Clinical trial

Study Evaluating ERB-041 With Methotrexate in Rheumatoid Arthritis

NCT00141830 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Completed

Key facts

NCT number NCT00141830
Title Study Evaluating ERB-041 With Methotrexate in Rheumatoid Arthritis
Official title A Randomized, Parallel, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of 3 Oral Doses of ERB-041 in Subjects With Rheumatoid Arthritis on a Background of Methotrexate Therapy
Lead sponsor Wyeth is now a wholly owned subsidiary of Pfizer, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Rheumatoid Arthritis
Intervention type Drug
Interventions Methotrexate plus ERB-041 for 12 weeks, Placebo for 12 weeks
Enrollment 159
Start date Aug 1, 2005
Primary completion Oct 19, 2006
Completion Oct 19, 2006
First posted Sep 1, 2005
Last update posted Sep 29, 2020
Countries Canada, Hungary, Italy, Mexico, Spain, United States

At a glance

  • 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:

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