Drug intelligence / Profile preview

alemtuzumab

Development stage
Approved
Lead developer
Sanofi
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Subcutaneous
01

Overview

Alemtuzumab is a humanized IgG1 kappa monoclonal antibody that targets the cell surface glycoprotein CD52, which is present on T and B lymphocytes, natural killer cells, monocytes, and macrophages. It is used primarily for the treatment of B-cell chronic lymphocytic leukemia (B‑CLL) and relapsing forms of multiple sclerosis (MS). The drug works by binding to CD52 on lymphocytes and inducing antibody-dependent cellular cytolysis and complement-mediated lysis. This results in rapid depletion of circulating T and B cells followed by gradual repopulation with altered immune cell subsets. Alemtuzumab was developed from the original rat-derived Campath antibodies at Cambridge University; it was later humanized to reduce immunogenicity. It is marketed as Lemtrada for MS and as Campath or MabCampath for B‑CLL[1][2][10].

Brand names
CampathLemtradaMabCampath
Other names
Monoclonal Antibody Campath-1HImmunoglobulin G 1 (human-rat monoclonal CAMPATH-1H gamma1-chain anti-human antigen CD52), disulfide with human-rat monoclonal CAMPATH-1H light chain, dimer
02

Targets

CD52 (CD52 Antigen)

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