Drug intelligence / Profile preview

MAb52-4.2-ADC

Development stage
Preclinical
Lead developer
MedAbome
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intraperitoneal
01

Overview

MAb52-4.2-ADC is a first-in-class antibody-drug conjugate (ADC) targeting SLC3A2 (also known as CD98 heavy chain or 4F2hc), a transmembrane glycoprotein overexpressed in various solid and hematologic malignancies. Developed by MedAbome, Inc., the drug consists of a humanized monoclonal antibody (MAb52-4.2) that selectively recognizes a tumor-associated conformational epitope of SLC3A2. This antibody is conjugated to the cytotoxic payload monomethyl auristatin E (MMAE) via a protease-cleavable MC-Vc-PAB linker, with a drug-to-antibody ratio (DAR) of 4. In preclinical studies, MAb52-4.2-ADC demonstrated potent anti-proliferative activity and significant tumor regression in xenograft models of triple-negative breast cancer (TNBC), non-small cell lung cancer (NSCLC), and gastric cancer, while showing minimal cross-reactivity with normal tissues.

Other names
anti-SLC3A2 ADCanti-SLC-3A2 ADCanti-SLC 3A2 ADC
02

Targets

SLC3A2 (Solute carrier family 3 member 2)TUBB (Tubulin (alpha and beta subunits))

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