Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Dantonic Pill (T89) is a modernized botanical drug developed by Tasly Pharmaceutical Company. It is a formulation of extracts from Radix Salviae Miltiorrhizae (Danshen) and Radix Notoginseng (Sanqi), with Borneol added as an absorption enhancer. Primarily indicated for chronic stable angina pectoris due to coronary heart disease, it also shows potential in preventing and managing atherosclerosis. Its mechanism involves the downregulation of circulating adhesion molecules (CAMs) such as ICAM-1, VCAM-1, and E-selectin in the vascular endothelium, thereby inhibiting leukocyte adhesion and atherogenesis while improving coronary blood flow and microcirculation. It was the first traditional Chinese medicine to complete a Phase III clinical trial under an FDA IND in the United States.
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 Dantonic Pill.