Aptose Biosciences receives extension from Nasdaq to comply with listing requirements by March 31, 2025, following recent funding and clinical agreements.
Quiver AI Summary
Aptose Biosciences Inc. has received an extension from the Nasdaq Hearings Panel to demonstrate compliance with listing requirements for The Nasdaq Stock Market, specifically needing to show at least $2.5 million in shareholders' equity and a minimum bid price of $1.00 per share by March 31, 2025. The company's recent activities include closing an $8 million public offering and entering a clinical development agreement with the National Cancer Institute for its lead drug, tuspetinib, aimed at treating acute myeloid leukemia and myelodysplastic syndromes. Aptose, focused on developing precision oncology treatments, has seen promising data in clinical presentations regarding tuspetinib’s efficacy in newly diagnosed AML patients.
Potential Positives
- The Nasdaq Hearings Panel granted Aptose an extension to demonstrate compliance with listing criteria, providing the company with additional time to achieve necessary financial benchmarks.
- Aptose successfully closed an $8 million public offering, enhancing its financial position and stability during a critical period.
- The company signed a clinical development agreement with the National Cancer Institute, validating its lead drug tuspetinib and potentially accelerating its development and credibility in the oncology field.
- Clinical data supporting tuspetinib's efficacy was presented at a prestigious conference, indicating strong prospects for the drug's performance in treating newly diagnosed acute myeloid leukemia patients.
Potential Negatives
- The company's compliance with NASDAQ Listing Rules is uncertain, requiring proof of minimum shareholders' equity and stock price by March 31, 2025, which could jeopardize its listing.
- The requirement to maintain a stock price of at least $1.00 for a minimum of 10 consecutive business days highlights significant investor confidence issues.
FAQ
What recent decision did the Nasdaq Hearings Panel make regarding Aptose Biosciences?
The Nasdaq Hearings Panel granted Aptose an extension to demonstrate compliance with listing criteria by March 31, 2025.
What are Aptose's compliance requirements for Nasdaq?
Aptose must have a minimum of $2.5 million in shareholders’ equity and meet a minimum bid price of $1.00 per share.
What clinical developments has Aptose announced recently?
Aptose announced an $8 million public offering and a clinical development agreement with the National Cancer Institute for tuspetinib.
What is tuspetinib and its significance in Aptose's pipeline?
Tuspetinib is Aptose's lead oral kinase inhibitor, showing promise as a treatment for acute myeloid leukemia in recent clinical trials.
How does Aptose intend to enhance its oncology therapeutics?
Aptose aims to develop targeted agents that provide single-agent efficacy and boost the effectiveness of other cancer therapies.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$APTO Insider Trading Activity
$APTO insiders have traded $APTO stock on the open market 1 times in the past 6 months. Of those trades, 1 have been purchases and 0 have been sales.
Here’s a breakdown of recent trading of $APTO stock by insiders over the last 6 months:
- WILLIAM G. RICE (Chair, President & CEO) purchased 100,000 shares.
To track insider transactions, check out Quiver Quantitative's insider trading dashboard.
$APTO Hedge Fund Activity
We have seen 8 institutional investors add shares of $APTO stock to their portfolio, and 8 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- ARMISTICE CAPITAL, LLC added 175,000 shares (+10.2%) to their portfolio in Q3 2024
- SIGMA PLANNING CORP added 167,282 shares (+71.3%) to their portfolio in Q3 2024
- UBS GROUP AG added 133,476 shares (+inf%) to their portfolio in Q3 2024
- TWO SIGMA SECURITIES, LLC added 30,427 shares (+inf%) to their portfolio in Q3 2024
- ANNANDALE CAPITAL, LLC added 26,666 shares (+inf%) to their portfolio in Q3 2024
- CITADEL ADVISORS LLC removed 25,691 shares (-100.0%) from their portfolio in Q2 2024
- TD WATERHOUSE CANADA INC. removed 6,661 shares (-90.7%) from their portfolio in Q3 2024
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
Full Release
SAN DIEGO and TORONTO, Dec. 19, 2024 (GLOBE NEWSWIRE) -- Aptose Biosciences Inc. (“Aptose” or the “Company”) (NASDAQ: APTO, TSX: APS), a clinical-stage precision oncology company developing highly differentiated targeted agents to treat hematologic malignancies, today announced that the Nasdaq Hearings Panel (“Panel”) has granted the Company’s request for an extension to evidence compliance with all applicable criteria for continued listing on The Nasdaq Stock Market.
