Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CBD-NE is a novel oral solid dosage formulation of cannabidiol (CBD) developed by DSM Nutritional Products (now part of dsm-firmenich). Utilizing the CBtru® platform, this formulation is delivered as a powder-filled capsule designed to overcome the bioavailability challenges and patient convenience issues associated with traditional oil-based CBD products. CBD is a non-psychoactive cannabinoid derived from the *Cannabis sativa* plant that interacts with the endocannabinoid system and various other molecular targets. DSM has evaluated CBD-NE in Phase 1 randomized, open-label pharmacokinetic studies to compare its absorption profile under both fed and fasted conditions against the FDA-approved CBD oral solution, Epidyolex. The formulation is being investigated for potential applications in epilepsy, insomnia, pain disorders, and other central nervous system diseases.
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 CBD-NE.