Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Cannabidiol sulphate (LRP-661, CBDS) is a semi-synthetic, orally available derivative of cannabidiol (CBD) developed by London Research & Pharmaceuticals. It is designed to offer improved oral bioavailability and predictable pharmacokinetics compared to standard CBD formulations. LRP-661 demonstrates superior safety and efficacy in preclinical epilepsy models—including PTZ kindled mice and maximal electroshock seizure tests—showing enhanced gastrointestinal tolerability and absence of liver or renal toxicity relative to existing oral CBD solutions such as Epidiolex. The drug’s formulation allows for tablet and water-based solutions rather than oil suspensions. Its primary indication is epilepsy, with orphan drug applications being prepared for Dravet syndrome and Lennox-Gastaut syndrome[1][2][5][7].
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 cannabidiol sulphate.