On or before March 31, 2025, the Company will be required to demonstrate compliance with NASDAQ Listing Rule 5550(b)(1) requiring the Company to have a minimum of $2.5 million in shareholders’ equity (the “Equity Rule”) and NASDAQ Listing Rule 5550(a)(2) requiring the Company to have a minimum bid price of $1.00 (the “Minimum Bid Price Rule”). To evidence compliance with the Minimum Bid Price requirement, the Company’s common stock must close at or above $1.00 per share for a minimum of 10 consecutive business days by March 31, 2025.
The Nasdaq hearing on the matter was held on November 21, 2024. Since the hearing, Aptose announced the closing of an $8 million public offering, announced the signing of a prestigious clinical development agreement with the National Cancer Institute to develop the Company’s lead drug tuspetinib for acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS), and presented clinical data at the American Society of Hematology (ASH) Annual Meeting supporting tuspetinib triplet drug therapy for newly diagnosed AML patients.
About Aptose
Aptose Biosciences is a clinical-stage biotechnology company committed to developing precision medicines addressing unmet medical needs in oncology, with an initial focus on hematology. The Company's small molecule cancer therapeutics pipeline includes products designed to provide single agent efficacy and to enhance the efficacy of other anti-cancer therapies and regimens without overlapping toxicities. The Company’s lead clinical-stage, oral kinase inhibitor tuspetinib (TUS) has demonstrated activity as a monotherapy and in combination therapy in patients with relapsed or refractory acute myeloid leukemia (AML) and is being developed as a frontline triplet therapy in newly diagnosed AML. For more information, please visit www.aptose.com.
Forward Looking Statements
This press release may contain forward-looking statements within the meaning of Canadian and U.S. securities laws, including, but not limited to, statements relating to the therapeutic potential of tuspetinib, its clinical development and safety profile, as well as statements relating to the Company’s and other statements including words such as “continue”, “expect”, “intend”, “will”, “should”, “would”, “may”, and other similar expressions. Such statements reflect our current views with respect to future events and are subject to risks and uncertainties and are necessarily based upon a number of estimates and assumptions that, while considered reasonable by us are inherently subject to significant business, economic, competitive, political and social uncertainties and contingencies. Many factors could cause our actual results, performance or achievements to be materially different from any future results, performance or achievements described in this press release. Such factors could include, among others: our ability to regain compliance with the NASDAQ Listing Rules prior to March 31, 2025; our ability to obtain the capital required for research and operations and to continue as a going concern; the inherent risks in early stage drug development including demonstrating efficacy; development time/cost and the regulatory approval process; the progress of our clinical trials; our ability to find and enter into agreements with potential partners; our ability to attract and retain key personnel; changing market conditions; inability of new manufacturers to produce acceptable batches of GMP in sufficient quantities; unexpected manufacturing defects; and other risks detailed from time-to-time in our ongoing quarterly filings, annual information forms, annual reports and annual filings with Canadian securities regulators and the United States Securities and Exchange Commission.
Should one or more of these risks or uncertainties materialize, or should the assumptions set out in the section entitled "Risk Factors" in our filings with Canadian securities regulators and the United States Securities and Exchange Commission underlying those forward-looking statements prove incorrect, actual results may vary materially from those described herein. These forward-looking statements are made as of the date of this press release and we do not intend, and do not assume any obligation, to update these forward-looking statements, except as required by law. We cannot assure you that such statements will prove to be accurate as actual results and future events could differ materially from those anticipated in such statements. Investors are cautioned that forward-looking statements are not guarantees of future performance and accordingly investors are cautioned not to put undue reliance on forward-looking statements due to the inherent uncertainty therein.
For further information, please contact:
Aptose
Biosciences
Inc.
Susan Pietropaolo
Corporate Communications & Investor Relations
201-923-2049
[email protected]