drugset / Trial / NCT02121080

Study of the Safety and Tolerability of REGN2222(SAR438584) in Healthy Adult Volunteers

NCT02121080 ↗

Phase 1 Completed 132 enrolled Regeneron Pharmaceuticals
RandomizedParallel-groupQuadruple-blindBasic science

Summary

This is a phase 1, randomized, double-blind, placebo-controlled study evaluating the safety, tolerability, pharmacokinetic (PK) profile, and immunogenicity of REGN2222 ascending in cohorts of healthy adult volunteers.

Timeline

Start
2014-05
Primary completion
2015-02
Completion
2015-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Suptavumab Monoclonal antibody — —

Indications

No indication recorded.