drugset / Trial / NCT00534313

Safety and Efficacy of Abatacept Versus Placebo in Participants With Psoriatic Arthritis

NCT00534313 ↗

Phase 2 Terminated 191 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine an optimal abatacept dosing regimen for the treatment of active arthritis due to psoriatic arthritis in patients who have had a prior inadequate response to disease-modifying antirheumatic drugs, including methotrexate and tumor necrosis factor alpha-blockade compounds.

Timeline

Start
2007-11
Primary completion
2008-12
Completion
2011-05

Outcome

Outcome not reported

Stopped: “Lack of efficacy with respect to skin-related lesions in the short-term phase”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Abatacept Other / unclassified 3 mg/kg Intravenous
Comparator Abatacept Other / unclassified 10 mg/kg Intravenous

Indications