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

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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.


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
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2361
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Bethlehem, PA
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Brooklyn, NY
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Carrollton, TX
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Charleston, South Carolina 29412
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Covina, CA
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Duncansville, Pennsylvania 16635
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Soifia,
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Whittier, CA
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