BioVie Inc. Announces Closing of Registered Direct Offering
BioVie Inc (Nasdaq: BIVI) has completed its previously announced registered direct offering of 1,146,000 shares of common stock at $2.83 per share, raising gross proceeds of $3,243,180. The clinical-stage company, which develops drug therapies for liver disease and neurological disorders, plans to use the net proceeds for working capital and general corporate purposes. ThinkEquity served as the sole placement agent for the offering, which was conducted under a shelf registration statement filed with the SEC in August 2023.
BioVie Inc (Nasdaq: BIVI) ha completato la sua offerta diretta registrata precedentemente annunciata di 1.146.000 azioni di azioni ordinarie a $2,83 per azione, raccogliendo proventi lordi di $3.243.180. L'azienda in fase clinica, che sviluppa terapie farmacologiche per malattie del fegato e disturbi neurologici, prevede di utilizzare i proventi netti per il capitale circolante e scopi aziendali generali. ThinkEquity ha agito come unico agente di collocamento per l'offerta, che è stata condotta ai sensi di una dichiarazione di registrazione shelf depositata presso la SEC nell'agosto 2023.
BioVie Inc (Nasdaq: BIVI) ha completado su oferta directa registrada previamente anunciada de 1.146.000 acciones de acciones ordinarias a $2,83 por acción, recaudando ingresos brutos de $3.243.180. La empresa en etapa clínica, que desarrolla terapias farmacológicas para enfermedades del hígado y trastornos neurológicos, planea utilizar los ingresos netos para capital de trabajo y propósitos corporativos generales. ThinkEquity actuó como el único agente de colocación para la oferta, que se llevó a cabo bajo una declaración de registro tipo shelf presentada ante la SEC en agosto de 2023.
BioVie Inc (Nasdaq: BIVI)는 1,146,000주의 보통주를 주당 $2.83에 판매하는 등록된 직접 제안을 완료하였으며, 총 수익금은 $3,243,180에 달합니다. 간 질환 및 신경 질환에 대한 약물 치료 개발을 전문으로 하는 임상 단계 회사는 순수익금을 운영 자본 및 일반 기업 용도로 사용할 계획입니다. ThinkEquity는 2023년 8월 SEC에 제출된 선반 등록 신청서에 따라 진행된 이번 제안의 유일한 배치 에이전트 역할을 했습니다.
BioVie Inc (Nasdaq: BIVI) a complété son offre directe enregistrée précédemment annoncée de 1.146.000 actions ordinaires au prix de 2,83 $ par action, levant des recettes brutes de 3.243.180 $. Cette entreprise en phase clinique, qui développe des thérapies médicamenteuses pour les maladies du foie et les troubles neurologiques, prévoit d'utiliser les produits nets pour le fonds de roulement et les objectifs généraux de l'entreprise. ThinkEquity a été le seul agent de placement pour l'offre, qui a été réalisée dans le cadre d'une déclaration d'enregistrement type shelf déposée auprès de la SEC en août 2023.
BioVie Inc (Nasdaq: BIVI) hat ihr zuvor angekündigtes registriertes Direktangebot über 1.146.000 Aktien zum Preis von $2,83 pro Aktie abgeschlossen und dabei einen Bruttoerlös von $3.243.180 erzielt. Das klinische Unternehmen, das Arzneimitteltherapien für Lebererkrankungen und neurologische Störungen entwickelt, plant die Verwendung der Nettoerlöse für Betriebskapital und allgemeine Unternehmenszwecke. ThinkEquity fungierte als alleiniger Platzierungsvermittler für das Angebot, das unter einer im August 2023 bei der SEC eingereichten Shelf-Registrierungserklärung durchgeführt wurde.
