drugset / Trial / NCT01930162

Safety and Tolerability of HSC835 in Patients With Hematological Malignancies Undergoing Single Umbilical Cord Blood Transplant

NCT01930162

Phase 2 Completed 9 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelBasic science

Summary

This study was designed to evaluate the safety and tolerability of HSC835 for clinical use as measured by the absence of graft failure at day 42 in excess of that currently observed with double umbilical cord blood (UCB) transplantation (DUCBT) with non-myeloablative (NMA) conditioning.

Timeline

Start
2014-10-07
Primary completion
2016-08-29
Completion
2016-08-29

Drugs

EvaluationDrugModalityDoseRoute
Subject HSC835 Cell therapy