Bavarian Nordic A/S (CPH:BAVA) (OTC:BVNRY), a fully integrated biotechnology company, announced on Tuesday the initiation of the first-in-human trial of MVA-BN WEV, a prophylactic vaccine candidate against the rare, but potentially deadly illness, the equine encephalitis virus.
This programme, which is funded by the US Department of Defence (DOD) Joint Project Manager for Chemical, Biological, Radiation, and Nuclear Medical (JPM CBRN Medical) is a multi-year agreement valued up to USD36m and aims to develop a vaccine against three separate strains of the equine encephalitis virus, Eastern (EEEV), Venezuelan (VEEV) and Western (WEEV), for which there are currently no preventative vaccines available.
According to the company, this phase 1 trial will evaluate the safety, tolerability and immunogenicity of MVA-BN WEV in 45 healthy adults in three treatment groups receiving different doses of the vaccine. Topline results from the study are expected to become available in 2020.
A successful phase 1, based on demonstrating a favourable safety and immunogenicity, could lead to follow-on funding, beyond the initial contract award of USD36m, to support further preclinical, clinical development and manufacturing to support licensure in the US.
Bavarian Nordic is focused on the development of innovative therapies against infectious diseases and cancer.
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Frontage expands early phase clinical research capabilities across US and China
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
InSysBio agrees new collaborative project with BeOne Medicines
Physiomics secures new modelling contract with Numab Therapeutics
Mabwell reports first patient dosed with 7MW4911 in US trial
Atossa Therapeutics' founder and CEO named one of The Top 50 Healthcare Technology CEOs of 2025
Avacta secures FDA clearance for second pre|CISION oncology programme
Guardant Health and Merck enter multi-year oncology diagnostics collaboration
Akeso secures NMPA review acceptance for gumokimab in ankylosing spondylitis