Clinical trial
Efficacy and Safety of Lumiracoxib in Patients With Primary Knee Osteoarthritis…
NCT00367315 · Novartis, Industry · Completed
Key facts
| NCT number | NCT00367315 |
|---|---|
| Title | Efficacy and Safety of Lumiracoxib in Patients With Primary Knee Osteoarthritis (OA) |
| Official title | A 13-week, Multicenter, Randomized, Double-blind, Double-dummy, Placebo-controlled, Parallel Trial of 2 Different Dose Regimens of Lumiracoxib (100 mg od and 200 mg od Initial Dose for Two Weeks Followed by 100 mg od) in Patients With Primary Knee Osteoarthritis, Using Celecoxib (200 mg od) as a… |
| Lead sponsor | Novartis, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Knee Osteoarthritis |
| Intervention type | Drug |
| Interventions | Lumiracoxib |
| Enrollment | 1,684 |
| Start date | Sep 1, 2003 |
| Primary completion | Feb 1, 2004 |
| First posted | Aug 22, 2006 |
| Last update posted | May 21, 2012 |
| Countries | Germany, Switzerland |
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: