drugset / Trial / NCT01061736

Evaluation of Sarilumab (SAR153191/REGN88) on Top of Methotrexate in Rheumatoid Arthritis Patients

NCT01061736 ↗

Phase 2/3 Completed 1675 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

Primary Objectives: Part A (dose ranging study): To demonstrate that sarilumab (SAR153191/REGN88) on top of MTX was effective on reduction of signs and symptoms of rheumatoid arthritis at 12 weeks. Part B (pivotal study): To demonstrate that sarilumab added to MTX was effective in: * reduction of signs and symptoms of rheumatoid arthritis at 24 weeks * inhibition of progression of structural damage at 52 weeks * improvement in physical function at 16 weeks Secondary Objectives: Part B: To demonstrate that sarilumab added to MTX was effective in induction of a major clinical response at 52 weeks To assess the safety of sarilumab added to MTX To document the pharmacokinetic profile of sarilumab added to MTX in participants with active rheumatoid arthritis who were inadequate responders to MTX therapy.

Timeline

Start
2010-03
Primary completion
2013-10
Completion
2013-10

Outcome

Met primary endpoint

registry Part A: SAR 150 mg qw vs Part A: Placebo qw; p = 0.0041; Odds Ratio (OR) 3.84 (95% CI 1.53 to 9.63) NCT01061736 ↗

registry Part B: SAR 150 mg q2w vs Part B: Placebo q2w; p <0.0001; Odds Ratio (OR) 2.773 (95% CI 2.077 to 3.703) NCT01061736 ↗

registry Part B: SAR 150 mg q2w vs Part B: Placebo q2w; p <0.0001; LS mean difference -0.235 (95% CI -0.312 to -0.157) NCT01061736 ↗

registry Part B: SAR 150 mg q2w vs Part B: Placebo q2w; p <0.0001; Rank ANCOVA NCT01061736 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Sarilumab Monoclonal antibody 100 mg Subcutaneous
Subject Sarilumab Monoclonal antibody 150 mg Subcutaneous
Subject Sarilumab Monoclonal antibody 200 mg Subcutaneous
Background Methotrexate Small molecule — —
Background folic acid Other / unclassified — —

Indications