Indicate by check mark whether the registrant files or will file annual
reports under cover of Form 20-F or 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 July 1, 2026, Biophytis S.A. issued a press release announcing that
it reports its provisional financing results and provides its strategic outlook. A copy of the press release is attached as Exhibit 99.1
to this Form 6-K.
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.
Exhibit 99.1
BIOPHYTIS REPORTS
ITS PROVISIONAL FINANCIAL RESULTS
AND
PROVIDES ITS STRATEGIC OUTLOOK
Paris (France)
and Cambridge (Massachusetts, U.S.), July 1st, 2026, at 07:00am CET – Biophytis SA (Euronext Growth Paris: ALBPS), (“Biophytis”
or the “Company”), a clinical-stage biotechnology company specializing in the development of treatments for
age-related diseases, today reports its provisional, unaudited financial results for the fiscal year 2025 and provides an update on its
strategic outlook.
Stanislas Veillet,
Chairman and Chief Executive Officer of Biophytis, stated: “2025 was a transformative year for Biophytis. We successfully finalized
our strategic agreement with our Asian partners to establish a joint venture in Hong Kong, paving the way for the world’s first
Phase 3 clinical trial in sarcopenia. At the same time, we significantly strengthened our financial structure and enhanced our drug discovery
platform. These achievements position Biophytis to sustainably transform the lives of millions of patients living with sarcopenia and
obesity, while creating long-term value for our shareholders.”
Key Highlights
of 2025 and Early 2026
Execution of
the Company’s Asian Strategy in Sarcopenia
Following the entry
into exclusive negotiations with Chinese partners at the beginning of 2025 for the co-development of BIO101 in sarcopenia, Biophytis
successfully concluded these discussions with the signing of a memorandum of understanding to establish a Hong Kong-based joint venture,
Biophytis Biopharmaceutical Holding LTD, intended to accelerate the development and commercialization of BIO101 for sarcopenia across
Asian markets (China, South Korea and Japan).
Under this agreement,
the Asian partners have committed to invest up to US$20 million in the joint venture over a three-year period. On June 2, 2026,
Biophytis also announced the submission of the joint venture registration filing, a key milestone preceding the payment by the partners
of the first US$3 million tranche.
Major Regulatory
and Clinical Progress
During the year,
Biophytis achieved several key regulatory milestones across its flagship programs:
| § | SARA
Program in Sarcopenia: Following the receipt of the required approvals for its Phase
3 SARA-31 study in Europe (positive opinion from the EMA and authorization from the Belgian
competent authorities) and in the United States, Biophytis is actively pursuing the additional
regulatory approvals required in China and Japan to initiate the study, which is expected
to begin during the second half of 2026. |
| § | OBA
Program in Obesity: Biophytis received a positive opinion from the EMA on the first part
of its Phase 2 Clinical Trial Application and secured non-dilutive public funding from EMBRAPII
in Brazil, together with agreements with leading local clinical centers. The OBA study will
evaluate BIO101 in combination with GLP-1 receptor agonists (GLP-1 RAs), with the objective
of preserving muscle mass while promoting weight loss. |
The Company also
continued its active engagement with the scientific community to promote the potential of its lead drug candidate, BIO101, in preserving
muscle strength and mobility, notably during the ICFSR Congress held in March 2026.
Strengthening
the AI-Driven Drug Discovery Platform
Biophytis strengthened
its alliance with Lynx Analytics to accelerate the discovery of novel longevity-focused molecules through artificial intelligence. This
partnership aims to generate revenue through a computational longevity platform and new drug discovery approaches.
The Company also
participated in NVIDIA GTC in March 2026, illustrating its positioning at the intersection of biotechnology and artificial intelligence.
