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Biophytis Extends Its Contract With Atlas to Secure Financing for Its Business Activities

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Biophytis has extended its bond financing agreement with Atlas, allowing for the issuance of convertible bonds up to €16 million over two years. This extension aims to fund Biophytis' clinical programs in obesity (OBA) and Duchenne Muscular Dystrophy (MYODA). However, the financing method may cause significant shareholder dilution and downward pressure on the stock price. Biophytis’ OBA Phase 2 study is set to start in mid-2024, and the MYODA trial has received FDA approval. The company is also seeking additional partners and funding to support these programs.

Positive
  • Extended bond financing agreement up to €16 million.
  • Funding secured for clinical programs in obesity and Duchenne Muscular Dystrophy.
  • OBA Phase 2 study to start mid-2024.
  • MYODA trial received FDA approval.
Negative
  • Significant shareholder dilution expected.
  • Potential downward pressure on the stock price.
  • Risks associated with the non-completion of all financing tranches.
  • Volatility and liquidity risks due to share sales.

The extension of Biophytis' bond financing agreement with Atlas facilitates the company's financial stability and operational continuity, particularly for their clinical programs. However, the structure of this financing deal, which involves the issuance of convertible bonds, has potential dilutive effects on existing shareholders. Dilutive financing, where bonds can convert into shares, often leads to an increase in the number of outstanding shares, thereby reducing the value of each existing share.

The agreement stipulates that new tranches of up to €2 million can be issued only if the outstanding bond debt held by Atlas is no more than €2 million, which is a measure to limit excessive dilution. However, as Atlas intends to sell the shares resulting from bond conversions quickly, it could cause immediate downward pressure on the stock price. This means that while Biophytis can secure necessary funds, shareholders may experience significant value loss and volatility in their investments.

For retail investors, it’s important to recognize that while this financing can extend the company's cash runway and fund critical R&D, the inherent risks include potential stock price drops and dilution, which may lead to reduced returns in the short term.

The market dynamics for Biophytis’ targeted diseases are worth noting. The obesity treatment market is projected to grow significantly, with an estimated market size reaching $100 billion by 2030 from $6 billion in 2023. This highlights a substantial growth opportunity for Biophytis, particularly if their OBA clinical program proves successful. Similarly, the orphan drug designation and FDA approval for their MYODA program targeting Duchenne Muscular Dystrophy (DMD) present a potential fast-track to market for a disease area with high unmet needs.

Despite the positive market potential, retail investors should be aware of the risks associated with the company’s reliance on dilutive financing. The quick sale of converted shares by Atlas could increase stock volatility and impact liquidity. Investors should weigh these market opportunities against the financial risks and ensure they have a clear understanding of the potential dilution and its effects on their holdings.

Important note: Biophytis has set up financing in the form of Bonds redeemable in cash and in new and existing shares (ORNANE) with the company Atlas, which, after having received the shares resulting from the conversion or exercise of these instruments, is not intended to remain a shareholder of the company. The shares resulting from the conversion of the above-mentioned securities will, in general, be sold on the market very quickly, which may create downward pressure on the share price. Shareholders may suffer a loss of their invested capital due to a significant decrease in the value of the company's stock, as well as significant dilution due to the large number of securities issued to the benefit of the Atlas company. Investors are advised to be vigilant before making the decision to invest in the securities of the company admitted to trading which carries out such dilutive financing transactions, particularly when they are carried out successively. Investors are particularly invited to take note of the risks relating to these operations, mentioned in the press release below.

PARIS, FRANCE AND CAMBRIDGE, MA / ACCESSWIRE / June 19, 2024 / BiophytisSA (Euronext Growth Paris:ALBPS), ("Biophytis" or the "Company"), a clinical-stage biotechnology company specialized in the development of therapeutics for age-related diseases, announces the extension of its bond financing agreement with Atlas, a specialized investment fund based in New York (USA), in order to secure financing for its business activities, in particular the launch of its clinical programs OBA in obesity and MYODA in Duchenne Muscular Dystrophy (DMD).

