drugset / Trial / NCT02350751

Phase 1 Placebo-controlled,Dose-escalation Study to Evaluate the Safety and Pharmacokinetics of MEDI8852 in Adults

NCT02350751

Phase 1 Completed 94 enrolled MedImmune LLC
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the safety and pharmacokinetics of MEDI8852 compared to placebo when administered to healthy adult subjects.

Timeline

Start
2015-01
Primary completion
2015-06
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject MEDI8852 Monoclonal antibody 250 mg Intravenous
Subject MEDI8852 Monoclonal antibody 750 mg Intravenous
Subject MEDI8852 Monoclonal antibody 1500 mg Intravenous
Subject MEDI8852 Monoclonal antibody 3000 mg Intravenous

Indications