Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This therapeutic intervention consists of a combination of synthetic psilocybin and transcutaneous auricular vagus nerve stimulation (taVNS) for the treatment of major depressive disorder (MDD). Psilocybin is a serotonergic psychedelic that acts as a prodrug for psilocin, which primarily targets the 5-HT2A receptor to facilitate rapid neuroplasticity and profound psychological shifts. The taVNS component is a non-invasive medical device that delivers electrical stimulation to the auricular branch of the vagus nerve, aiming to modulate autonomic tone and enhance the therapeutic window provided by psilocybin. Developed by Dr. Charles Raison and investigated in the OPTIMIZE Phase 2 clinical trial, this approach explores whether neuromodulation can sustain or amplify the antidepressant effects of a single 25 mg psychedelic dose.
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 psilocybin + transcutaneous auricular vagus nerve stimulation.