Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**G03-52-01** is an investigational lyophilized, fixed-dose cocktail of six full-length human or humanized IgG1 monoclonal antibodies: three directed against botulinum neurotoxin serotype A and three directed against botulinum neurotoxin serotype B. The antibodies bind non-overlapping toxin epitopes, neutralizing the toxins and promoting their clearance; the product is being developed as a medical countermeasure for pre-exposure and potential post-exposure prophylaxis against botulism, including aerosolized exposure. It is composed of the three-antibody products NTM-1631 and NTM-1632 and has completed Phase 2 evaluation in healthy adults following intramuscular administration. ([pmc.ncbi.nlm.nih.gov](https://pmc.ncbi.nlm.nih.gov/articles/PMC13211578/))
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 G03-52-01.