Psyence Biomedical Ltd. Announces Receipt of Staff Delisting Determination from Nasdaq
Psyence Biomedical (Nasdaq: PBM) has received a staff determination letter from Nasdaq on September 12, 2024, indicating the company's failure to regain compliance with two listing requirements by the September 9, 2024 deadline. The requirements in question are the Market Value of Listed Securities (MVLS) of $50 million and the Market Value of Publicly Held Shares (MVPHS) of $15 million for continued listing on The Nasdaq Global Market.
The company was initially notified of these deficiencies on March 11, 2024, and given 180 calendar days to comply. Facing potential suspension or delisting, Psyence Biomedical intends to request a hearing before the Nasdaq Hearings Panel, which will automatically stay any delisting action pending the hearing and any additional extension period granted by the Panel.
Psyence Biomedical (Nasdaq: PBM) ha ricevuto una lettera di determinazione dallo staff di Nasdaq il 12 settembre 2024, che indica il mancato ripristino della conformità con due requisiti di quotazione entro la scadenza del 9 settembre 2024. I requisiti in questione sono il Valore di Mercato dei Titoli Quotati (MVLS) di 50 milioni di dollari e il Valore di Mercato delle Azioni di Pubblico Possesso (MVPHS) di 15 milioni di dollari per la continua quotazione sul Nasdaq Global Market.
La società era stata inizialmente avvisata di queste carenze l'11 marzo 2024 e le sono stati concessi 180 giorni di calendario per adeguarsi. Di fronte a una possibile sospensione o delisting, Psyence Biomedical intende richiedere un'udienza davanti al Nasdaq Hearings Panel, che sospenderà automaticamente qualsiasi azione di delisting in attesa dell'udienza e di un'eventuale ulteriore estensione concessa dal Panel.
Psyence Biomedical (Nasdaq: PBM) ha recibido una carta de determinación del personal de Nasdaq el 12 de septiembre de 2024, indicando el incumplimiento de la empresa con dos requisitos de cotización antes de la fecha límite del 9 de septiembre de 2024. Los requisitos en cuestión son el Valor de Mercado de los Valores Cotizados (MVLS) de 50 millones de dólares y el Valor de Mercado de las Acciones en Circulación (MVPHS) de 15 millones de dólares para mantener la cotización en el Nasdaq Global Market.
La compañía fue inicialmente notificada de estas deficiencias el 11 de marzo de 2024 y se le otorgaron 180 días calendario para cumplir. Ante la posible suspensión o deslistado, Psyence Biomedical tiene la intención de solicitar una audiencia ante el Nasdaq Hearings Panel, que suspenderá automáticamente cualquier acción de deslistado mientras se espera la audiencia y cualquier período de extensión adicional concedido por el Panel.
Psyence Biomedical (Nasdaq: PBM)는 2024년 9월 12일 Nasdaq의 직원 결정 통지를 받았으며, 이는 회사가 2024년 9월 9일 마감일까지 두 가지 상장 요구 사항을 준수하지 못했음을 나타냅니다. 문제의 요구 사항은 상장 증권의 시장 가치 (MVLS)가 5000만 달러와 공유주식의 시장 가치 (MVPHS)가 1500만 달러로 Nasdaq Global Market에 계속 상장되기 위한 것입니다.
회사는 2024년 3월 11일 이러한 결함에 대한 초기 통지를 받았으며, 준수를 위해 180일의 시간적 여유가 주어졌습니다. 잠재적인 정지 또는 상장 폐지에 직면하여 Psyence Biomedical은 Nasdaq Hearings Panel 앞에서 청문회를 요청할 계획이며, 이 청문회가 진행되는 동안 자동으로 상장 폐지 조치를 보류하고 패널이 부여하는 추가 연장 기간도 기다릴 것입니다.
