Study of hCT-MSC in Newborn Infants With Moderate or Severe HIE

PHASE1CompletedINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

December 27, 2018

Primary Completion Date

July 28, 2019

Study Completion Date

December 28, 2020

Conditions
Moderate to Severe Hypoxic-ischemic Encephalopathy
Interventions
BIOLOGICAL

Infusion of hCT-MSC

Infants who meet enrollment criteria for moderate to severe hypoxic ischemic encephalopathy will receive 1 infusion of hCT-MSC within the first 48 postnatal hours. hCT-MSCs are a product of allogeneic cells manufactured from digested umbilical cord tissue that is expanded in culture, cryopreserved and banked. hCT-MSCs are manufactured from umbilical cord tissue donated to the Carolinas Cord Blood Bank, an FDA-licensed, FACT-accredited, public cord blood bank at Duke University Medical Center, after written informed consent from the baby's mother. Cord tissue is harvested from the placentas of male babies delivered by elective C-section after a normal, full- term pregnancy.

Trial Locations (1)

27705

Duke University, Durham

All Listed Sponsors
collaborator

Duke Clinical and Translational Science Institute (CTSI), part of the NIH Clinical and Translational Science Awards (CTSA)

UNKNOWN

lead

Joanne Kurtzberg, MD

OTHER

NCT03635450 - Study of hCT-MSC in Newborn Infants With Moderate or Severe HIE | Biotech Hunter | Biotech Hunter