Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PZ-018 (Qingxin Lotus Seed Granules) is a Traditional Chinese Medicine (TCM) candidate developed by Yunnan Baiyao Group. It is classified as a Category 3.1 new TCM, a regulatory pathway in China for modern formulations derived from ancient classic prescriptions. The drug is based on the "Qingxin Lianzi Yin" formula, which traditionally contains ingredients such as lotus seed, scutellaria, ginseng, and astragalus. It is intended for the treatment of symptoms associated with "heart-fire" and "damp-heat" patterns, including urinary frequency, turbid urine, and restlessness. As of 2024, the program has completed production validation and is in the process of drafting the NDA dossier for submission to the NMPA.
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 Qingxin Lotus Seed Granules.