Clinical trial
12-Week, Double-Blind, Placebo-Controlled, Randomized Study of the Efficacy of…
NCT00456586 · Kyowa Kirin, Inc., Industry · Completed
Key facts
| NCT number | NCT00456586 |
|---|---|
| Title | 12-Week, Double-Blind, Placebo-Controlled, Randomized Study of the Efficacy of 40 mg/Day KW-6002 in Parkinson's Disease Patients on Levodopa/Carbidopa |
| Official title | A 12-Week, Double-Blind, Placebo-Controlled, Randomized, Multicenter Study of the Efficacy of 40 mg/Day KW-6002 as Treatment for Parkinson's Disease in Patients With Motor Response Complications on Levodopa/Carbidopa Therapy |
| Lead sponsor | Kyowa Kirin, Inc., Industry |
| Status | Completed |
| Phase | Phase 2 |
| Study type | Interventional |
| Conditions | Parkinson's Disease |
| Intervention type | Drug |
| Interventions | KW-6002 (istradefylline) |
| Enrollment | 180 |
| Start date | Apr 1, 2002 |
| Primary completion | May 1, 2003 |
| Completion | Jun 1, 2003 |
| First posted | Apr 5, 2007 |
| Last update posted | Apr 25, 2024 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: