drugset / Trial / NCT00856310

A Single-Dose Study of the Safety and Tolerability of REGN475(SAR164877) in Healthy Subjects

NCT00856310

Phase 1 Completed 56 enrolled Regeneron Pharmaceuticals Sanofi · collab
RandomizedSingle-groupTriple-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled single-dose study of the safety and tolerability of intravenously administered REGN475 in healthy volunteers. The primary objective of the study is to assess the safety and tolerability of REGN475. The secondary objectives are to characterize the pharmacokinetic and immunogenicity profiles of REGN475.

Timeline

Start
2009-02
Primary completion
2009-11
Completion
2009-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Fasinumab Monoclonal antibody Intravenous

Indications

No indication recorded.