Drug intelligence / Profile preview

ASAK-22

Development stage
Preclinical
Lead developer
Beijing Institute of Pharmacology and Toxicology
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous, Parenteral
01

Overview

ASAK-22 is a preclinical **antibody-antibiotic conjugate** designed to eradicate intracellular *Staphylococcus aureus*, especially methicillin-resistant *S. aureus* (MRSA). It consists of an anti-*S. aureus* antibody conjugated through a valine-alanine dipeptide linker to the antibiotic payload KRM-1657. The intended mechanism is targeted binding to *S. aureus*, cellular uptake of the conjugate into infected host cells, intracellular linker cleavage, and release of KRM-1657 to kill intracellular bacteria that are poorly cleared by standard extracellularly active antibiotics such as vancomycin. Publicly available evidence for ASAK-22 currently appears limited to a 2024 peer-reviewed preclinical publication reporting in vitro activity against intracellular MRSA and reduced bacterial burden in a mouse bacteremia model after a single administration.

02

Targets

rpoB (DNA-directed RNA polymerase subunit beta)

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