drugset / Trial / NCT02085473

A Study of Tralokinumab When Delivered Subcutaneously at Different Flow Rates to Healthy Volunteers

NCT02085473

Phase 1 Completed 60 enrolled MedImmune LLC
RandomizedParallel-groupOpen-labelOther

Summary

The primary objective of this study is to evaluate the pharmacokinetics (PK) and tolerability of tralokinumab when delivered subcutaneously at different flow rates to healthy volunteers.

Timeline

Start
2014-03-19
Primary completion
2014-07-10
Completion
2014-07-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Tralokinumab Monoclonal antibody 300 mg Subcutaneous

Indications