Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**CHI-541** is an investigational oral standardized cannabis extract supplied as an oil softgel. Each softgel contains approximately 2.5 mg total tetrahydrocannabinol and less than 0.25 mg cannabidiol, corresponding to an approximately 26:1 tetrahydrocannabinol-to-cannabidiol ratio. It was evaluated by Spectrum Therapeutics in a randomized, double-blind, placebo-controlled Phase 1a multiple-dose study in healthy adults, with proposed therapeutic applications including pain, nausea, muscle spasticity, and epilepsy. Its pharmacology is expected to be driven predominantly by tetrahydrocannabinol-mediated partial agonism of cannabinoid receptors 1 and 2. ([anzctr.org.au](https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=378769))
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 CHI-541.