Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AVAT-122 (formerly SAP-022) is an aqueous solution formulation of synthetic cannabidiol (CBD) being developed by Avata Biosciences (formerly Sapient Therapeutics) for the treatment of pediatric focal epilepsy. Utilizing Avata's proprietary water-soluble cannabinoid formulation technology, AVAT-122 is designed to improve the bioavailability and delivery of cannabidiol without the use of oil, alcohol, or THC. Cannabidiol acts as a multi-target modulator, primarily targeting cannabinoid receptors 1 and 2 (CB1 and CB2), G-protein coupled receptor 55 (GPR55), and transient receptor potential vanilloid type 1 (TRPV1) channels to reduce neuronal hyperexcitability. AVAT-122 is currently in Phase 1 clinical development.
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 AVAT-122.