drugset / Trial / NCT01893528

Study to Assess the Safety and Tolerability of Ascending Single Doses of REGN2009 in Healthy Volunteers

NCT01893528 ↗

Phase 1 Completed 49 enrolled Regeneron Pharmaceuticals
RandomizedSingle-groupTriple-blindTreatment

Summary

This is a phase 1, randomized, double-blind, placebo-controlled first-in-human (FIH) study to assess the safety and tolerability of ascending single doses of REGN2009 administered to healthy volunteers.

Timeline

Start
2013-06
Primary completion
2014-09
Completion
2014-09

Drugs

EvaluationDrugModalityDoseRoute
Subject REGN2009 Unknown — —

Indications

No indication recorded.