Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**XP21279** is an orally administered, sustained-release **levodopa prodrug** developed by XenoPort for Parkinson's disease with motor fluctuations. It was designed to improve the gastrointestinal absorption profile of levodopa: XP21279 is actively transported by high-capacity nutrient transporters along the gastrointestinal tract and is rapidly hydrolyzed by carboxylesterases to release levodopa. The resulting levodopa is converted to dopamine in the central nervous system, restoring dopaminergic neurotransmission. Clinical development evaluated sustained-release bilayer XP21279 tablets administered with carbidopa; Phase 2 testing showed reduced levodopa concentration variability versus immediate-release carbidopa-levodopa, but no statistically significant improvement in off time.
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 XP21279.