drugset / Trial / NCT07283822

Amping up With PemJAK

NCT07283822

Phase 2 Recruiting 53 enrolled Seda S. Tolu Incyte Corporation · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to understand and determine if ruxolitinib added to pembrolizumab is safe and effective for the treatment of relapsed or refractory Hodgkin and non-Hodgkin lymphomas.

Timeline

Start
2025-12-03
Primary completion
2028-01
Completion
2029-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Pembrolizumab Monoclonal antibody 200 mg Intravenous
Subject Ruxolitinib Small molecule 20 mg Oral