MedPath

Erenumab

Generic Name
Erenumab
Brand Names
Aimovig
Drug Type
Biotech
CAS Number
1582205-90-0
Unique Ingredient Identifier
I5I8VB78VT

Overview

Erenumab (AMG-334) (INN; trade name Aimovig) is a human monoclonal antibody designed specifically to bind and antagonize the calcitonin gene-related peptide receptor (CGRPR) as a means to prevent migraines. Aimovig, as released and marketed by Novartis and Amgen, is in fact a novel therapeutic approach as the first and only FDA approved treatment specifically developed to prevent migraine by blocking the CGRP receptor, which is believed to play a critical role in migraine . In particular, erenumab-aooe is a human immunoglobulin G2 monoclonal antibody that has high affinity binding to the CGRP receptor . The antibody is produced utlilizing recombinant DNA technology in Chinese hamster ovary cells . It is composed of 2 heavy chains, each containing 456 amino acids, and 2 light chains of the lambda subclass, each containing 216 amino acids, with an approximate molecular weight of 150 kDa .

Background

Erenumab (AMG-334) (INN; trade name Aimovig) is a human monoclonal antibody designed specifically to bind and antagonize the calcitonin gene-related peptide receptor (CGRPR) as a means to prevent migraines. Aimovig, as released and marketed by Novartis and Amgen, is in fact a novel therapeutic approach as the first and only FDA approved treatment specifically developed to prevent migraine by blocking the CGRP receptor, which is believed to play a critical role in migraine . In particular, erenumab-aooe is a human immunoglobulin G2 monoclonal antibody that has high affinity binding to the CGRP receptor . The antibody is produced utlilizing recombinant DNA technology in Chinese hamster ovary cells . It is composed of 2 heavy chains, each containing 456 amino acids, and 2 light chains of the lambda subclass, each containing 216 amino acids, with an approximate molecular weight of 150 kDa .

Indication

Erenumab is indicated for the preventative treatment of migraine in adults .

Associated Conditions

  • Migraine

FDA Approved Products

AIMOVIG
Manufacturer:Amgen Inc
Route:SUBCUTANEOUS
Strength:140 mg in 1 mL
Approved: 2023/05/16
NDC:55513-842
AIMOVIG
Manufacturer:Amgen Inc
Route:SUBCUTANEOUS
Strength:70 mg in 1 mL
Approved: 2023/05/16
NDC:55513-840
AIMOVIG
Manufacturer:Amgen Inc
Route:SUBCUTANEOUS
Strength:70 mg in 1 mL
Approved: 2023/05/16
NDC:55513-841
AIMOVIG
Manufacturer:Amgen Inc
Route:SUBCUTANEOUS
Strength:140 mg in 1 mL
Approved: 2023/05/16
NDC:55513-843

Singapore Approved Products

AIMOVIG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE 140MG/ML
Manufacturer:Amgen Manufacturing Limited (Bulk Production/Primary Packaging)
Form:INJECTION, SOLUTION
Strength:140 MG/ML
Online:Yes
Approved: 2020/04/03
Approval:SIN15926P
AIMOVIG SOLUTION FOR INJECTION IN PRE-FILLED PEN 140MG/ML
Manufacturer:Amgen Manufacturing Limited (Bulk Production/Primary Packaging)
Form:INJECTION, SOLUTION
Strength:140 MG/ML
Online:Yes
Approved: 2020/04/03
Approval:SIN15925P
AIMOVIG SOLUTION FOR INJECTION IN PRE-FILLED PEN 70MG/ML
Manufacturer:Amgen Manufacturing Limited (Bulk Production/Primary Packaging)
Form:INJECTION, SOLUTION
Strength:70mg/ml
Online:Yes
Approved: 2018/09/21
Approval:SIN15543P
AIMOVIG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE 70MG/ML
Manufacturer:Amgen Manufacturing Limited (Bulk Production/Primary Packaging)
Form:INJECTION, SOLUTION
Strength:70mg/ml
Online:Yes
Approved: 2018/09/21
Approval:SIN15545P

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