Erenumab (AMG 334) is the first human
monoclonal antibody antagonist against the Calcitonin Gene-Related Peptide
Receptor (CGRP) receptor. Like the small-molecule CGRP-receptor antagonists, Erenumab
fully antagonizes CGRP-receptor function and is dose-dependently effective in
an in vivo target coverage model that
exhibits translatability to humans.
Erenumab
fully inhibited CGRP-stimulated cAMP production with an IC50 of 2.3
nM in cell-based functional assays (human CGRP receptor) and was 5000-fold more
selective for the CGRP receptor than other human calcitonin family receptors,
including adrenomedullin, calcitonin, and amylin receptors.
Erenumab is currently in clinical development for the prevention of
migraine. On 21st June 2017, Novartis announced that the European Medicines
Agency (EMA) has accepted its Marketing Authorization Application (MAA) for Erenumab
in the prevention of migraines.
Calcitonin Gene-Related Peptide (CGRP) as a
Target for Migraines Treatment
Migraine
is a distinct neurological disease which involves recurrent attacks of moderate
to severe head pain that is typically pulsating, often unilateral and
associated with nausea, vomiting and sensitivity to light, sound and odors.
Migraine
has a profound and limiting impact on an individual’s abilities to carry out
everyday tasks, and was declared by the World Health Organization (WHO) to be
one of the top 10 causes of years lived with disability for men and women. It
remains under-recognized, under-treated, associated with disability, reduced
quality of life, and financial cost to society.
Existing
preventive therapies have been repurposed from other indications and are often
associated with poor tolerability and lack of efficacy, which leads to increasing
discontinuation rates and dissatisfaction among patients. The cause and
triggers of migraine are not fully understood as no two migraines are the same.
Calcitonin
gene-related peptide (CGRP) is a 37-aminoacid-long peptide expressed in both
the central and peripheral nervous systems. CGRP belongs to the calcitonin
family of peptides that also consists of adrenomedullin, calcitonin, and
amylin, all of which have important physiologic functions: adrenomedullin is a
potent vasodilator, causes prolactin release, and plays a role in diuresis and
food intake; calcitonin is involved in the control of bone metabolism; and
amylin is thought to be a gut-brain axis hormone that improves glucose
metabolism, acts as a trophic factor to promote cell growth, and modulates
inflammation.
CGRP is
one of the most potent vasodilators discovered to date. It also plays a role in
a variety of other activities, including modulation of nociception and
neurogenic inflammation. Several lines of evidence suggest a role for CGRP in
migraine pathogenesis:
A: Elevated
levels of CGRP have been detected in individuals with migraine.
B: Intravenous
CGRP infusion produces lasting headaches in healthy individuals and migraine
headache in migraineurs.
Most importantly, several small-molecule CGRP-receptor antagonists have shown clinical efficacy in acute migraine and in migraine prevention.
Complete PDF file is available on request.
Most importantly, several small-molecule CGRP-receptor antagonists have shown clinical efficacy in acute migraine and in migraine prevention.
Complete PDF file is available on request.