Table 3.

Non-FDA-approved CAR T-cell therapies with complete clinical trial data available

Allo-715MCARH109Xuzhou GPRC5D CAR T cell therapyOriCAR-017
Trial phase 
Target BCMA GPRC5D GPRC5D GPRC5D 
Specificity Allogeneic Autologous Autologous Autologous 
Patients enrolled (infused) 48 (43) 19 (17) 33 (33) 13 (10)* 
Median age (range), y 64 (46-77) 60 (38-76) 58 (39-70) 64 (58-68) 
Median prior lines (range) 5 (3-11) 6 (4-14) 4 (2-12) 5.5 (4-10) 
Triple-class refractory, No. (%) 39 (91) 16 (94) Not reported Not reported 
Penta refractory, No. (%) 18 (42) Not reported Not reported Not reported 
Prior anti-BCMA CAR T-cell therapy, No. (%) Excluded 8 (47) 9 (27) 5 (50) 
Received bridging therapy, No. (%) 16 (94) Not reported 2 (80) 
ORR, No. (%) 24 (56) 12 (71) 30 (91) 10 (100) 
CR, No. (%) Not reported 6 (35) 21 (64) 6 (60) 
ORR in patients with prior anti-BCMA CAR T-cell therapy, No. (%)  7/10 (70) 9/9 (100) 5 (100) 
Median PFS Not reported Not reached Not reached Not reached 
CRS grade 3+, No. (%) 1 (2) 1 (6) 0 (0) 0 (0) 
ICANS grade 3+, No. (%) 0 (0) 1 (6) 1 (3) 0 (0) 
Trial ID NCT04093596 NCT04555551 ChiCTR2100048888 NCT05016778 
Allo-715MCARH109Xuzhou GPRC5D CAR T cell therapyOriCAR-017
Trial phase 
Target BCMA GPRC5D GPRC5D GPRC5D 
Specificity Allogeneic Autologous Autologous Autologous 
Patients enrolled (infused) 48 (43) 19 (17) 33 (33) 13 (10)* 
Median age (range), y 64 (46-77) 60 (38-76) 58 (39-70) 64 (58-68) 
Median prior lines (range) 5 (3-11) 6 (4-14) 4 (2-12) 5.5 (4-10) 
Triple-class refractory, No. (%) 39 (91) 16 (94) Not reported Not reported 
Penta refractory, No. (%) 18 (42) Not reported Not reported Not reported 
Prior anti-BCMA CAR T-cell therapy, No. (%) Excluded 8 (47) 9 (27) 5 (50) 
Received bridging therapy, No. (%) 16 (94) Not reported 2 (80) 
ORR, No. (%) 24 (56) 12 (71) 30 (91) 10 (100) 
CR, No. (%) Not reported 6 (35) 21 (64) 6 (60) 
ORR in patients with prior anti-BCMA CAR T-cell therapy, No. (%)  7/10 (70) 9/9 (100) 5 (100) 
Median PFS Not reported Not reached Not reached Not reached 
CRS grade 3+, No. (%) 1 (2) 1 (6) 0 (0) 0 (0) 
ICANS grade 3+, No. (%) 0 (0) 1 (6) 1 (3) 0 (0) 
Trial ID NCT04093596 NCT04555551 ChiCTR2100048888 NCT05016778 
*

Thirteen patients were screened for the trial, but 1 was excluded due to low plasma cell GPRC5D expression.

Values listed are for only the enrolled patients receiving product infusion.

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