Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Quinidine phenobarbital** is a historical oral fixed-dose combination of the class Ia antiarrhythmic quinidine and the barbiturate phenobarbital, also indexed as quinidine barbiturate and quinidine phenylethylbarbiturate. Quinidine produces use-dependent cardiac sodium-channel blockade and inhibits potassium currents, slowing conduction and prolonging refractoriness; phenobarbital enhances inhibitory gamma-aminobutyric acid signaling through gamma-aminobutyric acid type A receptors and can inhibit excitatory AMPA-type glutamate receptors. The combination was marketed in tablet form, including as Natisedine, for rhythm-related palpitations and extrasystoles associated with anxiety, irritability, and insomnia. It is a 1:1 quinidine-phenobarbital complex with molecular formula C32H36N4O5. ([pubchem.ncbi.nlm.nih.gov](https://pubchem.ncbi.nlm.nih.gov/compound/Quinidine-phenobarbital))
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 quinidine phenobarbital.