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Allarity Therapeutics Regains Compliance with NASDAQ Minimum Bid Price Requirement

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Allarity Therapeutics, Inc. (NASDAQ: ALLR), a clinical-stage pharmaceutical company, regained compliance with Nasdaq's minimum bid price requirement, maintaining a closing bid price above $1.00 per share for over ten consecutive trading days. CEO Thomas Jensen expressed optimism about the clinical potential of their lead asset in advanced ovarian cancer and their commitment to developing new treatment options.

Allarity Therapeutics, Inc. (NASDAQ: ALLR), un'azienda farmaceutica in fase clinica, ha riacquistato la conformità con il requisito minimo di prezzo di offerta di Nasdaq, mantenendo un prezzo di offerta di chiusura superiore a $1,00 per azione per più di dieci giorni di negoziazione consecutivi. L'amministratore delegato Thomas Jensen si è espresso ottimisticamente sul potenziale clinico del loro principale asset contro il cancro ovarico avanzato e sul loro impegno nello sviluppo di nuove opzioni di trattamento.
Allarity Therapeutics, Inc. (NASDAQ: ALLR), una compañía farmacéutica en fase clínica, recuperó el cumplimiento con el requisito de precio mínimo de oferta de Nasdaq, manteniendo un precio de oferta de cierre superior a $1.00 por acción durante más de diez días consecutivos de negociación. El CEO Thomas Jensen expresó optimismo sobre el potencial clínico de su activo principal en cáncer de ovario avanzado y su compromiso en el desarrollo de nuevas opciones de tratamiento.
Allarity Therapeutics, Inc. (NASDAQ: ALLR)는 임상 단계 제약사로, 나스닥의 최소 입찰 가격 요건을 다시 충족하여 10일 연속 거래일 동안 주당 $1.00 이상의 종가를 유지했습니다. CEO 토마스 젠슨은 고급 난소암에 대한 그들의 주요 자산의 임상적 잠재력과 새로운 치료 옵션 개발에 대한 그들의 헌신에 대해 낙관적으로 언급했습니다.
Allarity Therapeutics, Inc. (NASDAQ: ALLR), une entreprise pharmaceutique en phase clinique, a retrouvé la conformité avec l'exigence de prix d'offre minimum de Nasdaq, en maintenant un prix d'offre de clôture supérieur à 1,00 $ par action pendant plus de dix jours de bourse consécutifs. Le PDG Thomas Jensen s'est montré optimiste quant au potentiel clinique de leur principal actif contre le cancer avancé de l'ovaire et leur engagement à développer de nouvelles options de traitement.
Allarity Therapeutics, Inc. (NASDAQ: ALLR), ein pharmazeutisches Unternehmen in der klinischen Phase, hat die Einhaltung der minimalen Gebotspreisanforderung von Nasdaq wieder erlangt, indem es einen Schlussgebotspreis von über 1,00 $ pro Aktie für mehr als zehn aufeinanderfolgende Handelstage beibehielt. CEO Thomas Jensen äußerte sich optimistisch über das klinische Potenzial ihrer Hauptressource bei fortgeschrittenem Eierstockkrebs und ihr Engagement für die Entwicklung neuer Behandlungsoptionen.
Positive
  • Allarity Therapeutics regained compliance with Nasdaq's minimum bid price requirement, showcasing financial stability.

  • CEO Thomas Jensen expressed optimism about the clinical potential of their lead asset in advanced ovarian cancer, highlighting promising early data.

  • The company is focused on dedicating resources to developing stenoparib and addressing the urgent needs of advanced ovarian cancer patients.

Negative
  • None.

Boston (April 29, 2024) — Allarity Therapeutics, Inc. (“Allarity” or the “Company”) (NASDAQ: ALLR), a clinical-stage pharmaceutical company dedicated to developing personalized cancer treatments, today announced that on April 27, 2024, it received formal notice from The Nasdaq Stock Market, LLC’s Office of General Counsel (“Nasdaq”). This notice confirmed that the Company has regained compliance with the minimum bid price requirement as set forth in Nasdaq’s Listing Rule 5550(a)(2) (the “Bid Price Rule”). Nasdaq noted that since April 9, 2024, Allarity’s stock has maintained a closing bid price above $1.00 per share for more than ten consecutive trading days, thereby meeting the requirements for regaining compliance.

Thomas Jensen, CEO of Allarity Therapeutics, stated, "We are very pleased to announce NASDAQ’s confirmation of our compliance with the minimum bid price requirement. Looking at the bigger picture, we are filled with optimism about the clinical potential of our lead asset in the area of advanced ovarian cancer, given the very promising early data that we have received from our ongoing phase 2 stenoparib trial. I am also very optimistic about demonstrating full compliance with the Nasdaq Listing Rule 5550(b)(1) which requires a minimum stockholders’ equity on a timely basis. Most importantly, we expect to continue to dedicate all our resources to the continued development of stenoparib, aiming to change lives by addressing the urgent needs of advanced ovarian cancer patients who urgently require new and better treatment options.”

About Allarity Therapeutics
Allarity Therapeutics, Inc. (NASDAQ: ALLR) is a clinical-stage biopharmaceutical company dedicated to developing personalized cancer treatments. The Company is focused on development of stenoparib, a novel PARP/Tankyrase inhibitor for advanced ovarian cancer patients, using its DRP® companion diagnostic for patient selection in the ongoing phase 2 clinical trial, NCT03878849. Allarity is headquartered in the U.S., with a research facility in Denmark, and is committed to addressing significant unmet medical needs in cancer treatment. For more information, visit www.allarity.com.

Follow Allarity on Social Media
LinkedIn: https://www.linkedin.com/company/allaritytx/
X: https://twitter.com/allaritytx

Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements provide the Company’s current expectations or forecasts of future events. The words “anticipates,” “believe,” “continue,” “could,” “estimate,” “expect,” “intends,” “may,” “might,” “plan,” “possible,” “potential,” “predicts,” “project,” “should,” “would” and similar expressions may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. These forward-looking statements include, but are not limited to, statements relating to regaining compliance with Nasdaq’s continued listing requirements, the timing and effect thereof, reducing operating expenses, converting debt and raising additional capital and the effectiveness of the Company’s DRP® companion diagnostics platform in predicting whether a particular patient is likely to respond to a specific drug. Any forward-looking statements in this press release are based on management’s current expectations of future events and are subject to multiple risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to, the risk that the Company is not able to effect a reverse stock split, reduce operating expenses, convert debt and raise additional capital. For a discussion of other risks and uncertainties, and other important factors, any of which could cause our actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in our Form S-1 registration statement filed on October 30, 2023, as amended and our Form 10-K annual report on file with the Securities and Exchange Commission (the “SEC”), available at the SEC’s website at www.sec.gov, and as well as discussions of potential risks, uncertainties and other important factors in the Company’s subsequent filings with the SEC. All information in this press release is as of the date of the release, and the Company undertakes no duty to update this information unless required by law.

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Company Contact:         
        investorrelations@allarity.com
     
Media Contact:
        Thomas Pedersen
        Carrotize PR & Communications
        +45 6062 9390
        tsp@carrotize.com

 

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Allarity Therapeutics, Inc.

NASDAQ:ALLR

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2.03M
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Research and Development in Biotechnology
Professional, Scientific, and Technical Services
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United States of America
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About ALLR

oncology venture is a drug development company formed in 2012 dedicated to unlock the potential of new oncology products, and rescue failed drugs. our method improves the efficacy of the drugs, increase the response rate in cancer patients, reduce timelines and improve success rates in oncology drug development.