drugset / Trial / NCT02999711

Study of Safety, Tolerability, and Pharmacokinetics of Multiple Ascending Doses of REGN3500 in Adults With Moderate Asthma

NCT02999711

Phase 1 Completed 23 enrolled Regeneron Pharmaceuticals Sanofi · collab
RandomizedParallel-groupQuadruple-blindOther

Summary

Purpose of this study is to assess the safety and tolerability of multiple ascending subcutaneous doses of REGN3500 to moderate asthmatics.

Timeline

Start
2017-02-03
Primary completion
2018-08-30
Completion
2018-09-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Itepekimab Monoclonal antibody 75 mg Subcutaneous
Subject Itepekimab Monoclonal antibody 150 mg Subcutaneous

Indications