This two-year amendment, expiring on 14 June 2026, will allow Biophytis to issue convertible bonds for a maximum amount of €16 million, in tranches of up to €2 million each. The extension of this financing facility and the terms of the renewal agreement reflect Atlas‘ confidence in Biophytis' growth potential. To limit the potentially dilutive impact of the financing, the issue of a new tranche will only be possible if the outstanding bond debt held by Atlas at the time of the drawdown is no more than €2 million. The current outstanding amount is €3 million. Given the characteristics of the contract amendment, this financing facility could extend the Company's cash runway, currently estimated at the end of August 2024, to the end of 2024 and contribute to the financing of R&D programs in 2025.

With an estimated market size of $6 billion in 2023 and an estimated average annual growth rate expected around 42%, the addressable market for the treatment of obesity is set to reach $100 billion by 2030. The OBA Phase 2 clinical study is expected to start mid-2024, upon regulatory approvals, with first patients expected to be treated in the second half of 2024.

In addition, Biophytis has been granted orphan drug designation and has received IND (Investigational New Drug) approval from the FDA (Food and Drug Administration) to start the MYODA phase 1/2 clinical trial with BIO101 (20-hydroxyecdysone) in non-ambulatory DMD patients. This terrible neuromuscular disease with no approved treatment for the specific respiratory symptoms is an opportunity for a fast access to market.

Biophytis is actively seeking partners and additional funding to conduct its OBA and MYODA clinical programs in the coming months.

Features of the Atlas 2021 Contract Amendment

Legal framework

The securities issued will give Atlas access, immediately or in the future, to the Company's share capital, with cancellation of preferential subscription rights in favour of a category of persons, in accordance with Article L. 225-129 et seq. of the French Commercial Code.

In accordance with the delegation of powers granted by the General Meeting of Shareholders of 2 April 2024, the Chief Executive Officer signed the amendment to the Atlas 2021 Agreement on the basis of a delegation of powers granted by the Company's Board of Directors.

This offer of financial securities did not give rise to a prospectus subject to approval by the Autorité des Marchés Financiers (AMF).

The Company keeps its shareholders informed of the exercise of the ORNANE bonds and subsequent conversions, in the form of a table summarizing the ORNANE bonds and the number of outstanding shares, which can be consulted on the Company's website. This table presents the history of the use of the ORNANE line as part of the Atlas 2021 contract.

Main characteristics of the ORNANE bonds

The ORNANE bonds, with a nominal value of €25,000, may be issued subject to a period of 40 trading days between each issue and up to a maximum amount of €2 million, each issue constituting a tranche.A tranche may be issued if the outstanding bond debt held by Atlas does not exceed €2 million. The ORNANE bonds will not bear interest and will have a maturity of 24 months from the date of issue.

The holder will have the option to request redemption of the ORNANE bonds at any time during the maturity period, and the Company will have the right to redeem the ORNANE bonds in cash. In the event of redemption in cash, the amount to be redeemed will be limited to 110% of the principal amount.

At the end of the maturity period, and in the event that the ORNANE bonds have not been redeemed either in cash or in new or existing shares, the holder will have the obligation to convert the ORNANE bonds.

The holder will be able to request conversion of the ORNANE bonds at any time in accordance with the conversion ratio determined by the following formula: N = Vn / (R x P), where

- "N" is the number of shares resulting from the conversion,

- "Vn" is the nominal value of the ORNANE bonds, i.e. 25,000 euros each,

- "R"' is the conversion ratio, i.e. 1.00,

- "P" is the conversion price, i.e. the lowest weighted average price for the 10 trading days preceding the conversion request date.

On the date of the conversion request, the Company will have the option of redeeming the ORNANE bonds in cash in accordance with the following formula: V = (Vn / P) * Pr, where

- "V" is the amount to be reimbursed to the bearer.

- "Pr" is the revised price.

The revised price is the lower of (i) the weighted average closing price for the 10 trading days preceding the conversion request and (ii) P*1.10.

The ORNANE bonds may only be sold by their holder to affiliated companies and will not be the subject of a request for admission to trading on the Euronext Growth market.

Number of shares and dilution (modelling)

On the basis of 5,254,245 outstanding shares, and assuming an issue followed by conversion of a tranche of €2 million, then of all the tranches on 14 June 2024, and a conversion price equal to 0.65 euro, the impact of the issue on the shareholding of a shareholder holding 1% of the Company's capital prior to the transaction would be as follows:

Impact of the issue on the shareholding of a shareholder holding 1% of the capital before the transaction

Non-diluted basis

Diluted basis

Before the issue of ORNANE bonds

1.00%

0.41%

On the basis of conversion of a tranche of ORNANE bonds under the amendment to the Atlas 2021 contract: issue of 3,076,923 new shares

0.59%

0.32%

On the basis of conversion of all the ORNANE bonds under the amendment to the Atlas 2021 Contract: issue of 24,615,385 new shares

0.15%

0.13%

Risk factors

  • Dilution risk: the shareholders of the Company, who cannot participate in the operation, will suffer dilution when issuing new shares in conversion of convertible bonds;
  • Risk in the event of non-completion of all tranches: the total amount of the OC issue is not guaranteed and will depend in particular on market conditions, so the company may be required to seek additional financing;
  • Risk of volatility and liquidity of the Company's shares: the sale of shares on the market could have significant consequences on the volatility and liquidity of the security;
  • Risk relating to changes in the stock price: as the intermediary is not intended to remain a shareholder, the transfers of new shares issued upon conversion of the OCs could have an unfavorable impact on the company's share price.

****

About BIOPHYTIS
Biophytis SA is a clinical-stage biotechnology company specializing in the development of drug candidates for age-related diseases. BIO101 (20-hydroxyecdysone), our lead drug candidate, is a small molecule in development for muscular (sarcopenia, phase 3 ready and Duchenne muscular dystrophy), respiratory (Covid-19 phase 2-3 completed) and metabolic diseases (obesity, phase 2 to be started). 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 OTC market (Ticker: BPTSY - ISIN: US09076G4010). For more information, visit www.biophytis.com

Forward-Looking Statements
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 thesewords 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 2023 FinancialReport available on BIOPHYTIS website 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 because 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

SOURCE: Biophytis



View the original press release on accesswire.com

FAQ

What is the impact of Biophytis' new financing agreement with Atlas?

The agreement allows Biophytis to issue convertible bonds up to €16 million over two years to fund clinical programs but may lead to shareholder dilution and stock price pressure.

How will Biophytis' financing agreement affect BPTS shareholders?

Shareholders may experience significant dilution and a decrease in stock value due to the issuance of new shares as part of the financing.

What clinical programs will Biophytis fund with the new financing?

Biophytis plans to fund its OBA program for obesity and MYODA program for Duchenne Muscular Dystrophy with the new financing.

When is the OBA Phase 2 clinical study expected to start?

Biophytis' OBA Phase 2 study is expected to start in mid-2024, pending regulatory approvals.

What is the current outstanding bond debt held by Atlas?

The current outstanding bond debt held by Atlas is €3 million.

What are the risks associated with Biophytis' financing strategy?

The risks include significant shareholder dilution, potential stock price pressure, volatility, liquidity issues, and the possibility of requiring additional financing.

How does the financing agreement impact Biophytis' cash runway?

The financing agreement could extend Biophytis' cash runway from the end of August 2024 to the end of 2024.

What is the estimated market size for obesity treatments Biophytis is targeting?

The market size for obesity treatments is estimated to reach $100 billion by 2030, with a growth rate of around 42%.

What approval has Biophytis received for the MYODA clinical trial?

Biophytis has received FDA IND approval to start the MYODA Phase 1/2 clinical trial with BIO101 for non-ambulatory Duchenne Muscular Dystrophy patients.

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