Psyence Biomedical (Nasdaq: PBM) a reçu une lettre de détermination du personnel de Nasdaq le 12 septembre 2024, indiquant l'incapacité de l'entreprise à se conformer à deux exigences de cotation avant la date limite du 9 septembre 2024. Les exigences en question sont la Valeur Marchande des Titres Cotés (MVLS) de 50 millions de dollars et la Valeur Marchande des Actions Publiquement Détentionnées (MVPHS) de 15 millions de dollars pour le maintien de la cotation sur le Nasdaq Global Market.
L'entreprise avait été initialement informée de ces lacunes le 11 mars 2024 et avait reçu 180 jours calendaires pour s'y conformer. Face à une éventuelle suspension ou radiation, Psyence Biomedical prévoit de demander une audience devant le Nasdaq Hearings Panel, qui suspendra automatiquement toute action de radiation en attendant l'audience et toute période d'extension supplémentaire accordée par le Panel.
Psyence Biomedical (Nasdaq: PBM) hat am 12. September 2024 einen Bescheid vom Nasdaq-Personal erhalten, der auf das Versagen des Unternehmens hinweist, die Einhaltung von zwei Zulassungsanforderungen bis zur Frist am 9. September 2024 wiederherzustellen. Die betreffenden Anforderungen sind der Marktwert der gelisteten Wertpapiere (MVLS) von 50 Millionen Dollar und der Marktwert der öffentlich gehaltenen Aktien (MVPHS) von 15 Millionen Dollar für die Fortführung der Notierung am Nasdaq Global Market.
Das Unternehmen wurde zunächst am 11. März 2024 über diese Mängel informiert und erhielt 180 Kalendertage zur Einhaltung. Angesichts einer möglichen Aussetzung oder Delistierung beabsichtigt Psyence Biomedical, eine Anhörung vor dem Nasdaq Hearings Panel zu beantragen, das automatisch jede Delistierungsmaßnahme bis zur Anhörung und jede zusätzliche Verlängerung, die vom Panel gewährt wird, aussetzen wird.
- None.
- Failed to meet Nasdaq's MVLS requirement of $50 million
- Failed to meet Nasdaq's MVPHS requirement of $15 million
- Facing potential suspension or delisting from Nasdaq Global Market
- Company's market value has been below requirements for over 6 months
Insights
This delisting notice from Nasdaq is a significant red flag for Psyence Biomedical. The company's failure to meet both the Market Value of Listed Securities (MVLS) and Market Value of Publicly Held Shares (MVPHS) requirements indicates severe undervaluation and potential liquidity issues. With MVLS below
The receipt of a staff delisting determination from Nasdaq presents significant legal and compliance challenges for Psyence Biomedical. The company now enters a critical phase where it must navigate the appeals process before the Hearings Panel. This process typically involves:
- Presenting a viable plan to regain compliance
- Demonstrating financial stability and growth potential
- Potentially considering alternative options such as a reverse stock split or transfer to a lower-tier market
The automatic stay on delisting action during the appeal provides a temporary reprieve, but the company must act swiftly and decisively. Failure to convince the Panel could result in delisting, potentially triggering breach of covenant issues in existing financial agreements and complicating future fundraising efforts. Shareholders should be prepared for potential dilution if the company pursues equity-based solutions to boost its market value.
NEW YORK, Sept. 13, 2024 (GLOBE NEWSWIRE) -- Psyence Biomedical Ltd. (the “Company”) (Nasdaq: PBM) announced that on September 12, 2024, the Company received a staff determination letter (the “Determination Letter”) from the Listing Qualifications Department of The Nasdaq Stock Market LLC (“Nasdaq”) notifying the Company that it had not regained compliance with the Market Value of Listed Securities (“MVLS”) Requirement and the Market Value of Publicly Held Shares (“MVPHS”) requirement by September 9, 2024.
