Table 1.
Study short title | Study identifier | Status | Phase | Condition | Interventional targets | Responsible party | Reference |
Treatment of Relapsed and/or Chemotherapy Refractory CD33 Positive Acute Myeloid Leukemia by CART-33 | NCT01864902 | Unknowna | I/II | rrAML | CD33 | Chinese PLA General Hospital, Beijing, China | Wang et al., 2015 |
CLL1-CD33 cCAR in Patients With Relapsed and/or Refractory, High Risk Hematologic Malignancies | NCT03795779 | Recruiting | Early phase 1 | rrAML | CD33, CLL-1 | iCell Gene Therapeutics, Stony Brook, New York, United States | Liu et al., 2018, 2020 |
Multiple CAR-T Cell Therapy Targeting AML | NCT04010877 | Recruiting | I/II | rrAML | CD33, CLL-1, CD123 | Shenzhen Geno-Immune Medical Institute, Shenzhen, Guangdong, China | Zhang et al., 2020, 2021? |
CD123 Redirected Autologous T Cells for AML | NCT02623582 | Terminated | Early phase 1 | rrAML | CD123 | Abramson Cancer Center of the University of Pennsylvania, Philadelphia, Pennsylvania, United States | Cummins et al., 2017 |
Genetically Modified T-cell Immunotherapy in Treating Patients With Relapsed/Refractory Acute Myeloid Leukemia and Persistent/Recurrent Blastic Plasmacytoid Dendritic Cell Neoplasm | NCT02159495 | Recruiting | I | prBPDCN, rrAML | CD123 | City of Hope Medical Center, Duarte, California, United States | Budde et al., 2018 |
Phase I Study of UCART123 in Patient With Adverse Genetic Risk Acute Myeloid Leukemia | NCT04106076 | Withdrawn | I | AML | CD123 | Cellectis S.A., Paris, France | Cummins and Gill, 2019 |
Study Evaluating Safety and Efficacy of UCART123 in Patients With Relapsed/Refractory Acute Myeloid Leukemia | NCT03190278 | Recruiting | I | rrAML | CD123 | Cellectis S.A., Paris, France | Roboz et al., 2020 |
Safety Study of Anti Lewis Y Chimeric Antigen Receptor in Myeloma, Acute Myeloid Leukemia or Myelodysplastic Syndrome | NCT01716364 | Unknowna | I | (rr)AML, MDS, MM | Lewis Y | Peter MacCallum Cancer Centre, Melbourne, Australia | Ritchie et al., 2013 |
Safety Study of Chimeric Antigen Receptor Modified T-cells Targeting NKG2D-Ligands | NCT02203825 | Completed | I | AML, MDS-RAEB, MM | NKG2D Ligands | Celyad Oncology SA, New York, New York, United States | Baumeister et al., 2019 |
A Dose Escalation Phase I Study to Assess the Safety and Clinical Activity of Multiple Cancer Indications (THINK) | NCT03018405 | Unknowna | I/II | AML, CRC, EOC, FTC, MDS, MM, PC, TCC, TNBC | NKG2D Ligands | Celyad Oncology SA, New York, New York, United States | Sallman et al., 2018, 2019 |
DEPLETHINK - LymphoDEPLEtion and THerapeutic Immunotherapy With NKR-2 (DEPLETHINK) | NCT03466320 | Completed | I/II | AML, MDS | NKG2D Ligands | Celyad Oncology SA, New York, New York, United States | Sallman et al., 2020 |
EPITHINK: Epigenetic Drug Treatment and Therapeutic Immunotherapy With NKR-2 | NCT03612739 | Withdrawn | I | AML | NKG2D ligands | Celyad Oncology SA, New York, New York, United States | Sallman et al., 2020 |
Study in Relapsed/Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome Patients to Determine the Recommended Dose of CYAD-02 | NCT04167696 | Recruiting | I | MDS, rrAML | NKG2D ligands | Celyad Oncology SA, New York, New York, United States | Deeren et al. 2020 |
Dose-escalating Trial With UniCAR02-T Cells and CD123 Target Module (TM123) in Patients With Hematologic and Lymphatic Malignancies | NCT04230265 | Recruiting | I | AML, B-ALL, BPDCN | CD123 | CPT Cellex Patient Treatment GmbH, Dresden, Germany | Wermke et al., 2021 |
As referenced on clinicaltrials.gov.
AML, acute myeloid leukemia; B-ALL, B-Cell Acute Lymphoblastic Leukemia; BPDCN, Blastic Plasmacytoid Dendritic-Cell Neoplasia; CRC, Colorectal Cancer; EOC, Epithelial Ovarian Cancer; FTC, Fallopial Tube Carcinoma; MDS, Myelodysplastic Syndrome; MM, Multiple Myeloma; PC, Prostate Cancer; RAEB, Refractory Anaemia with Excessive Blasts; rrAML, relapsed refractory AML; TCC, Transitional Cell Carcinoma; TNBC, Triple-Negative Breast Cancer.