Drug intelligence / Profile preview

plovamer acetate

Development stage
Phase 2
Lead developer
EMD Serono
Modality
Peptides, Small Molecules
Administration
Subcutaneous Injection[7]
01

Overview

Plovamer acetate is a second-generation synthetic random copolymer of four amino acids (L-glutamic acid, L-alanine, L-tyrosine, and L-lysine) designed as an immunomodulatory peptide for the treatment of autoimmune diseases. It was rationally engineered to improve upon glatiramer acetate by optimizing the ratio and sequence of its constituent amino acids. Plovamer acetate acts primarily as a major histocompatibility complex (MHC) class II modulator; it competitively binds to MHC II with higher affinity than glatiramer acetate and induces a T-helper 2 (Th2)-like immune response. This mechanism is intended to reduce inflammatory activity in diseases such as multiple sclerosis by shifting immune responses away from pro-inflammatory pathways. The drug was developed by Peptimmune and EMD Serono for indications including relapsing-remitting multiple sclerosis (RRMS), Crohn's disease, rheumatoid arthritis, and uveitis but development has been discontinued in all indications[2][3][7].

Other names
plovamerPI-2301PI2301PI 2301CO-14CO14CO 14
02

Targets

MHC II (Major histocompatibility complex class II receptor)

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