Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Albis is a fixed-dose combination therapy developed by Daewoong Pharmaceutical, primarily used for the treatment and prevention of gastric and duodenal ulcers, as well as gastritis. It contains three active ingredients: ranitidine, bismuth potassium citrate, and sucralfate. Ranitidine acts as a histamine H2-receptor antagonist to reduce gastric acid secretion. Bismuth potassium citrate provides cytoprotective effects and possesses antimicrobial activity against *Helicobacter pylori*. Sucralfate forms a physical barrier over ulcerated tissue, protecting it from further damage by acid, pepsin, and bile salts. This combination is designed to provide synergistic effects in acid suppression and mucosal protection. In 2019, Albis was withdrawn from the South Korean market following a regulatory suspension of all ranitidine-containing products due to the detection of N-nitrosodimethylamine (NDMA) impurities.
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 Albis.