Drug intelligence / Profile preview

Timexon

Development stage
Phase 3
Lead developer
Biocad
Modality
Peptides
Administration
Subcutaneous
01

Overview

Timexon is an immunomodulating medication consisting of the acetate salts of synthetic polypeptides containing four naturally occurring amino acids: L-glutamic acid, L-alanine, L-tyrosine, and L-lysine. Developed by Biocad, it is a generic version of the reference drug Copaxone. Timexon is indicated for the treatment of relapsing-remitting multiple sclerosis (RRMS) to reduce the frequency of relapses. Its mechanism involves shifting the immune response from pro-inflammatory Th1 T-cells to regulatory, anti-inflammatory Th2 T-cells that migrate to the central nervous system and suppress local inflammation. Additionally, it acts as a decoy by competing with myelin antigens for binding to major histocompatibility complex (MHC) class II molecules, thereby inhibiting the activation of myelin-reactive T-cells.

Brand names
Timexon
Other names
glatiramer acetateBCD-063BCD063BCD 063
02

Targets

γδ TCR (T-cell receptor)

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