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A 12-Week, Double-Blind, Randomized, Parallel Group, Placebo-Controlled Study of Two Doses of VX-702 in Subjects with Moderate to Severe Rheumatoid Arthritis

Update Il y a 4 ans
Reference: EUCTR2005-000549-13

Woman and Man

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Extract

- To define the clinical response to placebo and two doses of VX-702 in subjects with RA using the number of 20% responses as defined by the American College of Rheumatology (ACR20) at Week 12 by applying the Jonckheere-Terpstra trend analysis - To evaluate the safety and tolerability of 2 dose levels of VX-702 compared to placebo, when administered for 12 weeks to subjects with RA

Inclusion criteria

  • Rheumatoid Arthritis

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