Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Proxibarbal is a barbiturate derivative that functions as a sedative and enzyme inducer, notably lacking the potent hypnotic effects typical of the barbiturate class. It exists in a rapid tautomeric equilibrium with valofan (2-allophanyl-2-allyl-gamma-valerolactone), which acts as its cerebral prodrug. Historically, it has been utilized in the treatment of migraine, menopausal psycho-neuro-autonomic disorders, and various psychosomatic conditions. While it was investigated for the prophylaxis of gastro-duodenal ulcer recurrence, clinical trials did not demonstrate statistical significance. A significant clinical concern associated with its use is the development of immuno-allergic thrombocytopenia.
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 proxibarbal.