drugset / Trial / NCT02741739

Study of the Blood Concentrations of Two Formulations of REGN1033 in Healthy Subjects

NCT02741739

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

Summary

Primary Objective: Determine blood concentrations of two formulations of REGN1033. Secondary Objective: Assess safety and tolerability of REGN1033.

Timeline

Start
2016-03
Primary completion
2016-04
Completion
2016-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Trevogrumab Monoclonal antibody Subcutaneous

Indications

No indication recorded.