Genetically Modified T-cell Immunotherapy in Treating Patients With Relapsed/Refractory Acute Myeloid Leukemia and Persistent/Recurrent Blastic Plasmacytoid Dendritic Cell Neoplasm

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

December 15, 2015

Primary Completion Date

August 6, 2026

Study Completion Date

August 6, 2026

Conditions
Adult Acute Myeloid Leukemia in RemissionAcute Biphenotypic LeukemiaEarly Relapse of Acute Myeloid LeukemiaLate Relapse of Acute Myeloid LeukemiaRecurrent Adult Acute Myeloid LeukemiaSecondary Acute Myeloid LeukemiaBlastic Plasmacytoid Dendritic Cell NeoplasmAcute Myeloid LeukemiaAdult Acute Lymphoblastic LeukemiaInterleukin-3 Receptor Subunit Alpha PositiveMinimal Residual DiseaseRefractory Acute Myeloid LeukemiaUntreated Adult Acute Myeloid Leukemia
Interventions
DRUG

cyclophosphamide

Given IV

BIOLOGICAL

Autologous CD123CAR-CD28-CD3zeta-EGFRt-expressing T Lymphocytes

Given IV

OTHER

laboratory biomarker analysis

Correlative studies

BIOLOGICAL

Allogeneic CD123CAR-CD28-CD3zeta-EGFRt-expressing T-lymphocytes

Given IV

DRUG

Fludarabine Phosphate

Given IV

Trial Locations (1)

91010

City of Hope Medical Center, Duarte

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

National Cancer Institute (NCI)

NIH

collaborator

Mustang Bio, Inc.

INDUSTRY

lead

City of Hope Medical Center

OTHER