drugset / Trial / NCT02874092

Ticagrelor in Methotrexate-Resistant Rheumatoid Arthritis

NCT02874092

Phase 4 Completed 9 enrolled NYU Langone Health
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is an open label study to assess the improvement in the Disease Activity Score for 28-joint counts (DAS28) with ticagrelor given at 90 mg twice daily in patients with RA who have active disease despite MTX therapy (as defined by the inclusion/exclusion criteria). There will also be a cross sectional analysis of baseline platelet activity in subjects with rheumatoid arthritis and osteoarthritis. Subjects in the OA cohort will not receive any study medication, and will only have one study visit. Patients will receive 90 mg ticagrelor orally bid. The patients will receive drug for 30-days. Methotrexate dose will remain stable throughout the study duration.

Timeline

Start
2016-11-15
Primary completion
2019-04-19
Completion
2019-06-19

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ticagrelor Small molecule 90 mg Oral
Comparator MTX therapy Unknown 10 mg
Comparator MTX therapy Unknown 25 mg

Indications