drugset / Trial / NCT01860976

Efficacy and Safety of Subcutaneous Abatacept in Adults With Active Psoriatic Arthritis

NCT01860976

Phase 3 Completed 489 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to compare subcutaneous Abatacept to placebo in the treatment of psoriatic arthritis

Timeline

Start
2013-06-17
Primary completion
2015-07-14
Completion
2020-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Abatacept Other / unclassified 125 mg Subcutaneous

Indications