As previously reported in a Current Report on Form 6-K filed on March 15, 2024, the Company received two deficiency letters from the Nasdaq Staff on March 11, 2024, one notifying the Company that for the last 30 consecutive business days, the Company’s MVLS was below the minimum of
As described in the Determination Letter, unless the Company timely requests a hearing before a Hearings Panel (the “Panel”), the Company’s securities would be subject to suspension/delisting. Accordingly, the Company intends to timely request a hearing before the Panel. The hearing request will automatically stay any suspension or delisting action pending the hearing and the expiration of any additional extension period granted by the Panel following the hearing.
About Psyence Biomed
Psyence Biomedical Ltd. (Nasdaq: PBM) is the world’s first life science biotechnology company focused on the development of botanical (nature-derived and non-synthetic) psilocybin-based psychedelic medicine to be listed on Nasdaq. The name “Psyence” combines the words “psychedelics” and “science” to affirm Psyence Biomed’s commitment to an evidence-based approach to innovation as it works to develop safe and effective, nature-derived psychedelic therapeutics to treat a broad range of mental health disorders. Psyence is initially focused on mental health disorders in the context of Palliative Care.
Learn more at www.psyencebiomed.com and on LinkedIn.
Contact Information
Email: ir@psyencebiomed.com
Media Inquiries: media@psyencebiomed.com
General Information: info@psyencebiomed.com
Phone: +1 416-477-1708
Investor Contact:
Jeremy Feffer
Managing Director
LifeSci Advisors
jfeffer@lifesciadvisors.com
Forward Looking Statements
This communication contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements include, but are not limited to, statements about future financial and operating results, our plans, objectives, expectations and intentions with respect to future operations, products and services; and other statements identified by words such as "will likely result," "are expected to," "will continue," "is anticipated," "estimated," "believe," "intend," "plan," "projection," "outlook" or words of similar meaning.
Forward-looking statements in this communication include statements regarding the suspension/delisting of the Company's securities and the Company's ability to regain compliance. These forward-looking statements are based on a number of assumptions, including the assumptions that the Company will secure a hearing before a Hearing Panel.
There are numerous risks and uncertainties that may cause actual results or performance to be materially different from those expressed or implied by these forward-looking statements. These risks and uncertainties include, among others: (i) the ability of Psyence Biomed to maintain the listing of its common shares and warrants on Nasdaq; and (ii) volatility in the price of the securities of Psyence Biomed due to a variety of factors, including changes in the competitive and highly regulated industries in which Psyence Biomed operates, variations in performance across competitors, changes in laws and regulations affecting Psyence Biomed’s business and changes in Psyence Biomed’s capital structure. The foregoing list of factors is not exhaustive. You should carefully consider the foregoing factors and the other risks and uncertainties described in the "Risk Factors" section of the prospectus filed by the Company with the SEC on August 30, 2024 and other documents filed by the Company from time to time with the SEC. These filings identify and address other important risks and uncertainties that could cause actual events and results to differ materially from those contained in the forward-looking statements. Actual results and future events could differ materially from those anticipated in such information. Nothing in this communication should be regarded as a representation by any person that the forward-looking statements set forth herein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved. You should not place undue reliance on forward-looking statements, which speak only as of the date they are made. Except as required by law, the Company does not intend to update these forward-looking statements.
The Company makes no medical, treatment or health benefit claims about the Company’s proposed products. The U.S. Food and Drug Administration, Health Canada or other similar regulatory authorities have not evaluated claims regarding psilocybin, psilocybin analogues, or other psychedelic compounds or nutraceutical products. The efficacy of such products has not been confirmed by approved research. There is no assurance that the use of psilocybin, psilocybin analogues, or other psychedelic compounds or nutraceuticals can diagnose, treat, cure or prevent any disease or condition. Vigorous scientific research and clinical trials are needed. The Company has not conducted clinical trials for the use of its proposed products. Any references to quality, consistency, efficacy, and safety of potential products do not imply that the Company verified such in clinical trials or that the Company will complete such trials. If the Company cannot obtain the approvals or research necessary to commercialize its business, it may have a material adverse effect on the Company’s performance and operations.
FAQ
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