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A Study to Evaluate the Switch From Etanercept to Infliximab in Subjects With Moderate-to-Severe Psoriasis (Study P05133) (TANGO)

NCT00686595 PHASE4 COMPLETED Results posted

This study will evaluate the efficacy, tolerability, and effect on the quality of life of infliximab in adults with moderate-to-severe psoriasis who are resistant to etanercept after 12 weeks of treatment or have failed 24 weeks of treatment with etanercept. Infliximab will be administered as an intravenous infusion of 5 mg/kg at Baseline (Week 0), Visit 3 (Week 2), Visit 4 (Week 6), Visit 6 (Week 14), and Visit 8 (Week 22).

Details

Lead sponsorMerck Sharp & Dohme LLC
PhasePHASE4
StatusCOMPLETED
Enrolment48
Start dateMon Oct 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionThu Oct 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions