drugset / Trial / NCT03401671

Study of Lanadelumab in Healthy Japanese and Matched Caucasian Adult Subjects

NCT03401671

Phase 1 Completed 32 enrolled Shire
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the pharmacokinetics (PK), safety and tolerability and pharmacodynamics (PD) of lanadelumab in healthy adult Japanese subjects and matched non-Hispanic healthy adult Caucasian subjects.

Timeline

Start
2018-01-15
Primary completion
2018-05-30
Completion
2018-05-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Lanadelumab Monoclonal antibody 300 mg Subcutaneous

Indications

No indication recorded.