us to ensure the marketing and commercial production of Sarconeos (BIO101) in these countries. For us,
it's a question of putting our expertise at the service of ambitious projects capable of solving major public health issues."
***
About BIOPHYTIS
Biophytis SA is
a clinical-stage biotechnology company specializing in the development of drug candidates for age-related diseases. Sarconeos (BIO101),
our lead drug candidate, is a small molecule in development for age-related neuromuscular (sarcopenia and Duchenne muscular dystrophy)
and cardiorespiratory (Covid-19) diseases. Promising clinical results were obtained in the treatment of sarcopenia in an international
phase 2 study, enabling the launch of a phase 3 study in this indication (SARA project). The safety and efficacy of Sarconeos (BIO101)
in the treatment of severe COVID-19 were studied in a positive international phase 2-3 clinical trial (COVA project). A pediatric formulation
of Sarconeos (BIO101) is currently being developed for the treatment of Duchenne Muscular Dystrophy (DMD, MYODA project). The company
is based in Paris, France, and Cambridge, Massachusetts. The Company's ordinary shares are listed on Euronext Growth (Ticker: ALBPS -ISIN:
FR0012816825) and the ADSs (American Depositary Shares) are listed on Nasdaq Capital Market (Ticker BPTS - ISIN: US09076G1040).
For more information,
visit www.biophytis.com
About SKYEPHARMA
Skyepharma is an
independent French pharmaceutical CDMO company, 100% owned by its management team and Bpifrance. Skyepharma specializes in the formulation,
development and production of oral pharmaceutical products (tablets, capsules, powders), with particular expertise and proprietary technologies
for complex and modified-release forms. Skyepharma is based in Saint-Quentin-Fallavier (Isère), near Lyon international airport.
Skyepharma develops and manufactures drugs for international clients, supported by proprietary technologies and a site certified by the
European (ANSM), American (FDA) and Brazilian (ANVISA) authorities, among others.
Through Skyehub
Bioproduction, Skyepharma also offers clinical and commercial production capabilities dedicated to biomedical companies.
For further information,
visit www.skyepharma.com
Disclaimer
This press
release contains forward-looking statements. Forward-looking statements include all statements that are not historical facts. In
some cases, you can identify these forward-looking statements by the use of words such as "outlook,"
"believes," "expects," "potential," "continues," "may," "will,"
"should," "could," "seeks," "predicts," "intends," "trends,"
"plans," "estimates," "anticipates" or the negative version of these words or other comparable
words. Such forward- looking statements are based on assumptions that Biophytis considers to be reasonable. However, there can
be no assurance that the statements contained in such forward-looking statements will be verified, which are subject to various
risks and uncertainties. The forward-looking statements contained in this press release are also subject to risks not yet known to
Biophytis or not currently considered material by Biophytis. Accordingly, there are or will be important factors that could cause
actual outcomes or results to differ materially from those indicated in these statements. Please also refer to the "Risk and
uncertainties the Company is to face» section from the Company's 2022 Financial Report available on BIOPHYTIS website
(www.biophytis.com) and as exposed in the "Risk Factors" section of form 20-F as well as other forms filed with the SEC
(Securities and Exchange Commission, USA). We undertake no obligation to publicly update or review any forward-looking statement,
whether as a result of new information, future developments or otherwise, except as required by law.
Biophytis contacts
Investor relations
Nicolas Fellmann,
CFO
Investors@biophytis.com
Media
Antoine Denry: antoine.denry@taddeo.fr –
+33 6 18 07 83 27
Nizar Berrada: nizar.berrada@taddeo.fr
– +33 6 38 31 90 50
Skyepharma contacts
Media &
Investor Relations
Laurent Rigaudeau, Chief Business Officer
l.rigaudeau@skyepharma.com
+33 6 30 49 22 82
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