Drug intelligence / Profile preview

mifamurtide

Development stage
Phase 2
Lead developer
Takeda
Modality
Liposomes → Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

Mifamurtide is a synthetic immunomodulator and a derivative of muramyl dipeptide (MDP), formulated as a liposomal preparation. It acts by activating monocytes and macrophages, primarily through interaction with the nucleotide-binding oligomerization domain 2 (NOD2) receptor, leading to nuclear factor kappa B (NF-kB) activation. This results in the production of proinflammatory cytokines and enhances both bactericidal and tumoricidal immune responses. Mifamurtide is used as an adjuvant therapy in combination with postoperative multi-agent chemotherapy for high-grade, resectable, non-metastatic osteosarcoma after complete surgical resection in children, adolescents, and young adults. The drug has demonstrated improved overall survival when added to standard chemotherapy regimens[1][2][3][4][5][8].

Brand names
MepactJunovan
Other names
mifamurtide sodium hydratesodium mifamurtidemuramyl tripeptide PEmuramylNAc-Ala-isoGln-Lys-tripeptide-PE
02

Targets

TLR4 (Toll-like receptor 4)NOD2 (Nucleotide-binding oligomerization domain-containing protein 2)

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