drugset / Trial / NCT01810718

Phase I/II for Safety and Efficacy of Nilotinib in a Population Steroid-refractory/or Steroid-dependent cGVHD

NCT01810718

Phase 1 Completed 22 enrolled Italian Group for Bone Marrow Transplantation
NaSingle-groupOpen-labelTreatment

Summary

Chronic Graft versus Host Disease (cGvHD) has been identified as the leading cause of late non-relapse mortality in Hemopoietic Stem Cell Transplant (HSCT) survivors. Up to now a standard satisfactory treatment for these patients does not exist. cGVHD is an immune-mediated disease, resulting from a complex interaction between donor and recipient adaptive immunity, but its exact pathogenesis is still incompletely defined. The purpose of this study is to determine safety and efficacy of Nilotinib in a population with steroid-refractory/or steroid-dependent cGvHD with a phase I study. In phase II the MTD will be used to define the efficacy of Nilotinib in a cGvHD steroid- refractory or steroid dependent population, with the same characteristics of the previously Imatinib-treated population.

Timeline

Start
2011-11
Primary completion
2015-02
Completion
2016-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Nilotinib Small molecule 200 mg
Subject Nilotinib Small molecule 300 mg