drugset / Trial / NCT00994890

A Long Term Study of the Safety of Tanezumab When Administered By Subcutaneous Injections

NCT00994890

Phase 2 Terminated 679 enrolled Pfizer
RandomizedParallel-groupDouble-blindOther

Summary

This study will investigate the safety of three fixed dose levels of tanezumab (2.5 mg, 5 mg, and 10 mg) administered at an 8-week interval by subcutaneous injection multiple (7) times during the study treatment period.

Timeline

Start
2009-11-17
Primary completion
2010-12-07
Completion
2011-03-01

Drugs

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