drugset / Trial / NCT03240809

An Open-label, Single-dose Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Brodalumab in Pediatric Subjects

NCT03240809

Phase 4 Active not recruiting 2 enrolled Bausch Health Americas, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

An Open-label, Single-dose Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Brodalumab in Pediatric Subjects

Timeline

Start
2020-01-24
Primary completion
2028-12
Completion
2029-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Brodalumab Monoclonal antibody 70 mg Subcutaneous
Subject Brodalumab Monoclonal antibody 140 mg Subcutaneous

Indications