Drug intelligence / Profile preview

liposomal mitoxantrone hydrochloride + cyclophosphamide + vincristine + prednisone

Development stage
Unknown
Lead developer
CSPC Pharmaceutical Group
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules, Liposomes → Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Allosteric Modulators → Classical Binding Small Molecules → Small Molecules
Administration
Intravenous, Oral
01

Overview

The combination of liposomal mitoxantrone hydrochloride, cyclophosphamide, vincristine, and prednisone—commonly referred to as the CMOP regimen—is an investigational chemotherapy protocol primarily studied for hematologic malignancies such as peripheral T-cell lymphoma (PTCL) and angioimmunoblastic T-cell lymphoma (AITL)[1][2][4][5]. Liposomal mitoxantrone is a novel anthracycline-class antitumor agent formulated in a liposome to improve drug stability, control release kinetics, enhance tumor targeting, and reduce cardiotoxicity compared to conventional anthracyclines[5]. Cyclophosphamide is an alkylating agent that crosslinks DNA; vincristine is a vinca alkaloid that inhibits microtubule formation; and prednisone is a synthetic glucocorticoid with anti-inflammatory and immunosuppressive effects. The combination aims to maximize antitumor efficacy while minimizing adverse effects. Clinical studies have shown promising response rates with manageable toxicity profiles in relapsed/refractory PTCL and AITL patients[1][2][4][5].

Other names
mitoxantrone hydrochloride liposome + cyclophosphamide + vincristine + prednisonemitoxantrone hydrochloride liposome
02

Targets

TUBB (Tubulin (alpha and beta subunits))GR (Glucocorticoid receptor)TOP2A (DNA topoisomerase II)DNA

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