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Vaccitech Announces Late-Breaker Abstract Accepted for Presentation at AASLD - The Liver Meeting® Providing Update on the Phase 1b/2a Study of VTP-300
Vaccitech plc
Wed, November 2, 2022 at 11:00 PM·3 min read
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Vaccitech plc
Vaccitech plc
OXFORD, United Kingdom, Nov. 02, 2022 (GLOBE NEWSWIRE) -- Vaccitech plc (NASDAQ: VACC), a clinical-stage biopharmaceutical company engaged in the discovery and development of novel immunotherapeutics and vaccines, today announced that the Company will be presenting an update on its Phase 1b/2a study of VTP-300, Vaccitech’s novel immunotherapy for chronic hepatitis B, at the American Association for the Study of Liver Disease (AASLD) - The Liver Meeting®, in Washington, D.C., November 4 – 8, 2022.
Poster Presentation Details:
Title:
Phase 1b/2a Study of Heterologous ChAdOx1-HBV/MVA-HBV Therapeutic Vaccination (VTP-300) Combined with Low-Dose Nivolumab (LDN) in Virally-Suppressed Patients with CHB on Nucleos(t)ide Analogues
Abstract Number:
38918
Final Poster Number:
5026
Presenter:
Dr. Young-Suk Lim, Professor of Gastroenterology in the Liver Center at University of Ulsan College of Medicine and clinical trial investigator for Vaccitech
Time/Date:
1:00 p.m. – 2:00 p.m. EST on Monday, November 7, 2022
In addition, Chief Scientific Officer, Dr. Thomas G. Evans, Vice President, Corporate Development, Nick Fullenkamp and Director, Programme Management, Dr. Henrik Sorensen will also be attending AASLD – The Liver Meeting®.
Event:
Study of Liver Disease (AASLD) - The Liver Meeting®, Washington, D.C.
Date:
Friday, November 4 – Tuesday, November 8
Attending:
Dr. Thomas G. Evans, Nick Fullenkamp, Dr. Henrik Sorensen
Available to participate in 1x1 partnering meetings
About VTP-300
VTP-300 is a novel immunotherapy, dosed in a prime-boost regimen, whereby the immune system is primed with an adenovirus (ChAdOx) and boosted with a pox virus (MVA). Both vectors have been modified to improve safety, enhance the immune response they induce and include HBV specific antigens including core, polymerase and surface antigen. Clinical data generated to date has demonstrated this regimen to be generally safe and well-tolerated, that antigen specific T cell responses are stimulated to each antigen and there were meaningful and durable reductions in hepatitis B surface antigen when this regimen is given alone or when given in combination with a low dose of nivolumab at the boost. |
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