Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**WD-1603** is an oral controlled-release fixed-dose combination of **carbidopa + levodopa** being developed for Parkinson's disease by Shanghai WD Pharmaceutical and Shanghai Hando Pharmaceutical Technology. The tablet uses proprietary GiPump osmotic delivery technology to provide bi-modal, sustained levodopa release and reduce peak-to-trough fluctuations in levodopa exposure. Carbidopa inhibits peripheral aromatic L-amino-acid decarboxylase, limiting peripheral conversion of levodopa to dopamine and increasing levodopa delivery to the brain; levodopa is then converted to dopamine to restore dopaminergic signaling. Phase II testing in early Parkinson's disease reported dose-dependent improvements in MDS-UPDRS II+III scores and relatively stable levodopa concentrations, while Phase III development has been reported as planned.
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 WD-1603.