STOCK TITAN

Soligenix Announces Reverse Stock Split

Rhea-AI Impact
(High)
Rhea-AI Sentiment
(Positive)
Rhea-AI Summary

Soligenix (NASDAQ: SNGX) announced a reverse stock split at a 1-for-16 ratio, effective at 4:00 p.m. on June 5, 2024. Trading on a split-adjusted basis will begin June 6, 2024. The reverse split will reduce the number of outstanding shares from approximately 15.8 million to around 987,490 shares. Stockholders' equity percentage remains unchanged, and fractional shares will be rounded up. No new stock certificates are required, but proportional adjustments will be made to equity awards and warrants. Stockholders with brokerage accounts will see automatic adjustments. The new CUSIP number is 834224 604.

Positive
  • Reverse stock split can help improve the stock price and meet NASDAQ listing requirements.
  • Reduction in outstanding shares from approximately 15.8 million to 987,490 shares.
  • Stockholders' percentage equity remains unchanged post-split.
  • Proportional adjustments to equity awards and warrants maintain value for option holders.
Negative
  • Reverse stock splits can sometimes reflect underlying financial instability.
  • Potential for decreased liquidity with fewer shares outstanding.
  • Stock price may experience volatility due to the reverse split.
  • Risk of shareholder dilution due to future equity-related actions.

Insights

Soligenix's decision to implement a 1-for-16 reverse stock split primarily aims at increasing the share price by reducing the number of outstanding shares. This move is often used to meet the minimum bid price requirement for continued listing on the NASDAQ, signaling potential challenges the company faces in maintaining its listing status. However, a reverse stock split does not impact the intrinsic value of the company, but it can affect investor perception.

In the short-term, the reverse split might lead to increased volatility due to speculative trading. Some investors might interpret the split negatively, as it can be seen as a company struggling with its stock price. Conversely, it can also attract institutional investors who have mandates to avoid stocks trading under a certain price.

Long-term, the effectiveness of the reverse split will largely depend on Soligenix's underlying business performance. If the company can demonstrate strong growth prospects and deliver on its pipeline, the reverse split could prove beneficial by making the stock more attractive. However, if poor financial performance continues, the reverse split might only serve as a temporary fix.

Retail investors should monitor how the market reacts post-split and consider the company's fundamentals before making any decisions.

A reverse stock split can sometimes be a double-edged sword for companies like Soligenix. On the one hand, reducing the number of outstanding shares can give the stock a higher price per share, potentially meeting NASDAQ’s listing requirements and making the stock appear more attractive to some investors. However, it’s important to understand that this is a cosmetic change and does not alter the market capitalization or the underlying business's value.

For retail investors, it’s essential to look beyond the share price. The company's ability to develop and commercialize its pipeline effectively will be the true determinant of value. Moreover, the biopharmaceutical sector is highly competitive and companies must continuously innovate and secure regulatory approvals to maintain and grow their market position.

Investors should keep an eye on upcoming clinical trials, FDA approvals and any potential partnerships or acquisitions that Soligenix might engage in. These factors will likely have a more substantial impact on stock performance than the reverse split itself.

Overall, the reverse split is a strategic move but not a definitive indicator of future performance.

Common Stock Will Begin Trading on Split-Adjusted Basis on June 6, 2024

PRINCETON, N.J., May 31, 2024 /PRNewswire/ -- Soligenix, Inc. (NASDAQ: SNGX) (Soligenix or the Company), a late-stage biopharmaceutical company focused on developing and commercializing products to treat rare diseases where there is an unmet medical need, announced today that it intends to effect a reverse stock split of its common stock at a ratio of 1 post-split share for every 16 pre-split shares. The reverse stock split will become effective at 4:00 p.m. on Wednesday, June 5, 2024. Soligenix's common stock will continue to be traded on The Nasdaq Capital Market under the symbol SNGX and will begin trading on a split-adjusted basis when the market opens on Thursday, June 6, 2024. The new CUSIP number for the Company's common stock following the reverse stock split will be 834224 604.

