Vaccitech Ltd, a clinical-stage T cell immunotherapy company developing products to treat and prevent cancer and infectious diseases, reports successful recruitment and vaccination for its Universal influenza A vaccine MVA-NP+M1 (VTP-100), across two Phase 2 clinical studies, FLU009 and FLU010. Final primary endpoint data from FLU010 is expected in early 2020. The Phase 2 studies are part of a dual development pathway for VTP-100 that will address both pandemic and seasonal influenza vaccine markets.
FLU010 is a randomised, double-blind, placebo controlled, influenza challenge study conducted in Antwerp, Belgium, and co-funded by BARDA for $8.6M. There have been 145 participants vaccinated, of which 108 were challenged with the A/Belgium/4217/2015 (H3N2) influenza virus. Another group is scheduled to be challenged by the end of year. FLU010, approved by both the FDA and the Belgian Regulatory Authority, FAMHP, is designed to assess the protective capabilities of VTP-100 as a standalone influenza vaccine. The study is powered to evaluate potential correlations of vaccine-induced protection from influenza. Top-line data will read out in early 2020.
Vaccitech's wholly-owned subsidiary, Vaccitech Australia Limited Pty, also confirms that FLU009 is on track to collect a high number of influenza A positive samples from 2149 participants. The 2019 season of influenza in Australia has produced an especially high number of influenza cases and is one of the longest seasons on record. FLU009 is a single-blind, randomised, placebo-controlled Phase 2 field trial in Australia. The study will test, by examining laboratory confirmed influenza illness, the additive protective efficacy against influenza A viruses that VTP-100 provides to that of licenced seasonal influenza vaccines. An interim analysis of results, expected early 2020, will steer Vaccitech’s decision on how many participants will be recruited for a second season. It is anticipated that 3,800 participants will be the maximum number, which would give a total of 6,000 over the two influenza seasons. Approximately a quarter of the participants will be aged 65 years and over – one of the most at-risk demographic groups for influenza-related morbidity and mortality.
Bill Enright, Vaccitech Chief Executive Officer, comments, "We are pleased by the progress of both our Phase 2 clinical trials for our universal influenza vaccine and are on track to announce top line data in early 2020. There remains a pressing need to find an effective universal vaccine across all A virus strains that can be manufactured at speed and we believe that our VTP-100 product is a potential solution to this global health issue."
The FLU010 clinical study has been funded in part with Federal funds from the Department of Health and Human Services; Office of the Assistant Secretary for Preparedness and Response; Biomedical Advanced Research and Development Authority, under Contract No. HHSO100201900013C.
About Vaccitech’s Platform and Influenza Programme
Vaccitech’s VTP-100 vaccine candidate aims to prevent pandemic and seasonal influenza by eliciting broad and durable immune protection against all "A strains" of the virus, which cannot be achieved by traditional vaccination. The vaccine consists of MVA, a replication deficient pox viral vector that has been safely tested in thousands of patients, to generate a strong immune reaction against Matrix 1 (M1) and Nucleoprotein (NP) influenza antigens. The antigens are highly conserved between influenza A viral subtypes and their intramuscular delivery in Vaccitech’s MVA vector construct induces a potent cell-mediated immune response intended to reduce the likelihood of developing clinical illness from influenza.
About Vaccitech Ltd and Vaccitech Australia Limited Pty
Vaccitech Ltd develops immunotherapies to treat cancer and infectious disease. The company holds the rights to proprietary technology refined through over twenty years of research performed at Oxford University’s Jenner Institute, among the world’s most prestigious vaccine research centre. Vaccitech is developing a T cell induction platform that can elicit an unprecedented CD8+ T cell response against clinically relevant antigenic targets. The platform is applied in numerous infectious diseases and oncology programs and ...
(All Rights Reserved)