drugset / Trial / NCT01026519

A Safety and Tolerability Study of REGN88(SAR153191) in Subjects With Rheumatoid Arthritis

NCT01026519

Phase 1 Completed 32 enrolled Regeneron Pharmaceuticals Sanofi · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a single-dose, double-blind, placebo-controlled, parallel group safety, tolerability and pharmacodynamic study of subcutaneously (SC) administered REGN88 in rheumatoid arthritis patients who are receiving concomitant methotrexate. Four (4) parallel groups of 8 subjects each with active rheumatoid arthritis will be dosed SC.

Timeline

Start
2008-09
Primary completion
2009-03
Completion
2009-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Sarilumab Monoclonal antibody Subcutaneous

Indications