- Secured $3.24 million in gross proceeds through stock offering
- Successfully completed at-market offering under Nasdaq rules
- Strengthened working capital position
- Dilution of existing shareholders' equity through new share issuance
- Stock offering priced at relatively low $2.83 per share
Insights
The
CARSON CITY, Nev., Oct. 29, 2024 (GLOBE NEWSWIRE) -- BioVie Inc. (Nasdaq: BIVI), (“BioVie” or the “Company”), a clinical-stage company developing innovative drug therapies to treat chronic debilitating conditions including liver disease and neurological and neuro-degenerative disorders, today announced the closing of its previously announced registered direct offering of 1,146,000 shares of its common stock priced at-the-market under Nasdaq rules at a price of
The gross proceeds to the Company from the offering are
ThinkEquity acted as sole placement agent for the offering.
The shares of common stock offered in the registered direct offering were offered and sold pursuant to a shelf registration statement on Form S-3 (File No. 333-274083), including a base prospectus, filed with the U.S. Securities and Exchange Commission (the “SEC”) on August 18, 2023 and declared effective on August 28, 2023. A final prospectus supplement and accompanying prospectus describing the terms of the offering was filed with the SEC and is available on its website at www.sec.gov. Copies of the final prospectus supplement and the accompanying prospectus relating to the offering may also be obtained, when available, from the offices of ThinkEquity, 17 State Street, 41st Floor, New York, New York 10004.
This press release shall not constitute an offer to sell or a solicitation of an offer to buy, nor shall there be any sale of these securities in any state or jurisdiction in which such an offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.
About BioVie Inc.
BioVie Inc. (NASDAQ: BIVI) is a clinical-stage company developing innovative drug therapies for the treatment of neurological and neurodegenerative disorders (Long COVID, Alzheimer's disease and Parkinson’s disease) and advanced liver disease. In neurodegenerative disease, the Company’s drug candidate bezisterim inhibits inflammatory activation of extracellular signal-regulated kinase and the transcription factor, Nuclear factor- kB, and the associated neuroinflammation and insulin resistance but not ERK and NFkB homeostatic functions (e.g., insulin signaling and neuron growth and survival). Both neuroinflammation and insulin resistance are drivers of AD and PD. Persistent systematic inflammation and neuroinflammation are key features in patients with neurological symptoms of Long COVID. In liver disease, the Company’s Orphan drug candidate BIV201 (continuous infusion terlipressin), with FDA Fast Track status, is being evaluated and discussed with guidance received from the FDA regarding the design of Phase 3 clinical testing of BIV201 for the reduction of further decompensation in participants with liver cirrhosis and ascites. The active agent is approved in the U.S. and in about 40 countries for related complications of advanced liver cirrhosis. For more information, visit www.bioviepharma.com.
Forward-Looking Statements
This press release contains forward-looking statements, which may be identified by words such as "expect," "look forward to," "anticipate" "intend," "plan," "believe," "seek," "estimate," "will," "project" or words of similar meaning. Although BioVie Inc. believes such forward-looking statements are based on reasonable assumptions, it can give no assurance that its expectations will be attained. Actual results may vary materially from those expressed or implied by the statements herein due to the Company's ability to successfully raise sufficient capital on reasonable terms or at all, available cash on hand and contractual and statutory limitations that could impair our ability to pay future dividends, our ability to complete our pre-clinical or clinical studies and to obtain approval for our product candidates, our ability to successfully defend potential future litigation, changes in local or national economic conditions as well as various additional risks, many of which are now unknown and generally out of the Company's control, and which are detailed from time to time in reports filed by the Company with the SEC, including quarterly reports on Form 10-Q, reports on Form 8-K and annual reports on Form 10-K. BioVie Inc. does not undertake any duty to update any statements contained herein (including any forward-looking statements), except as required by law.
For Investor Relations Inquiries:
Bruce Mackle
Managing Director, LifeSci Advisors, LLC
bmackle@lifesciadvisors.com
For Media Relations Inquiries:
Melyssa Weible
Managing Partner, Elixir Health Public Relations
mweible@elixirhealthpr.com
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