drugset / Trial / NCT01089725

Efficacy And Safety Study Of Tanezumab Subcutaneous Administration In Osteoarthritis - A Subcutaneous/Intravenous Bridging Study

NCT01089725

Phase 3 Terminated 385 enrolled Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

This is an efficacy and safety study of 3 doses (2.5 mg, 5 mg and 10mg) of tanezumab administered subcutaneously versus placebo. This study will also compare a subcutaneous (SC) administration of 10 mg of tanezumab) with an intravenous (IV) administration of 10 mg of tanezumab. Each person will receive an IV infusion and a SC infusion. The study will last 16 weeks for those who wish to enter a 64-week extension study or 24 weeks for those who do not.

Timeline

Start
2010-03-30
Primary completion
2010-11-08
Completion
2011-02-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Tanezumab Monoclonal antibody 2.5 mg Subcutaneous
Subject Tanezumab Monoclonal antibody 5 mg Subcutaneous
Subject Tanezumab Monoclonal antibody 10 mg Subcutaneous

Indications