drugset / Trial / NCT00421915

Study Evaluating Etanercept Treatment of Patients With Ankylosing Spondylitis

NCT00421915

Phase 3 Completed 84 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of the study was to compare the efficacy of etanercept (25 mg, twice weekly) with that of placebo based on the percentage of patients who achieve the Assessment in Ankylosing Spondylitis (ASAS) response criteria (ASAS 20%) at week 12.

Timeline

Start
2002-03
Primary completion
Completion
2002-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Etanercept Protein / enzyme biologic 25 mg