Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**BCT-521** is an orally administered fixed-dose small-molecule cannabinoid combination containing cannabidiol and dronabinol, the pharmaceutical form of delta-9-tetrahydrocannabinol. Developed by Beckley Canopy Therapeutics for cancer-associated pain in patients receiving opioid standard of care, it was evaluated against placebo in a randomized, double-blind Phase 1/2 study in Poland. The product is intended to modulate endocannabinoid signaling, principally through cannabinoid receptors 1 and 2; delta-9-tetrahydrocannabinol is the direct cannabinoid receptor agonist component, while cannabidiol has broader modulatory pharmacology. The registered EU trial is listed as completed, with no marketed brand name or regulatory approval identified. ([clinicaltrialsregister.eu](https://www.clinicaltrialsregister.eu/ctr-search/trial/2019-001382-32/PL))
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 BCT-521.