Erenumab
Introduction to Erenumab
Erenumab (brand name: Aimovig) is a fully human monoclonal antibody that belongs to the class of calcitonin gene-related peptide (CGRP) receptor antagonists. It was approved by the FDA in 2018 for the preventive treatment of migraine in adults. Erenumab represents a significant advance in migraine therapy, offering a targeted approach to migraine prevention.
Mechanism of Action
Erenumab works by:
- Selectively binding to the CGRP receptor
- Blocking the biological activity of CGRP, a neuropeptide involved in migraine pathophysiology
- Inhibiting CGRP-mediated vasodilation and neurogenic inflammation
- Preventing CGRP-induced sensitization of trigeminal neurons
Indications
Erenumab is primarily indicated for:
- Preventive treatment of migraine in adults
- Both episodic and chronic migraine
Dosage and Administration
- Available in pre-filled autoinjector pens
- Recommended dosage: 70 mg once monthly; some patients may benefit from 140 mg once monthly
- Administered subcutaneously
- Can be self-administered by patients after proper training
- No dose adjustment required for renal or hepatic impairment
Efficacy
Clinical trials have demonstrated significant efficacy:
- Reduction in monthly migraine days by 3-4 days compared to placebo
- 50% or greater reduction in monthly migraine days in about 40-50% of patients
- Improvement in quality of life and disability scores
- Onset of efficacy observed as early as the first month of treatment
- Sustained efficacy demonstrated in long-term studies (up to 5 years)
Safety and Adverse Effects
Erenumab is generally well-tolerated. Common adverse effects include:
- Injection site reactions (pain, erythema, pruritus)
- Constipation
- Muscle spasms
- Mild to moderate upper respiratory tract infections
- Hypersensitivity reactions
- Hypertension
- Cardiovascular effects (theoretical risk based on CGRP's vasodilatory properties)
Pediatric Considerations
While Erenumab is not currently approved for use in pediatric populations:
- Clinical trials in adolescents (12-17 years) are ongoing
- Preliminary data suggests a similar safety profile to adults
- Efficacy in pediatric populations is still being evaluated
- Off-label use in refractory cases has been reported in literature, but more research is needed
- Pediatricians should closely monitor ongoing research and guidelines for potential future use in pediatric migraine prevention