Reminder
of Biophytis’ Strategy
The Company’s
roadmap is structured around three strategic priorities:
| - | Launch
of the Phase 3 study in sarcopenia: Through its Asian joint venture, Biophytis intends
to initiate the Phase 3 clinical development of its SARA program, the first Phase 3 program
worldwide in this indication, to be conducted across Europe and Asia in order to address
the growing prevalence of sarcopenia and access the most attractive markets. |
| - | Launch
of the Phase 2 study in obesity: Biophytis intends to initiate the OBA study as soon
as possible to evaluate the efficacy of BIO101 in combination with GLP-1 receptor agonists
(GLP-1 RAs) in obese patients, with clinical development spanning the United States, Brazil
and Europe. |
| - | Strengthening
the research platform: Biophytis continues to modernize its research platform by integrating
disruptive technologies and artificial intelligence to accelerate the identification of new
drug candidates and the exploration of novel therapeutic targets. |
Financing
the Roadmap
Consistent with
its business model, the Company continues to actively pursue partnership agreements and collaborations across the Americas, Europe and
Asia, including the licensing and/or co-development agreements signed with Blanver for Latin America and the joint venture agreement
in China. Biophytis also continues to seek additional equity financing and to strengthen its financial structure, with the objective
of funding its research and development activities in its core indications (sarcopenia and obesity), as well as the modernization of
its drug discovery platform.
Update on
the Audit Process and Euronext Growth Listing
The 2025 statutory
financial information presented in this press release has been prepared by Management and constitutes provisional, unaudited financial
information, which remains subject to adjustment following the completion of the financial statement closing process and the audit procedures.
The financial closing process, preparation of the financial statements and compilation of the audit documentation are ongoing, and the
statutory auditors have commenced their audit procedures. The Company expects to publish its audited financial statements by the end
of July 2026, subject to the completion of the financial statements, the availability of all information required for the audit
procedures and the completion of the statutory auditors’ work.
The Company reminds
the market that trading in its shares on Euronext Growth Paris has been suspended since June 15, 2026, in accordance with applicable
market rules. This suspension results from the failure to publish the annual financial report for the fiscal year ended December 31,
2025 within the applicable regulatory deadline, due to operational delays in the preparation of the financial statements and the completion
of the audit. Trading on Euronext Growth Paris is expected to resume following the publication of the audited financial statements, by
the end of July 2026.
Biophytis SA is
reporting its provisional 2025 results in separate financial statements (PCG), in accordance with its listing status on Euronext Growth
and the small size of its group (total assets: <€20 million, workforce: <250 employees, no revenue for any of the group’s
entities). Although the scope differs from that of the IFRS consolidated financial statements published in 2024, and the 2025 provisional
data are not directly comparable, this presentation accurately reflects the Company’s economic reality and complies with Article L.
233-16 of the French Commercial Code.
A comparative table
is attached to ensure transparency.
| Amounts in € thousands | |
| Company | | |
| Consolidated | |
| Provisional and unaudited | |
| 31.12.2025 | | |
| 31.12.2025 | |
| Revenues | |
| - | | |
| - | |
| Net income | |
| -7 796 | | |
| -8 159 | |
| Equity | |
| -8 446 | | |
| 8 964 | |
Cash Position
and Going Concern
Provisional and
unaudited cash and cash equivalents amounted to €190 thousand as of December 31, 2025, compared with €72 thousand as of
December 31, 2024.
The Company’s
cash and cash equivalents are not sufficient to finance its operations over the next twelve months. Accordingly, there is a material
uncertainty regarding the Company’s ability to continue as a going concern.
As of the date
these provisional unaudited financial statements were approved and based on the refinancing transactions completed during the first half
of 2026, the Company’s current plans and assumptions, as well as the availability of the Hexagon bond financing facility once trading
has resumed, the Company believes that it will be able to finance its operations until September 30, 2026.
