Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PSY-007 is a small molecule NMDA receptor antagonist being developed by Psycheceutical Bioscience for the treatment of Post-Traumatic Stress Disorder (PTSD) and Complex Regional Pain Syndrome (CRPS). The drug is a patented topical formulation of ketamine that utilizes the company's proprietary NeuroDirect delivery technology. This platform is designed to deliver the medication topically to the sub-occipital region (the back of the neck), aiming to transport the active ingredient directly to the nervous system while bypassing the blood-brain barrier and systemic circulation. By targeting the nervous system directly, PSY-007 is intended to provide rapid therapeutic relief while minimizing the systemic exposure and dissociative side effects typically associated with traditional ketamine administration. PSY-007 is currently in Phase 1 clinical development for PTSD and in preclinical stages for CRPS.
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 PSY-007.