Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
5-MeO-DMT (5-methoxy-N,N-dimethyltryptamine) is a potent, fast-acting psychedelic tryptamine that acts as a non-selective serotonin receptor agonist, with particularly high affinity for the 5-HT1A and 5-HT2A subtypes. Benuvia operates as a contract development and manufacturing organization (CDMO) that produces high-purity, synthetic, GMP-grade 5-MeO-DMT for use by pharmaceutical and biotech clients in clinical research. The compound is currently being investigated for its therapeutic potential in treating psychiatric conditions such as treatment-resistant depression, anxiety, and post-traumatic stress disorder (PTSD). Unlike longer-acting psychedelics like psilocybin, 5-MeO-DMT is characterized by a rapid onset and short duration of action, often lasting less than 30 minutes.
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 5-MeO-DMT.