Drug intelligence / Profile preview

MIC12

Development stage
Preclinical
Lead developer
University Hospital Tübingen
Modality
Immunomodulatory ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes, Cytokines & Interferons → Recombinant Proteins and Enzymes, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

MIC12 is a novel, target-restricted immunocytokine developed for the treatment of acute myeloid leukemia (AML). It consists of a humanized monoclonal antibody targeting CLEC12A (CLL-1) with an Fc-optimized domain (containing S239D and I332E mutations, known as SDIE) fused to a modified interleukin-15 (IL-15) moiety. The IL-15 component features an E46K mutation that abrogates its binding to the IL-15Rα chain, thereby ensuring that its stimulatory activity is conditionally activated only upon binding to the CLEC12A antigen on target cells. This design allows for the localized stimulation of IL-15Rβ/γ-expressing effector cells, such as natural killer (NK) cells, while minimizing systemic off-target toxicity. Developed through a collaboration between ABL Bio and the University of Tübingen, MIC12 has demonstrated superior NK cell activation, proliferation, and anti-leukemic efficacy in preclinical models compared to standard Fc-optimized antibodies.

Other names
CLEC12A-directed immunocytokineCLEC-12A-directed immunocytokineCLEC 12A-directed immunocytokineanti-CLEC12A IL-15 immunocytokineanti-CLEC-12A IL-15 immunocytokineanti-CLEC 12A IL-15 immunocytokineCLL-1-directed immunocytokineCLL1-directed immunocytokineCLL 1-directed immunocytokine
02

Targets

CLEC12AIL15RA (Interleukin-15 receptor subunit alpha)IL2RB (IL-2 receptor beta chain)IL2RG (Interleukin-2 receptor gamma subunit)FCGR3A (Low affinity immunoglobulin gamma Fc region receptor III-A)

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