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Clinical Trial Summary

The purpose of this trial is to evaluate the safety and efficacy of LY3009104 in participants with Rheumatoid Arthritis (RA).


Clinical Trial Description

This study consists of the following:

- Screening period: 4 to 28-days

- Part A: a 12-week blinded, placebo controlled treatment period

- Part B: a 12-week blinded extension period

- Part C: an optional 52-week open-label extension period

- Part D: an additional optional 52-week open-label extension period

- Follow up period: 28 days ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01185353
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 2
Start date October 2010
Completion date March 2014

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