Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Sangzhi total alkaloids (SZ-A) is a botanical drug derived from the twigs of *Morus alba* L. (mulberry). Developed by the Institute of Materia Medica, Chinese Academy of Medical Sciences, and Beijing Wehand-Viamin Biotech, it was approved by the NMPA in China in 2020 as the first botanical drug for the treatment of type 2 diabetes mellitus (T2DM). The drug primarily acts as an alpha-glucosidase inhibitor, effectively lowering postprandial blood glucose by inhibiting the breakdown of complex carbohydrates in the small intestine. Its active components include polyhydroxyalkaloids such as 1-deoxynojirimycin (DNJ), fagomine, and 1,4-dideoxy-1,4-imino-D-arabinitol (DAB). Beyond glycemic control, it is currently being evaluated in Phase 4 clinical trials for its efficacy and safety in patients with diabetic nephropathy, focusing on renal function and albuminuria reduction.
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 sangzhi total alkaloids.