Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Valnoctamide is a small molecule derivative of valproic acid, classified as a fatty amide and structurally related to the anticonvulsant drug valpromide. Unlike valpromide, it is not metabolized into its corresponding acid in vivo. Valnoctamide has been used since the 1960s in Europe as a sedative-hypnotic and anxiolytic, marketed under brand names such as Nirvanil and Axiquel. It has also been investigated for use in epilepsy, neuropathic pain, mania (including bipolar disorder), and schizoaffective disorder. Preclinical studies suggest that all four stereoisomers of valnoctamide are more effective than valproic acid in animal models of epilepsy. Mechanistically, it is believed to act primarily through modulation of GABAergic neurotransmission—likely by inhibiting GABA transaminase—and may also inhibit histone deacetylases (HDACs). Notably, compared to other drugs in its class such as valproate/valproic acid, it exhibits significantly lower teratogenicity[1][3][4][6].
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 valnoctamide.