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. 2022 Sep 12;18(6):2114254. doi: 10.1080/21645515.2022.2114254

Table 4.

Some major ongoing clinical trials on CAR T-cell therapy in blood and solid cancers.

Clinical trial Target Cancer type Phase Updated result/status
Hematological malignancies
NCT03277729 CD20 R/R B-NHL Phase 1/2 High overall and complete response with an extremely favorable safety profile in B-NHL.188
NCT03262298 CD22 R/R B-ALL Phase 1/2 Dose-dependent antileukemic activity was observed by targeting CD22 in B-ALL.182
NCT02690545, NCT02917083) CD30 R/R HL Phase 1/2 It shows an ORR of 72% and a CR rate of 59% in R/R HL with an excellent safety profile.118
NCT02203825 NKG2D R/R AML Phase 1 Targeting NKG2D-Ligands observed to result in high efficacy against AML.189
NCT03971799 CD33 R/R AML phase 1/2 Recruiting
NCT04014881 CD123 R/R AML Phase 1 Recruiting
NCT04010877 CLL-1/CD123/CD33 R/R AML Phase 1/2 Recruiting
NCT05023707 FLT3 R/R AML Phase 1/2 The potent In vitro antitumor activities of Flt3-CAR T-cells, combined with their low off-target cytotoxicity, offer hope in the treatment of AML.190
NCT02842320 IL-1RAP CML   CAR T-cell therapy exhibited cytotoxicity against leukemic cells expressing IL-1RAP.191
NCT04689659 CD7 R/R T- ALL Phase 1/2 Phase 1 trial indicated CD7-targeted CAR T-cells result in efficient expansion and achieved a high CR rate with manageable safety profiles.183
NCT02203825 NKG2D R/R T-ALL, AML, MDS, MM Phase 1 Targeting NKG2D-Ligands shows robust efficacy against T-ALL.189
NCT04351022 CD38 R/R AML Phase 1/2 66.7% patient achieved CR with OS of 7.9 months.192
NCT03081910 CD5 R/R T-NHL Phase 1 CD5 CAR T-cells are safe and can induce clinical responses in heavily treated patients with R/R CD5+ T-NHL.193
NCT04712864 CD4 R/R T-cell lymphoma Phase 1 CD4CART-cells have potent cytotoxic effects on T-cell lymphoma.194
NCT04594135 CD5 T-ALL Phase 1 CD5 CAR T-cells eradicate T-ALL blasts In vitro and control disease progression in xenograft mouse models of T-ALL.195
Solid malignancies
NCT03500991 HER2 CNS tumor Phase 1 HER2-specific CAR T-cells is well tolerated and activate a localized immune response in pediatric and young adult patients.196
NCT03618381 EGFR806 Advanced solid cancers Phase 1 Recruiting
NCT03525782 MUC1/PD-1 NSCLC Phase 1/2 Recruiting
NCT03198052 PSCA/MUC1/TGFβ, HER2/Mesothelin, Lewis-Y/GPC3/AXL/EGFR, Claudin18.2/B7H3 Lung cancer Phase 1 Recruiting
NCT04099797 GD2 Brain cancer Phase 1 Recruiting
NCT02932956 GPC3 Liver cancer Phase 1 Active but not recruiting
NCT01583686 Mesothelin Ovarian, cervical, pancreatic, lung cancer Phase 1/2 Recruiting
NCT02349724 CEA Lung, colorectal, gastric, breast, pancreatic cancer Phase 1 Recruiting
NCT04483778 B7H3, CD19 Advanced solid tumors Phase 1 Recruiting
NCT04025216 TnMUC1 R/R solid cancers Phase 1 Active but not recruiting

Abbreviations: ALL, Acute lymphoblastic leukemia; AML, Acute Myeloid Leukemia; CEA, carcinoembryonic antigen; CLL-1, C-type lectin-like molecule-1; CML, Chronic Myeloid Leukemia; CNS, central nervous system; EGFR, Epidermal growth factor receptor; GPC3, Glypican-3 IL1RAP, HL, Hodgkin’s Lymphoma; IL1 receptor-associated protein; MDS, myelodysplastic syndrome; MM, multiple myeloma; NHL, non-Hodgkin’s Lymphoma; NKG2D, Natural killer group 2D; NSCLC, Non-small cell lung cancer; PSCA, Prostate stem cell antigen