UM171 Expanded Cord Blood In Patients With High-Risk Acute Leukemia/Myelodysplasia

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

April 1, 2019

Primary Completion Date

October 31, 2024

Study Completion Date

October 31, 2027

Conditions
High Risk Hematologic MalignancyCord Blood Transplant
Interventions
BIOLOGICAL

Transplant with an expanded ECT-001 cord blood

"1. Patients will receive a conditioning regimen (such as: cyclophosphamide 120 mg/kg, fludarabine 75mg/m2 and TBI 12 Gy or cyclophosphamide 50 mg/kg, fludarabine 150 mg/m2, thiotepa 10 mg/kg and TBI 4 Gy).~2. The cord to be expanded will undergo CD34+ selection. The CD34- product is cryopreserved and will be thawed and infused on Day +1 post-transplant. The CD34+ product will be placed in a closed culture with UM171 for a 7-day expansion and is infused on Day 0.~3. Patients will receive standard supportive care and GVHD prophylaxis (such as MMF and tacrolimus). Tacrolimus will be discontinued on Day 100 post-transplant unless GVHD arises."

Trial Locations (1)

H1T2M4

CIUSSS de l'Est-de-l'île-de Montreal, Hôpital Maisonneuve-Rosemont, Montreal

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Stem Cell Network

OTHER

collaborator

ExCellThera inc.

INDUSTRY

lead

Ciusss de L'Est de l'Île de Montréal

OTHER

NCT03913026 - UM171 Expanded Cord Blood In Patients With High-Risk Acute Leukemia/Myelodysplasia | Biotech Hunter | Biotech Hunter