drugset / Trial / NCT01448239

Injection Site Tolerability, Safety, Pharmacokinetics and Pharmacodynamics Study After a Single Dose Subcutaneous Treatment of Alirocumab SAR236553 (REGN727)

NCT01448239

Phase 1 Completed 24 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

Primary Objective: Injection Site Tolerability Secondary Objectives: * To assess the safety profile of alirocumab SAR236553 (REGN727) * To assess the pharmacokinetic-pharmacodynamic relationship of alirocumab SAR236553 (REGN727)

Timeline

Start
2011-02
Primary completion
2011-05
Completion
2011-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Alirocumab Monoclonal antibody Subcutaneous

Indications