Overview

Phase I Study to Assess the Tolerability and Efficacy of Nivolumab in Patients With Hematologic Malignancies

Status:
Terminated
Trial end date:
2020-06-22
Target enrollment:
Participant gender:
Summary
This is an open-label, dose escalation Phase I study to evaluate the tolerability and efficacy of single agent of Nivolumab as maintenance treatment to prevent relapse in patients with hematologic malignancies after allogeneic stem cell transplantation. Approximately 29 patients will be enrolled, where about 6-12 patients will be included on the dose escalation phase and 20 patients will be on the expansion cohort at maximal tolerated dose.
Phase:
Phase 1
Details
Lead Sponsor:
University of Chicago
Treatments:
Antibodies, Monoclonal
Nivolumab