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Vir Biotechnology to Host Virtual Investor Event on PRO-XTEN™ Masked T-Cell Engager Programs

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Vir Biotechnology (NASDAQ:VIR) has announced a virtual investor event scheduled for January 8, 2025, at 5:00 a.m. PT / 8:00 a.m. ET. The event will present initial data from two Phase 1 T-cell engager programs: VIR-5818, targeting HER2-expressing solid tumors, and VIR-5500, targeting PSMA in metastatic castration-resistant prostate cancer (mCRPC). Updates on the PRO-XTEN™ platform will also be discussed. The presentation will be accessible via webcast on the company's investor relations website and archived for 30 days.

Vir Biotechnology (NASDAQ:VIR) ha annunciato un evento virtuale per gli investitori programmato per 8 gennaio 2025 alle 5:00 a.m. PT / 8:00 a.m. ET. Durante l'evento verranno presentati i dati iniziali di due programmi di fase 1 per gli engager T-cell: VIR-5818, mirato ai tumori solidi che esprimono HER2, e VIR-5500, mirato al PSMA nel cancro della prostata metastatico resistente alla castrazione (mCRPC). Saranno inoltre forniti aggiornamenti sulla piattaforma PRO-XTEN™. La presentazione sarà accessibile tramite webcast sul sito web delle relazioni con gli investitori dell'azienda e archiviata per 30 giorni.

Vir Biotechnology (NASDAQ:VIR) ha anunciado un evento virtual para inversionistas programado para el 8 de enero de 2025 a las 5:00 a.m. PT / 8:00 a.m. ET. El evento presentará datos iniciales de dos programas de enganche de células T de fase 1: VIR-5818, dirigido a tumores sólidos que expresan HER2, y VIR-5500, dirigido a PSMA en cáncer de próstata metastásico resistente a la castración (mCRPC). También se discutirán las actualizaciones sobre la plataforma PRO-XTEN™. La presentación será accesible a través de un webcast en el sitio web de relaciones con inversionistas de la compañía y se archivará durante 30 días.

Vir Biotechnology (NASDAQ:VIR)는 2025년 1월 8일 오전 5시 PT / 오전 8시 ET로 예정된 가상 투자자 이벤트를 발표했습니다. 이번 이벤트에서는 HER2를 발현하는 고형 종양을 대상으로 하는 VIR-5818와 전이성 안드로겐 저항성 전립선암(mCRPC)을 대상으로 하는 VIR-5500에 대한 1상 T세포 자극제 프로그램의 초기 데이터가 발표됩니다. 또한 PRO-XTEN™ 플랫폼에 대한 업데이트도 논의될 예정입니다. 발표 내용은 회사의 투자자 관계 웹사이트를 통해 웹캐스트로 제공되며, 30일간 아카이브됩니다.

Vir Biotechnology (NASDAQ:VIR) a annoncé un événement virtuel pour les investisseurs prévu pour le 8 janvier 2025 à 5h00 PT / 8h00 ET. L'événement présentera des données initiales de deux programmes d'engagers de cellules T de phase 1 : VIR-5818, ciblant les tumeurs solides exprimant HER2, et VIR-5500, ciblant le PSMA dans le cancer de la prostate résistant à la castration et métastatique (mCRPC). Des mises à jour sur la plateforme PRO-XTEN™ seront également discutées. La présentation sera accessible par webdiffusion sur le site Web des relations avec les investisseurs de l'entreprise et sera archivée pendant 30 jours.

Vir Biotechnology (NASDAQ:VIR) hat eine virtuelle Investorenveranstaltung für den 8. Januar 2025 um 5:00 Uhr PT / 8:00 Uhr ET angekündigt. Bei der Veranstaltung werden erste Daten aus zwei Phase-1-T-Zell-Engager-Programmen präsentiert: VIR-5818, das sich auf HER2-exprimierende solide Tumoren konzentriert, und VIR-5500, das auf PSMA bei metastasierendem kastrationsresistentem Prostatakrebs (mCRPC) abzielt. Updates zur PRO-XTEN™ Plattform werden ebenfalls erörtert. Die Präsentation wird über einen Webcast auf der Investor-Relations-Website des Unternehmens zugänglich sein und für 30 Tage archiviert.

