Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**APEX-002** (also designated APEX-52) is a low-dose, orally administered synthetic **psilocybin** formulation developed by **Apex Labs** for take-home use in treating mental health disorders. It acts primarily as a **serotonin 5-HT2A receptor agonist** and **ATP-binding cassette transporter modulator**, potentially offering therapeutic benefits for depression and anxiety with reduced psychoactive effects due to microdosing. Apex Labs has advanced multiple clinical studies, including IND submission to the FDA for pharmacokinetic and driving performance assessments, and Health Canada approvals for phase 2b trials evaluating efficacy in PTSD-associated depression.[1][3][5][9][11]
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 APEX-002.