Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Gremubamab is a first-in-class, bivalent, bispecific human immunoglobulin G1 kappa monoclonal antibody designed to target *Pseudomonas aeruginosa* infections. It selectively binds to two key virulence factors of *P. aeruginosa*: the PcrV protein (a component of the type III secretion system involved in host cell cytotoxicity) and the Psl exopolysaccharide (involved in bacterial colonization and tissue adherence). By targeting both these antigens, gremubamab aims to enhance neutrophil-mediated killing of *P. aeruginosa* and prevent associated cytotoxicity. The drug was developed primarily for prevention and treatment of nosocomial pneumonia (including ventilator-associated pneumonia) and bronchiectasis with chronic or high-risk *Pseudomonas* infection. Clinical development included phase 1 and phase 2 trials; however, further development for nosocomial pneumonia was discontinued due to safety/efficacy reasons.
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 gremubamab.