Shareholders’
Equity and Financing Transactions
During fiscal year
2025 and early 2026, Biophytis completed several transactions aimed at strengthening its shareholders’ equity and cash position
in order to support its short-term financial stability, including:
| - | January 8,
2025: €2.5 million cash injection, combined with a debt conversion of up to €6.1
million; |
| - | March 26,
2025: €2.6 million private placement with qualified investors; |
| - | August 2025:
establishment of a non-dilutive bond financing facility with Hexagon Capital Fund, with an
initial maximum amount of €1 million; |
| - | February 27,
2026: increase of the maximum amount available under the bond financing facility to €2
million, extending the Company’s cash runway by approximately four months; |
| - | March 11,
2026: capital increase generating gross proceeds of €2.02 million, together with the
full repayment of the variable-rate convertible debt held by Atlas in the amount of €1.02
million and the rescheduling of the €1.23 million Kreos Capital debt; |
| - | May 27,
2026: Biophytis signed an amendment to its bond financing facility with Hexagon Capital Fund,
making the €2 million drawing capacity renewable. This amendment optimizes the terms
of the existing facility by enhancing its financing capacity without increasing the overall
debt ceiling. |
Provisional
Unaudited Financial Debt and Current Liabilities
| Amounts in € thousands | |
Dec. 31, 2024 | | |
Dec. 31, 2025 | | |
| | |
| |
| | |
12 months | | |
12 months | | |
Change | |
| Bond borrowings | |
| 5 953 | | |
| 4272 | | |
| -1 681 | | |
| -28 | % |
| Current liabilities | |
| 6 439 | | |
| 7331 | | |
| 892 | | |
| 14 | % |
| Other current liabilities | |
| 115 | | |
| 341 | | |
| 226 | | |
| 197 | % |
| Total Financial Debt and Current Liabilities | |
| 12 506 | | |
| 11 944 | | |
| -562 | | |
| -4 | % |
Total financial
debt and current liabilities amounted to €12.5 million as of December 31, 2025, a decrease of €0.6 million (-5%) compared
with December 31, 2024. This change was primarily driven by a €1.7 million (-28%) reduction in bond debt, reflecting the financial
restructuring measures implemented by the Company, partially offset by a €0.9 million increase in current liabilities.
Provisional
Unaudited Operating Results
| Amounts in € thousands | |
Dec. 31, 2024 | | |
Dec. 31, 2025 | | |
| | |
| |
| | |
12 months | | |
12 months | | |
Change | |
| Revenue | |
- | | |
- | | |
| | |
| |
| Net research and development expenses | |
| -5 434 | | |
| -3 012 | | |
| 2 422 | | |
| -45 | % |
| General and administrative expenses | |
| -3 031 | | |
| -4 436 | | |
| -1 405 | | |
| 46 | % |
| Operating loss | |
| -8 465 | | |
| -7 447 | | |
| 1 018 | | |
| -12 | % |
| Financial expenses | |
| -1 493 | | |
| -642 | | |
| 851 | | |
| -57 | % |
| Financial income | |
| 572 | | |
| 293 | | |
| -279 | | |
| -49 | % |
| Financial result | |
| -921 | | |
| -349 | | |
| 572 | | |
| -62 | % |
| Net loss | |
| -9 386 | | |
| -7 796 | | |
| 1 590 | | |
| -17 | % |
Significant
Reduction in Operating Loss
Net loss amounted
to €7.8 million for the fiscal year ended December 31, 2025, compared with €9.4 million in 2024, representing an improvement
of €1.6 million (-17%). This improvement reflects the Company’s continued focus on controlling operating expenses, driven
by a reduction in net research and development expenses (-18%) and general and administrative expenses (-15%), as well as an improvement
in the financial result, primarily resulting from a significant decrease in financial expenses (-57%).
*
* *
About Biophytis
Biophytis SA is
a clinical-stage biotechnology company focused on developing drug candidates for age- related diseases. BIO101 (20-hydroxyecdysone),
our lead drug candidate, is a small molecule in development for muscular diseases (sarcopenia, Phase 3 ready to start) and metabolic
disorders (obesity, Phase 2 ready to start). The company is headquartered in Paris, France, with subsidiaries in Cambridge, Massachusetts,
USA, and Brazil. The Company’s ordinary shares are listed on Euronext Growth Paris (ALBPS - FR001400OLP5) and its ADS (American
Depositary Shares) are listed on the OTC market (BPTSY - US 09076G401). For more information, visit www.biophytis.com.
Biophytis
Contact
Investor relations
investors@biophytis.com
Media relations
Antoine Denry:
antoine.denry@taddeo.fr – +33 6 18 07 83 27
Nizar Berrada:
nizar.berrada@taddeo.fr – +33 6 38 31 90 50