Drug intelligence / Profile preview

IMD2128

Development stage
Preclinical
Lead developer
Affinity Biopharmaceutical
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

IMD2128 is a bispecific antibody-drug conjugate (ADC) targeting the epidermal growth factor receptor (EGFR) and c-Met (hepatocyte growth factor receptor). Developed by Affinity Biopharmaceutical, it utilizes the TMEAlinker platform, which is a tumor microenvironment (TME)-activated linker specifically cleaved by extracellular legumain. The ADC carries an eribulin payload with a drug-to-antibody ratio (DAR) of 2. In preclinical studies, IMD2128 has demonstrated potent antitumor activity in lung and pancreatic carcinoma models, including those resistant to DXd-based ADCs. It exhibits high plasma stability and a favorable safety profile in non-human primates, with a highest non-severely toxic dose (HNSTD) over 16 mg/kg in cynomolgus monkeys.

02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)MET (Mesenchymal-epithelial transition factor receptor)TUBB (Tubulin (alpha and beta subunits))

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