Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
VesiculoVax Ebola (also known as VesiculoVax Vectored EBOV Vaccine) is a mono-valent, replication-competent viral vector vaccine developed by Auro Vaccines in partnership with Emergent BioSolutions for the prevention of Ebola virus disease (EVD). The vaccine utilizes a highly attenuated recombinant vesicular stomatitis virus (rVSV) vector—the prototype of the VesiculoVax platform—engineered to express the Zaire ebolavirus glycoprotein (GP) as its active immunogen. Upon administration, the replication-competent vector activates the immune system through innate signals and the release of molecular adjuvants, triggering the rapid expansion of B cells and the production of protective antibodies. The platform is characterized by low pre-existing immunity in the human population compared to adenovirus-based vectors. Clinical evaluation has progressed through Phase 1, where the vaccine demonstrated safety, 100% vaccine take, and immunogenicity across a range of doses.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on VesiculoVax Ebola.