Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**NMRC-MV-Ad-PfC + NMRC-M3V-Ad-PfCA** is an investigational combination malaria vaccine composed of two replication-deficient recombinant adenovirus serotype 5 vectors. One vector (NMRC-MV-Ad-PfC) encodes the *Plasmodium falciparum* circumsporozoite protein (CSP), and the other (NMRC-M3V-Ad-PfCA) encodes both CSP and apical membrane antigen-1 (AMA1) from the 3D7 strain of *P. falciparum*. Both vaccine components are designed to elicit robust cell-mediated (primarily CD8+ T cell) and humoral immune responses against key malaria antigens, targeting both pre-erythrocytic (CSP) and erythrocytic (AMA1) parasite stages. The vaccine regimen involves co-formulating equal amounts of each vector and administering them together via intramuscular injection. The vaccine has been evaluated in Phase 1 and 2a clinical trials for safety, tolerability, immunogenicity, and efficacy in healthy, malaria-naïve adults, and is noted for its strong T cell immunogenicity, though it has not achieved sterile protective immunity in challenge studies[1][4][5][7][8][10].
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 NMRC-MV-Ad-PfC + NMRC-M3V-Ad-PfCA.