drugset / Trial / NCT03002649

Study of Tofacitinib in Refractory Dermatomyositis

NCT03002649 ↗

Phase 1 Completed 10 enrolled Johns Hopkins University Pfizer · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to obtain preliminary data regarding the safety and efficacy of Janus kinase (JAK) inhibitor, tofacitinib, in adults with active, treatment-refractory dermatomyositis.

Timeline

Start
2017-01
Primary completion
2020-09-30
Completion
2020-09-30

Outcome

Met primary endpoint

paper At 12 weeks, the primary outcome was met in all 10 subjects. PMID 33258553 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Tofacitinib Small molecule 11 mg Oral

Indications