drugset / Trial / NCT01540539

Intravenous/Subcutaneous FIH Study of REGN1154 in Healthy Volunteers

NCT01540539 ↗

Phase 1 Completed 44 enrolled Regeneron Pharmaceuticals
RandomizedParallel-groupTriple-blind

Summary

The purpose of this study is to study the safety and tolerability of intravenous (IV) and subcutaneous (SC) administration of REGN1154 in normal healthy subjects.

Timeline

Start
2012-03
Primary completion
2013-01
Completion
2013-01

Drugs

EvaluationDrugModalityDoseRoute
Subject REGN1154 Unknown — Intravenous

Indications

No indication recorded.