drugset / Trial / NCT02613598

Dose Escalation Study to Determine the Maximum Tolerated Dose of the Combination of Ruxolitinib and Bortezomib in Patients With Relapsed or Refractory Lymphoma

NCT02613598

Phase 1 Completed 15 enrolled University of Michigan Rogel Cancer Center
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this research study is to determine the maximum tolerated dose (MTD) of Ruxolitinib (Jakafi) in combination with standard dose Bortezomib (Velcade) in patients with relapsed or refractory Hodgkin (HL) and Non-Hodgkin Lymphoma (NHL).

Timeline

Start
2016-05-12
Primary completion
2021-06-07
Completion
2021-06-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule 5 mg
Subject Ruxolitinib Small molecule 10 mg
Subject Ruxolitinib Small molecule 15 mg
Subject Ruxolitinib Small molecule 20 mg
Subject Ruxolitinib Small molecule 25 mg
Background Bortezomib Small molecule