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This study is designed to provide safety and efficacy data to support the development of CP-690,550 in patients with moderate to severe rheumatoid arthritis on background of methotrexate.

Phase 3
Completed
Conditions
Health Condition 1: null- Arthritis, Rheumatoid
Registration Number
CTRI/2011/091/000575
Lead Sponsor
Pfizer Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
750
Inclusion Criteria

1. Ages Eligible for Study: 18 Years and older

2.Genders Eligible for Study: Both

3.Accepts Healthy Volunteers: No

4.Adults with moderate to severe rheumatoid arthritis on a stable dose of methotrexate

There is no upper age limit for inclusion criteria for this trial

Exclusion Criteria

Pregnancy, severe or unstable medical conditions, including serious infections (e.g., tuberculosis, HIV), clinically significant laboratory abnormalities (transaminases, hemoglobin), or use of prohibited concomitant medications (all DMARDs except methotrexate).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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