At the 2024 Annual Meeting of Stockholders initially convened on May 23, 2024 and reconvened on May 30, 2024, Soligenix's stockholders granted the Company's Board of Directors the discretion to effect a reverse stock split of Soligenix's common stock through an amendment to its Second Amended and Restated Certificate of Incorporation at a ratio of not less than 1-for-2 and not more than 1-for-20, with such ratio to be determined by the Company's Board of Directors.

At the effective time of the reverse stock split, every 16 shares of Soligenix's issued and outstanding common stock will be converted automatically into one issued and outstanding share of common stock without any change in the par value per share. Stockholders holding shares through a brokerage account will have their shares automatically adjusted to reflect the 1-for-16 reverse stock split. It is not necessary for stockholders holding shares of the Company's common stock in certificated form to exchange their existing stock certificates for new stock certificates of the Company in connection with the reverse stock split, although stockholders may do so if they wish.

The reverse stock split will affect all stockholders uniformly and will not alter any stockholder's percentage interest in the Company's equity, except to the extent that the reverse stock split would result in a stockholder owning a fractional share. Any fractional share of a stockholder resulting from the reverse stock split will be rounded up to the nearest whole number of shares. The reverse stock split will reduce the number of shares of Soligenix's common stock outstanding from 15,799,837 shares to approximately 987,490 shares, subject to adjustment for the rounding up of fractional shares. Proportional adjustments will be made to the number of shares of Soligenix's common stock issuable upon exercise or conversion of Soligenix's equity awards and warrants, as well as the applicable exercise price. Stockholders with shares in brokerage accounts should direct any questions concerning the reverse stock split to their broker; all other stockholders may direct questions to the Company's transfer agent, Equiniti Trust Company, LLC, toll-free at (877) 248-6417 or at (718) 921-8317.

About Soligenix, Inc.

Soligenix is a late-stage biopharmaceutical company focused on developing and commercializing products to treat rare diseases where there is an unmet medical need. Our Specialized BioTherapeutics business segment is developing and moving toward potential commercialization of HyBryte(SGX301 or synthetic hypericin sodium) as a novel photodynamic therapy utilizing safe visible light for the treatment of cutaneous T-cell lymphoma (CTCL). With successful completion of the second Phase 3 study, regulatory approvals will be sought to support potential commercialization worldwide. Development programs in this business segment also include expansion of synthetic hypericin (SGX302) into psoriasis, our first-in-class innate defense regulator (IDR) technology, dusquetide (SGX942) for the treatment of inflammatory diseases, including oral mucositis in head and neck cancer, and (SGX945) in Behçet's Disease.

Our Public Health Solutions business segment includes development programs for RiVax®, our ricin toxin vaccine candidate, as well as our vaccine programs targeting filoviruses (such as Marburg and Ebola) and CiVax, our vaccine candidate for the prevention of COVID-19 (caused by SARS-CoV-2). The development of our vaccine programs incorporates the use of our proprietary heat stabilization platform technology, known as ThermoVax®. To date, this business segment has been supported with government grant and contract funding from the National Institute of Allergy and Infectious Diseases (NIAID), the Defense Threat Reduction Agency (DTRA) and the Biomedical Advanced Research and Development Authority (BARDA).

For further information regarding Soligenix, Inc., please visit the Company's website at https://www.soligenix.com and follow us on LinkedIn and Twitter at @Soligenix_Inc.

