drugset / Trial / NCT00788294

Measure Exposure Of Tanezumab In Healthy Volunteers When Administering The Drug Subcutaneously

NCT00788294

Phase 1 Completed 76 enrolled Pfizer
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The hypothesis of this study is that subcutaneous administration of tanezumab results in lower drug exposure compared to intravenous administration of tanezumab.

Timeline

Start
2008-11
Primary completion
2009-06
Completion
2009-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Tanezumab Monoclonal antibody 5 mg Intravenous
Comparator Tanezumab Monoclonal antibody 10 mg Intravenous
Comparator Tanezumab Monoclonal antibody 19 mg Intravenous

Indications

No indication recorded.