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. 2022 Dec 30;15(1):253. doi: 10.3390/cancers15010253

Table 1.

Published results of clinical trials of bispecific antibodies in AML.

Target Agent Phase Disease Outcome NCT ID
BiTE CD33 × CD3 AMG330 I R/R AML CR+CRi:19% NCT02520427
CRS:67%
CD33 × CD3 AMV564 I R/R AML CR+CRi:66.7% NCT03144245
CRS:5.7%
CD33 × CD3HLE AMG673 I R/R AML Blast reduction:44% NCT03224819
CRS:50%
CD123 × CD3 APVO436 I R/R AML Blast reduction: 7% NCT03647800
CRS:18%
CD123 × CD3 XmAb14045 I R/R AML CR+CRi:14% NCT02730312
(Vibecotamab) CRS:59%
DART CD123 × CD3 Flotetuzumab I/II R/R AML CR/CRi:27% NCT02152956
CRS13%
TRiKE CD33 × CD16 × IL15 1-GBT-3550 I PIF R/R AML SD:50%; POD:25% NCT03214666
No toxicity

BiTE: bispecific T-cell engager; DART: Dual-affinity Re-Targeting Molecules (BiTE); HLE: half-life extended; TRiKE: tri-specific killer engager; R/R: relapsed/refractory; CR: complete remission; CRi: complete remission with incomplete hematologic recovery; SD: stable disease: POD: progression of disease; PIF: primary induction failure; CRS: cytokine-release syndrome.