drugset / Trial / NCT01127893

Safety Extension Study Of Tanezumab When Administered By Subcutaneous Injection To Patients With Osteoarthritis

NCT01127893

Phase 3 Terminated 1 enrolled Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

An evaluation of the long term safety of tanezumab when administered by subcutaneous injection every 8 weeks for up to 64 weeks

Timeline

Start
2010-06-15
Primary completion
2010-09-29
Completion
2010-09-29

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