drugset / Trial / NCT00779935

Growth Factor Concentration to Predict an Ankylosing Spondylitis Patient's Response to Infliximab (Study P04041)(COMPLETED)

NCT00779935

Phase 4 Completed 44 enrolled Merck Sharp & Dohme LLC
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase 4, multi-center, open-label, one-arm, pilot study in patients with active ankylosing spondylitis refractory to conventional treatment. Remicade will be given at Weeks 0, 2, and 6 and then every 8 weeks up to Week 54. The number of patients showing ASAS-20 clinical response at Week 14 will be evaluated.

Timeline

Start
2004-10-01
Primary completion
2005-10-01
Completion
2007-02-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Infliximab Monoclonal antibody