drugset / Trial / NCT02599207

Assessment of the Safety of Allogeneic Umbilical Cord Blood Infusions in Children With Cerebral Palsy

NCT02599207 ↗

Phase 1 Completed 15 enrolled Joanne Kurtzberg, MD
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study is a single site, phase I, prospective study of the safety of intravenous sibling cord blood infusion in 15 children ages 1-6 years with Cerebral Palsy (CP). All subjects will be treated with sibling cord blood cells. The first six will receive cord blood cells from an HLA-matched sibling. The following nine subjects will receive cord blood cells from an HLA-mismatched (≥3/6 match) or matched sibling. The duration of study participation will be six months from the time of the cord blood infusion.

Timeline

Start
2015-11
Primary completion
2016-10
Completion
2018-07

Drugs

EvaluationDrugModalityDoseRoute
Subject sibling umbilical cord blood Unknown — Intravenous

Indications