Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Pivagabine is a small molecule psychoactive drug classified as an antidepressant and anxiolytic. It was introduced in Italy in 1997 under the brand name Tonerg for the treatment of depressive and maladaptive syndromes but has since been discontinued. Pivagabine is a hydrophobic derivative of 4-aminobutyric acid (GABA). Although initially thought to act as a prodrug for GABA, its mechanism is now believed to involve modulation of corticotropin-releasing factor (CRF) and antagonism of stress-induced changes in GABAA receptor function. Preclinical studies demonstrated that pivagabine crosses the blood-brain barrier, does not undergo metabolic transformation, exhibits low toxicity, prevents stress-induced convulsions in animal models, and reduces anxiety-related behaviors. In clinical settings, it showed efficacy in reducing psychological distress associated with inadequate management of stressful events[1][4][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 pivagabine.