Project Details
Description
A Phase 2, double-blind, placebo-controlled, randomized, parallel-group, multicenter study of the efficacy and safety of 40 mg/day KW-6002 as monotherapy in subjects w/PD
| Status | Finished |
|---|---|
| Effective start/end date | 6/15/05 → 12/15/06 |
Funding
- SYNEOS HEALTH, INC
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