drugset / Trial / NCT00844805

Infliximab for Treatment of Axial Spondyloarthritis (P05336 AM1)

NCT00844805 ↗

Phase 3 Completed 158 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study was to assess the proportion of participants in the infliximab plus naproxen arm versus the placebo plus naproxen arm, in a population of participants with moderate-to-severe active axial spondyloarthritis and disease duration of ≤3 years, who achieve the Assessment in Ankylosing Spondylitis (ASAS) partial remission criteria.

Timeline

Start
2009-09
Primary completion
2011-04
Completion
2011-09

Outcome

Met primary endpoint

paper A greater percentage of patients achieved ASAS partial remission in the IFX+NPX group (61.9%; 65/105) than in the PBO+NPX group (35.3%; 18/51) at week 28 (p=0.002) PMID 23696633 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Infliximab Monoclonal antibody 5 mg/kg Intravenous
Subject Naproxen Small molecule 1000 mg Oral