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SAN FRANCISCO--(BUSINESS WIRE)-- Vir Biotechnology, Inc. (NASDAQ:VIR) today announced it will host a virtual investor event to discuss initial data from the dual-masked Phase 1 T-cell engagers VIR-5818 targeting a variety of HER2-expressing solid tumors and VIR-5500 targeting PSMA in metastatic castration-resistant prostate cancer (mCRPC) along with updates on the PRO-XTEN™ platform on January 8, 2025, at 5:00 a.m. PT / 8:00 a.m. ET.

A live webcast will be available on https://investors.vir.bio/ and will be archived on www.vir.bio for 30 days.

About Vir Biotechnology, Inc.

Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes infectious disease programs for chronic hepatitis delta and chronic hepatitis B infections and programs across several clinically validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of other infectious diseases and oncologic malignancies. Vir Biotechnology routinely posts information that may be important to investors on its website.

Vir Biotechnology has exclusive rights to the PRO-XTEN™ masking platform for oncology and infectious disease. PRO-XTEN™ is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as “should,” “could,” “may,” “might,” “will,” “plan,” “potential,” “aim,” “expect,” “anticipate,” “promising” and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. These forward-looking statements are based on Vir’s expectations and assumptions as of the date of this press release. Forward-looking statements contained in this press release include, but are not limited to, statements regarding Vir’s strategy and plans; Vir’s ability to realize the anticipated benefits from the exclusive worldwide license agreement with Sanofi; difficulties or unanticipated expenses in connection with the agreement, and the potential effects on Vir’s earnings; the risk that Vir’s investment in connection with the agreement will lose value for any number of reasons; the ability of the parties to initiate, progress or complete clinical studies within currently anticipated timelines or at all, and the possibility of unfavorable results from studies, including those involving VIR-5818 and VIR-5500, and any additional programs that may become subject to the agreement; the potential clinical effects, potential benefits, safety and efficacy of the investigational products that are the subject of these programs; data from ongoing studies evaluating such investigational products and programs; Vir’s ability to file applications for regulatory approval or receive regulatory approvals in a timely manner or at all for such investigational products and programs, and the risk that any such approvals may be subject to significant limitations on use; the possibility that the agreement may be terminated for any number of reasons, or that development of the investigational products and programs subject to the agreement may be discontinued, and therefore may never be successfully commercialized; Vir’s ability to successfully commercialize any approved drug products resulting from the agreement; and any assumptions underlying any of the foregoing. Many factors may cause differences between current expectations and actual results, including unexpected safety or efficacy data or results observed during clinical studies or in data readouts; the occurrence of adverse safety events; risks of unexpected costs, delays or other unexpected hurdles; difficulties in collaborating with other companies; successful development and/or commercialization of alternative product candidates by Vir’s competitors; changes in expected or existing competition; delays in or disruptions to Vir’s business or clinical studies due to geopolitical changes or other external factors; failure to achieve any necessary regulatory approvals; and unexpected litigation or other disputes. Drug development and commercialization involve a high degree of risk, and only a small number of research and development programs result in commercialization of a product. Results in early-stage clinical studies may not be indicative of full results or results from later stage or larger scale clinical studies and do not ensure regulatory approval. You should not place undue reliance on these statements, or the scientific data presented. Other factors that may cause actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in Vir’s filings with the U.S. Securities and Exchange Commission, including the section titled “Risk Factors” contained therein. Except as required by law, Vir assumes no obligation to update any forward-looking statements contained herein to reflect any change in expectations, even as new information becomes available.

Media

Arran Attridge

Senior Vice President, Corporate Communications

aattridge@vir.bio

Investors

Richard Lepke

Senior Director, Investor Relations

rlepke@vir.bio

Source: Vir Biotechnology, Inc.

FAQ

When is Vir Biotechnology's investor event for PRO-XTEN T-cell engager programs?

Vir Biotechnology's virtual investor event is scheduled for January 8, 2025, at 5:00 a.m. PT / 8:00 a.m. ET.

What clinical programs will VIR discuss during the January 2025 investor event?

VIR will discuss initial data from two Phase 1 T-cell engagers: VIR-5818 for HER2-expressing solid tumors and VIR-5500 for PSMA in metastatic castration-resistant prostate cancer (mCRPC).

How can investors access Vir Biotechnology's January 2025 virtual event?

Investors can access the event through a live webcast available on https://investors.vir.bio/, which will be archived on www.vir.bio for 30 days.

What types of cancers does VIR-5818 target?

VIR-5818 targets a variety of HER2-expressing solid tumors.

Vir Biotechnology, Inc.

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Biotechnology
Biological Products, (no Disgnostic Substances)
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United States of America
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