Long-term Safety and Efficacy of ABP 501 in Subjects With Moderate to Severe Rheumatoid Arthritis
Status: | Active, not recruiting |
---|---|
Conditions: | Arthritis, Rheumatoid Arthritis |
Therapuetic Areas: | Rheumatology |
Healthy: | No |
Age Range: | 18 - 81 |
Updated: | 4/21/2016 |
Start Date: | April 2014 |
End Date: | April 2016 |
An Open-label, Single-arm Extension Study to Evaluate the Long-term Safety and Efficacy of ABP 501 in Subjects With Moderate to Severe Rheumatoid Arthritis
The purpose of this open-label study is to evaluate the long-term safety and efficacy of ABP
501.
501.
Inclusion Criteria:
- Subject was randomized into protocol 20120262 and has completed the week 26 visit
Exclusion Criteria:
- Subject experienced a serious adverse event (SAE) or an adverse event (AE) in the
20120262 study that could cause extension treatment to be detrimental
- Subject has completed study 20120262 but cannot be dosed within 4 weeks of the week
26 visit of study 20120262
- Current infection requiring the use of oral or intravenous antibiotics
Other Inclusion/Exclusion criteria may apply
We found this trial at
31
sites
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