drugset / Trial / NCT02305849

A Study to Evaluate Efficacy and Safety of ASP015K in Patients With Rheumatoid Arthritis (RA) Who Had an Inadequate Response to Methotrexate (MTX) Treatment

NCT02305849 ↗

Phase 3 Completed 519 enrolled Astellas Pharma Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of this study was to verify the efficacy of ASP015K versus placebo administrated in combination with methotrexate (MTX) over placebo in terms of efficacy in participants with rheumatoid arthritis (RA) who had an inadequate response to MTX

Timeline

Start
2014-07-25
Primary completion
2017-06-20
Completion
2017-11-28

Outcome

Met primary endpoint

paper Significantly more (p<0.001) peficitinib (58.6%, 100 mg; 64.4%, 150 mg) than placebo (21.8%) recipients achieved ACR20 response at week 12/ET. PMID 31350269 ↗

paper Significantly lower (p<0.001) mean changes from baseline in mTSS at week 28/ET occurred in peficitinib (1.62, 100 mg; 1.03, 150 mg) than placebo (3.37) recipients. PMID 31350269 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject peficitinib Small molecule 100 mg Oral
Subject peficitinib Small molecule 150 mg Oral
Background Methotrexate Small molecule — —

Indications