A MULTICENTER, RANDOMIZED, DOUBLE-BLIND COMPARISON OF 4 DOSE REGIMENS OF PLA-695, NAPROXEN, AND PLACEBO ADMINISTERED DAILY FOR 6 WEEKS IN SUBJECTS WITH ACTIVE OSTEOARTHRITIS OF THE KNEE

Update Il y a 4 ans
Reference: EUCTR2006-002590-44

Woman and Man

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Extract

To establish efficacy and safety of PLA-695 in subjects with active OA of the knee.


Inclusion criteria

  • ACTIVE OSTEOARTHRITIS OF THE KNEE