This press release may contain forward-looking statements that reflect Soligenix's current expectations about its future results, performance, prospects and opportunities, including but not limited to, potential market sizes, patient populations, clinical trial enrollment, the expected timing for closing the offering described herein and the intended use of proceeds therefrom. Statements that are not historical facts, such as "anticipates," "estimates," "believes," "hopes," "intends," "plans," "expects," "goal," "may," "suggest," "will," "potential," or similar expressions, are forward-looking statements. These statements are subject to a number of risks, uncertainties and other factors that could cause actual events or results in future periods to differ materially from what is expressed in, or implied by, these statements, and include the expected amount and use of proceeds from the offering and the expected closing date of the offering. Soligenix cannot assure you that it will be able to successfully develop, achieve regulatory approval for or commercialize products based on its technologies, particularly in light of the significant uncertainty inherent in developing therapeutics and vaccines against bioterror threats, conducting preclinical and clinical trials of therapeutics and vaccines, obtaining regulatory approvals and manufacturing therapeutics and vaccines, that product development and commercialization efforts will not be reduced or discontinued due to difficulties or delays in clinical trials or due to lack of progress or positive results from research and development efforts, that it will be able to successfully obtain any further funding to support product development and commercialization efforts, including grants and awards, maintain its existing grants which are subject to performance requirements, enter into any biodefense procurement contracts with the U.S. Government or other countries, that it will be able to compete with larger and better financed competitors in the biotechnology industry, that changes in health care practice, third party reimbursement limitations and Federal and/or state health care reform initiatives will not negatively affect its business, or that the U.S. Congress may not pass any legislation that would provide additional funding for the Project BioShield program. In addition, there can be no assurance as to the timing or success of any of its clinical/preclinical trials. Despite the statistically significant result achieved in the first HyBryte (SGX301) Phase 3 clinical trial for the treatment of cutaneous T-cell lymphoma, there can be no assurance that the second HyBryte (SGX301) Phase 3 clinical trial will be successful or that a marketing authorization from the FDA or EMA will be granted. Additionally, although the EMA has agreed to the key design components of the second HyBryte(SGX301) Phase 3 clinical trial, no assurance can be given that the Company will be able to modify the development path to adequately address the FDA's concerns or that the FDA will not require a longer duration comparative study. Notwithstanding the result in the first HyBryte (SGX301) Phase 3 clinical trial for the treatment of cutaneous T-cell lymphoma and the Phase 2a clinical trial of SGX302 for the treatment of psoriasis, there can be no assurance as to the timing or success of the clinical trials of SGX302 for the treatment of psoriasis. Further, there can be no assurance that RiVax® will qualify for a biodefense Priority Review Voucher (PRV) or that the prior sales of PRVs will be indicative of any potential sales price for a PRV for RiVax®. Also, no assurance can be provided that the Company will receive or continue to receive non-dilutive government funding from grants and contracts that have been or may be awarded or for which the Company will apply in the future. These and other risk factors are described from time to time in filings with the Securities and Exchange Commission (the "SEC"), including, but not limited to, Soligenix's reports on Forms 10-Q and 10-K. Unless required by law, Soligenix assumes no obligation to update or revise any forward-looking statements as a result of new information or future events.

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/soligenix-announces-reverse-stock-split-302160182.html

SOURCE SOLIGENIX, INC.

FAQ

What is the date for Soligenix's reverse stock split?

The reverse stock split will be effective at 4:00 p.m. on June 5, 2024.

What is the new share ratio after Soligenix's reverse stock split?

The reverse stock split will convert every 16 shares into 1 share.

When will Soligenix start trading on a split-adjusted basis?

Trading on a split-adjusted basis will begin on June 6, 2024.

How does the reverse stock split affect the number of Soligenix shares?

The reverse stock split will reduce the number of outstanding shares to approximately 987,490 shares from about 15.8 million.

Will Soligenix's stockholders need new stock certificates after the reverse split?

No, stockholders holding certificated shares do not need to exchange their stock certificates.

What is the new CUSIP number for Soligenix's common stock post-reverse split?

The new CUSIP number is 834224 604.

Soligenix, Inc.

NASDAQ:SNGX

SNGX Rankings

SNGX Latest News

SNGX Stock Data

8.10M
2.51M
0.03%
5.45%
5.89%
Biotechnology
Pharmaceutical Preparations
Link
United States of America
PRINCETON