Drug intelligence / Profile preview

glatiramer acetate + mitoxantrone

Development stage
Phase 2
Lead developer
Teva Pharmaceutical Industries
Modality
Small Molecules
Administration
Subcutaneous, Intravenous
01

Overview

Glatiramer acetate + mitoxantrone is a combination of two drugs used in the management of multiple sclerosis (MS). Glatiramer acetate is a synthetic mixture of polypeptides composed of L-glutamic acid, L-alanine, L-tyrosine, and L-lysine. It acts as an immunomodulator by binding to major histocompatibility complex (MHC) class II molecules on antigen-presenting cells, preventing myelin basic protein from stimulating these cells. This shifts the immune response from pro-inflammatory to anti-inflammatory and induces regulatory T cells that suppress MS activity[1][2][6]. Mitoxantrone is an antineoplastic agent with immunosuppressive properties; it intercalates into DNA and inhibits topoisomerase II, leading to suppression of B-cell, T-cell, and macrophage function. Mitoxantrone reduces relapse rates and delays disability progression in secondary progressive MS but has limitations due to potential cardiotoxicity[5]. The combination may be considered for certain patients with aggressive or refractory forms of MS.

Other names
GA (for glatiramer acetate)
02

Targets

MHC II (Major histocompatibility complex class II receptor)γδ TCR (T-cell receptor)TOP2A (DNA topoisomerase II)

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