drugset / Trial / NCT02828397

Study of the Blood Concentrations of Two Formulations of REGN2222 in Healthy Subjects

NCT02828397 ↗

Phase 1 Completed 28 enrolled Regeneron Pharmaceuticals
RandomizedParallel-groupOpen-labelBasic science

Summary

Primary Objective: Determine blood concentrations of two formulations of REGN2222 Secondary Objective: Assess safety and tolerability of REGN2222

Timeline

Start
2016-04
Primary completion
2016-09
Completion
2016-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Suptavumab Monoclonal antibody — Intramuscular

Indications

No indication recorded.