drugset / Trial / NCT00873860

Study to Evaluate the Safety and Efficacy of CAT-354

NCT00873860

Phase 2 Completed 357 enrolled MedImmune LLC
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase 2a, randomized, double-blind, placebo-controlled, parallel-arm study to evaluate the efficacy and safety of 3 subcutaneous (SC) treatment regimens of CAT-354 in adult subjects with uncontrolled, moderate-to-severe, persistent asthma.

Timeline

Start
2009-06
Primary completion
2010-08
Completion
2010-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Tralokinumab Monoclonal antibody 150 mg Subcutaneous
Subject Tralokinumab Monoclonal antibody 300 mg Subcutaneous
Subject Tralokinumab Monoclonal antibody 600 mg Subcutaneous

Indications