Outlook Therapeutics® Announces Effective Date for 1-for-20 Reverse Stock Split
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Insights
The announcement of a 1-for-20 reverse stock split by Outlook Therapeutics is a strategic move aimed at addressing the Nasdaq's minimum bid price requirement. This is often seen as a remedial step for companies facing delisting risks due to their stock trading below a certain threshold. The immediate effect on the stock market is typically a perceived stabilization of the stock price, as the reduced number of shares outstanding can lead to a higher price per share, albeit without changing the company's market capitalization.
However, the long-term impact on the stock's performance is contingent on the company's fundamental performance. Investors should monitor the progress towards FDA approval for the company's ophthalmic formulation, as this will be a critical driver of value. The reverse stock split does not inherently add value to the company but can sometimes be viewed negatively by the market as it may suggest that the company has been unable to organically maintain its stock price above the required threshold.
Reverse stock splits are often employed by companies to avoid delisting and to make their stock more attractive to institutional investors, who may be prohibited from investing in stocks below a certain price. From a market research perspective, the reduction in outstanding shares from approximately 260.3 million to 13.0 million will significantly decrease the liquidity of the stock, which can lead to higher volatility. Additionally, the perception of the company's future prospects can be influenced by such corporate actions.
It is crucial to assess the market's reception of the reverse stock split in the following trading sessions. A successful stabilization or increase in the stock price can provide the company with better financing opportunities, which is essential for a biopharmaceutical firm in the development stage. However, if the market reacts negatively, it could lead to a decline in investor confidence, potentially impacting future capital raising efforts.
In the biopharmaceutical sector, the pursuit of FDA approval is a rigorous and costly process, often necessitating substantial capital. Outlook Therapeutics' strategy to implement a reverse stock split indicates a focus on maintaining its listing status, which is crucial for access to capital markets. The company's progress towards FDA approval for its ophthalmic formulation of bevacizumab is a pivotal factor that will determine its financial health and ability to attract investment.
For stakeholders, the critical aspect to consider is the company's clinical and regulatory pathway following the reverse stock split. The success of their lead product candidate can significantly influence the company's valuation and its ability to attract partnerships or funding. Stakeholders should be attentive to the company's forthcoming announcements on clinical trial results and regulatory interactions, as these will provide insights into the company's operational trajectory post-reverse stock split.
ISELIN, N.J., March 12, 2024 (GLOBE NEWSWIRE) -- Outlook Therapeutics, Inc. (Nasdaq: OTLK) (the “Company”), a biopharmaceutical company working to achieve FDA approval for the first ophthalmic formulation of bevacizumab for the treatment of retinal diseases, today announced that a 1-for-20 reverse stock split of its outstanding shares of common stock will be effective on March 14, 2024.
The Company’s common stock will begin trading on a reverse stock split-adjusted basis at the opening of the market on March 14, 2024. Following the reverse stock split, the Company’s common stock will continue to trade on The Nasdaq Capital Market under the symbol “OTLK” with the new CUSIP number 69012T 305. The reverse stock split is part of the Company’s plan to regain compliance with the minimum bid price requirement for continued listing on The Nasdaq Capital Market.
At the effective time of the reverse split, every 20 issued and outstanding shares of the Company’s common stock will automatically be combined into one issued and outstanding share of the Company’s common stock without any change in the par value per share. Fractional shares will not be issued in connection with the reverse stock split. Stockholders who would otherwise be entitled to receive a fractional share will be entitled to receive a cash payment. The reverse stock split will affect all stockholders uniformly and will not alter any stockholder’s relative interest in the Company’s equity securities, except for any adjustments for fractional shares. The number of authorized shares of the Company’s common stock will be proportionately reduced at the same ratio as the reverse stock split, for a total of 60,000,000 authorized shares of common stock following the reverse split. In addition, proportionate adjustments will be made to the number of shares underlying, and the exercise or conversion prices of, the Company’s outstanding stock options, and to the number of shares of common stock issuable under the Company’s equity incentive plans.
The reverse stock split will reduce the number of issued and outstanding shares of the Company’s common stock from approximately 260.3 million to approximately 13.0 million.
About Outlook Therapeutics, Inc.
Outlook Therapeutics is a biopharmaceutical company working to achieve FDA approval for the launch of ONS-5010/ LYTENAVA™ (bevacizumab-vikg) as the first FDA-approved ophthalmic formulation of bevacizumab for use in retinal indications, including wet AMD, DME and BRVO. If ONS-5010 ophthalmic bevacizumab is approved, Outlook Therapeutics expects to commercialize it as the first and only FDA-approved ophthalmic formulation of bevacizumab for use in treating retinal diseases in the United States, United Kingdom, Europe, Japan, and other markets. As part of Outlook Therapeutics' multi-year commercial planning process, Outlook Therapeutics and Cencora entered into a strategic commercialization agreement to expand Outlook Therapeutics’ reach for connecting to retina specialists and their patients. Cencora will provide third-party logistics (3PL) services and distribution, as well as pharmacovigilance services and other services in the United States. For more information, please visit www.outlooktherapeutics.com.
Forward-Looking Statements
This press release contains forward-looking statements. All statements other than statements of historical facts are “forward-looking statements,” including those relating to future events. In some cases, you can identify forward-looking statements by terminology such as “expect,” “plan,” “will,” or “would” the negative of terms like these or other comparable terminology, and other words or terms of similar meaning. These include, among others, statements about the reverse stock split and the timing thereof, the impact of the reverse stock split on stockholders, including any adjustments that may result from the treatment of fractional shares, and option holders, the potential impact of the reverse stock split on the bid price of the Company’s common stock, the potential for the Company to regain compliance with the minimum bid price requirement for continued listing on The Nasdaq Capital Market, the expected number of shares of common stock to be issued and outstanding following the reverse stock split, ONS-5010’s potential as the first FDA-approved ophthalmic formulation of bevacizumab for use in retinal indications, including wet AMD, DME and BRVO, expectations concerning decisions of the FDA, plans for potential commercial launch of ONS-5010, expectations concerning the relationship with Cencora and the benefits and potential expansion thereof, and other statements that are not historical fact. Although Outlook Therapeutics believes that it has a reasonable basis for the forward-looking statements contained herein, they are based on current expectations about future events affecting Outlook Therapeutics and are subject to risks, uncertainties and factors relating to its operations and business environment, all of which are difficult to predict and many of which are beyond its control. These risk factors include those risks associated with developing pharmaceutical product candidates, risks of conducting clinical trials and risks in obtaining necessary regulatory approvals, the content and timing of decisions by the FDA, as well as those risks detailed in Outlook Therapeutics’ filings with the Securities and Exchange Commission (the SEC), including the Annual Report on Form 10-K for the fiscal year ended September 30, 2023, filed with the SEC on December 22, 2023, and future quarterly reports Outlook Therapeutics files with the SEC, which include uncertainty of market conditions and future impacts related to macroeconomic factors, including as a result of the ongoing overseas conflict, high interest rates, inflation and potential future bank failures on the global business environment. These risks may cause actual results to differ materially from those expressed or implied by forward-looking statements in this press release. All forward-looking statements included in this press release are expressly qualified in their entirety by the foregoing cautionary statements. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. Outlook Therapeutics does not undertake any obligation to update, amend or clarify these forward-looking statements whether as a result of new information, future events or otherwise, except as may be required under applicable securities law.
Investor Inquiries:
Jenene Thomas
Chief Executive Officer
JTC Team, LLC
T: 833.475.8247
OTLK@jtcir.com
FAQ
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