Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
QazCoVac-P is a recombinant protein subunit vaccine developed by the Research Institute for Biological Safety Problems (RIBSP) in Kazakhstan for the prevention of COVID-19. It is distinct from the institute's first vaccine, QazVac, which is an inactivated virus vaccine. QazCoVac-P utilizes a purified recombinant protein, typically the SARS-CoV-2 spike protein or a specific fragment such as the receptor-binding domain (RBD), to act as an antigen that stimulates the host's immune system. By introducing only a specific viral protein rather than the whole virus, the vaccine is designed to elicit protective neutralizing antibodies and cellular immune responses with a favorable safety profile. The vaccine has been evaluated in Phase I and Phase II clinical trials in Kazakhstan to assess its safety, tolerability, and immunogenicity in healthy adult volunteers, including the elderly population.
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 QazCoVac-P.