Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**CDD-2103** is an investigational standardized Chinese herbal medicine comprising nine herbal ingredients, also referred to as modified Zhenwu decoction. Developed by Hong Kong Baptist University and its Centre for Chinese Herbal Medicine Drug Development, it is being evaluated primarily for maintenance of remission in ulcerative colitis, particularly in patients with the traditional Chinese medicine pattern of spleen deficiency with dampness accumulation. Preclinical colitis studies indicate that the formulation promotes an intestinal tolerogenic immune environment, including tolerogenic dendritic-cell-mediated regulatory T-cell differentiation, reduced inflammatory macrophage abundance, and improved epithelial barrier integrity through soluble guanylate cyclase-mediated cyclic guanosine monophosphate and protein kinase G signaling. CDD-2103 received National Medical Products Administration authorization for a clinical trial in China in August 2024; it is also planned for evaluation in diarrhea-predominant irritable bowel syndrome.
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 CDD-2103.