Multiple Ascending Dose Study of BMS-582949 in Patients With Stable Rheumatoid Arthritis on the Methotrexate Background
Completed · Phase 1
Conditions studied: Rheumatoid Arthritis
In brief
The purpose of this clinical research study is to learn if it is safe for rheumatoid arthritis patients to take BMS-582949 along with methotrexate.
Key facts
- Study ID
- NCT00162292
- Run by
- Bristol-Myers Squibb
- People needed
- 33
- Starts
- 2005-11-01
- Expected to finish
- 2007-10-01
- Last updated by the study team
- 2010-03-02
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18-70 years
- Diagnosis of RA for ≥6 months
- Swollen or tender joint or ESR >ULN. Subject must be on stable doses of MTX
- Women of Childbearing Potential
You may not qualify if…
- Serum transaminase levels >ULN
- CK>ULN
- Cannot have taken Orencia or Remicade within 8 weeks of baseline, Humira or Enbrel within 4 weeks of baseline
- Use of H2 blockers or Proton Pump inhibitors while on study
Where it is running
- Desert Medical Advances — Palm Desert, California, United States
- Boling Clinical Trials — Upland, California, United States
- Delray Research Associates — Delray Beach, Florida, United States
- Ocala Rheumatology Research Center — Ocala, Florida, United States
- Phase Iii Clinical Research — Fall River, Massachusetts, United States
- Covance Clinical Research Unit Inc. — Dallas, Texas, United States
- Radiant Research San Antonio Northeast — San Antonio, Texas, United States
- Healthcare Discoveries, Inc — San Antonio, Texas, United States
- Local Institution — León, Guanajuato, Mexico
- Local Institution — Metepec, State of Mexico, Mexico
Full record on ClinicalTrials.gov
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