Drug intelligence / Profile preview

olverembatinib + blinatumomab + chidamide

Development stage
Unknown
Lead developer
Ascentage Pharma
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

The ABC regimen is an experimental, chemotherapy-free combination therapy being evaluated for the treatment of newly diagnosed Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL). This triplet regimen consists of **olverembatinib** (a third-generation BCR-ABL1 tyrosine kinase inhibitor), **blinatumomab** (a CD3/CD19 bispecific T-cell engager), and **chidamide** (a subtype-selective histone deacetylase inhibitor). Olverembatinib is designed to overcome resistance mutations, including the T315I mutation, which often confers resistance to earlier-generation TKIs. Blinatumomab facilitates a T-cell-mediated immune response against CD19-expressing leukemia cells, while chidamide acts as an epigenetic modulator to potentially enhance the efficacy of the other agents and overcome further resistance mechanisms. The regimen is being studied primarily by researchers at Nanfang Hospital, Southern Medical University, as a first-line treatment option for patients, including those ineligible for allogeneic hematopoietic stem cell transplantation.

Brand names
Olverembat + Blincyto + Epidaza
Other names
ABC study regimenOlverembatinib, Blinatumomab, and Chidamide combination
02

Targets

CD19 (B lymphocyte antigen CD19)KIT (c-KIT proto-oncogene receptor tyrosine kinase)HDAC10 (Histone Deacetylase 10)HDAC1 (Histone Deacetylase 1)ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase)CD3 (T-cell surface glycoprotein CD3)

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