drugset / Trial / NCT02093923

A Double-Blind, Multiple Ascending Dose Study to Assess Safety, Tolerability and Pharmacokinetics of DX-2930 in Hereditary Angioedema Participants

NCT02093923

Phase 1 Completed 38 enrolled Shire
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) profile of multiple subcutaneous administrations of DX-2930 across a range of doses in HAE participants.

Timeline

Start
2014-05-14
Primary completion
2015-05-18
Completion
2015-05-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Lanadelumab Monoclonal antibody 30 mg Subcutaneous
Subject Lanadelumab Monoclonal antibody 100 mg Subcutaneous
Subject Lanadelumab Monoclonal antibody 300 mg Subcutaneous
Subject Lanadelumab Monoclonal antibody 400 mg Subcutaneous

Indications