drugset / Trial / NCT01507402

A Study to Assess the Safety and Tolerability of Single Ascending Doses of REGN1033(SAR391786)

NCT01507402

Phase 1 Completed 76 enrolled Regeneron Pharmaceuticals Sanofi · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled, single ascending dose study to assess the safety and tolerability of Intravenous (IV) and Subcutaneous (SC) REGN1033(SAR391786) in healthy volunteers.

Timeline

Start
2012-01
Primary completion
2012-11
Completion
2012-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Trevogrumab Monoclonal antibody Intravenous

Indications

No indication recorded.