Erenumab is a monoclonal antibody developed for the prevention of migraine, including episodic and chronic forms. Marketed as Aimovig (erenumab), it targets the calcitonin gene-related peptide receptor pathway implicated in migraine pathophysiology. Clinical trials have demonstrated significant reductions in monthly migraine days, improved quality-of-life measures, and sustained efficacy over long-term follow-up. This article reviews erenumab uses, dosing, mechanism of action, safety profile, and emerging evidence.

Erenumab Uses

Erenumab is approved for:

  • Prevention of episodic migraine
  • Prevention of chronic migraine
  • Reduction in monthly migraine days
  • Decreasing reliance on acute rescue medications

It is not indicated for acute migraine treatment. It is a preventive biologic therapy.

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Erenumab Dosage & Administration

Erenumab injection is administered subcutaneously using an autoinjector pen.

Standard Dosing

  • 70 mg once monthly
  • 140 mg once monthly, depending on response

Erenumab dosing may be adjusted based on therapeutic response and tolerability.

There is no erenumab tablet formulation. The drug is available only as a subcutaneous injection.

Erenumab administration is designed for self-injection after clinical instruction.

How Erenumab Works?

Development, Pharmacokinetics and Pharmacodynamics of Erenumab

Erenumab is a fully human monoclonal antibody targeting the CGRP receptor. After subcutaneous injection:

  • Peak plasma concentration occurs in approximately 4 to 6 days
  • Effective half-life is approximately 28 days
  • Monthly administration maintains steady-state levels

Pharmacodynamically, erenumab blocks receptor activation without crossing the blood-brain barrier extensively.

Erenumab Mechanism of Action

Migraine pathophysiology involves activation of the trigeminovascular system and release of CGRP, a potent vasodilator and pain mediator.

Erenumab mechanism of action involves:

  • Binding to the CGRP receptor
  • Preventing CGRP from activating downstream inflammatory and nociceptive pathways
  • Reducing neurogenic inflammation
  • Decreasing migraine frequency

Unlike small-molecule CGRP antagonists, erenumab specifically targets the receptor rather than the peptide.

Role of Erenumab in the Treatment of Migraine

Migraine remains a leading cause of disability globally. Traditional preventive treatments include beta-blockers, anticonvulsants, and antidepressants, many with systemic adverse effects.

Erenumab represents a targeted biologic approach.

It is particularly useful in:

  • Patients with inadequate response to oral preventives
  • Chronic migraine cases
  • Patients intolerant to conventional therapies

Erenumab: Clinical Data in Migraine

Multiple phase II and III erenumab clinical trials evaluated efficacy in episodic and chronic migraine populations.

Key findings include:

  • Reduction of 3 to 4 monthly migraine days in episodic migraine
  • Reduction of 6 to 7 monthly migraine days in chronic migraine
  • Sustained response in long-term extension studies
  • Improvement in patient-reported disability scales

The APPRAISE study erenumab and other real-world studies have reinforced its safety and effectiveness in routine practice.

Migraine-Related Disability and Quality of Life Scales in Erenumab Trials

Clinical trials utilized:

  • MIDAS (Migraine Disability Assessment)
  • HIT-6 (Headache Impact Test)
  • MSQ (Migraine-Specific Quality of Life Questionnaire)

Results showed statistically significant improvements compared to placebo groups.

Common Side Effects of Erenumab

Side Effects

Search queries around erenumab side effects and erenumab injection side effects are common.

Reported adverse effects include:

  • Injection site reactions
  • Constipation
  • Muscle cramps
  • Rare hypersensitivity reactions

Drug–Drug Interactions

Erenumab has minimal known drug–drug interactions due to its monoclonal antibody structure and lack of hepatic metabolism via cytochrome P450 pathways.

Safety and Tolerability of Erenumab

Long-term safety data show:

  • Stable adverse event rates over time
  • Low discontinuation rates
  • Minimal cardiovascular safety signals

However, post-marketing surveillance continues to evaluate rare events.

Limitations in the Use of Erenumab

Despite clinical benefits, limitations include:

  • Cost considerations
  • Insurance coverage variability
  • Injection route preference barriers
  • Limited long-term data beyond five years

Questions regarding erenumab rosacea, hair loss, and rare dermatologic effects remain under observation.

Erenumab: Future Directions

Emerging research is exploring:

  • Combination therapy strategies
  • Predictive biomarkers for response
  • Real-world effectiveness data
  • Long-term cardiovascular outcomes

List of Studies & Clinical Trials So Far

Major trials include:

  • ARISE trial
  • STRIVE trial
  • LIBERTY trial
  • Long-term open-label extension studies

These collectively demonstrate significant migraine day reduction and sustained tolerability.

Conclusions

Erenumab represents a targeted, receptor-specific preventive therapy for migraine. By inhibiting the CGRP receptor pathway, it reduces migraine frequency and disability with a favorable tolerability profile. As clinical data accumulates, erenumab continues to shape modern migraine prevention strategies.

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Frequently Asked Questions

What is the success rate of erenumab?

Clinical trials report that approximately 40 to 50 percent of patients achieve at least a 50 percent reduction in monthly migraine days, depending on migraine subtype.

How long does it take for erenumab to work?

Some patients report improvement within the first month. Full therapeutic evaluation is typically assessed after three months.

How long does erenumab last?

Each injection lasts approximately one month. The half-life supports monthly dosing.

Does erenumab cause hair loss?

Hair loss is not a commonly reported adverse effect in major clinical trials. Post-marketing data continue to monitor rare events.

What is the best medication for chronic migraines?

Treatment depends on patient profile. Options include CGRP inhibitors such as erenumab, onabotulinumtoxinA, and traditional oral preventives. Clinical evaluation is required.