Overview

Study Evaluating ERB-041 With Methotrexate in Rheumatoid Arthritis

Status:
Completed
Trial end date:
2006-10-19
Target enrollment:
Participant gender:
Summary
The primary objective of this study is to compare the efficacy and safety of 3 dose levels of oral ERB-041 administered daily for 12 weeks versus placebo in subjects with active rheumatoid arthritis who have had a suboptimal response to therapy with stable doses of methotrexate (MTX).
Phase:
Phase 2
Details
Lead Sponsor:
Wyeth is now a wholly owned subsidiary of Pfizer
Treatments:
Methotrexate