Aimovig (erenumab) vs Ubrelvy (ubrogepant)

Aimovig (erenumab) vs Ubrelvy (ubrogepant)

Aimovig (erenumab) is a preventative medication for migraines, administered monthly via injection, and works by blocking the calcitonin gene-related peptide (CGRP) receptor, which plays a key role in migraine development. Ubrelvy (ubrogepant), on the other hand, is an oral medication taken as needed when a migraine occurs and belongs to a class of drugs called CGRP receptor antagonists that block the effects of CGRP during a migraine attack. When deciding between the two, Aimovig is typically chosen for ongoing migraine prevention, while Ubrelvy is used for the acute treatment of migraine symptoms as they arise.

Difference between Aimovig and Ubrelvy

Metric Aimovig (erenumab) Ubrelvy (ubrogepant)
Generic name Erenumab Ubrogepant
Indications Preventive treatment of migraine in adults Acute treatment of migraine with or without aura in adults
Mechanism of action Calcitonin gene-related peptide receptor (CGRP) antagonist Calcitonin gene-related peptide receptor (CGRP) antagonist
Brand names Aimovig Ubrelvy
Administrative route Subcutaneous injection Oral
Side effects Injection site reactions, constipation, muscle spasms, etc. Nausea, somnolence, dry mouth, etc.
Contraindications Known hypersensitivity to erenumab or any of its excipients Known hypersensitivity to ubrogepant or any of its excipients
Drug class Monoclonal antibody Small molecule CGRP receptor antagonist
Manufacturer Amgen Allergan

Efficacy

Efficacy of Aimovig (Erenumab) for Migraine Prevention

Aimovig (erenumab) is a novel therapeutic agent designed specifically for the prevention of migraine. It is a monoclonal antibody that targets the calcitonin gene-related peptide (CGRP) receptor, which is believed to play a critical role in migraine pathophysiology. Clinical trials have demonstrated that Aimovig can reduce the number of monthly migraine days in individuals with episodic and chronic migraine. Patients treated with Aimovig reported experiencing at least a 50% reduction in the number of migraine days per month, which signifies a substantial improvement in the burden of the disease. The efficacy of Aimovig has been observed to be consistent across a broad range of patients, including those who have previously failed to respond to other preventive treatments.

Efficacy of Ubrelvy (Ubrogepant) for Acute Migraine Treatment

Ubrelvy (ubrogepant) is an oral medication approved for the acute treatment of migraine with or without aura in adults. As a CGRP receptor antagonist, Ubrelvy works by blocking the activity of CGRP, which is released during a migraine attack and is associated with pain signaling. In clinical studies, Ubrelvy has been shown to be effective in relieving migraine pain and the most bothersome symptom (such as nausea, light sensitivity, or sound sensitivity) within two hours after taking the dose. A significant percentage of patients treated with Ubrelvy experienced pain freedom and absence of their most bothersome symptom, indicating the drug's efficacy in treating migraine attacks.

Comparison of Aimovig and Ubrelvy in Migraine Management

While both Aimovig and Ubrelvy target the CGRP pathway, their roles in migraine management are distinct. Aimovig is used as a preventive treatment, aimed at reducing the frequency of migraine attacks before they start. In contrast, Ubrelvy is utilized as an acute treatment, intended to alleviate the pain and symptoms once a migraine attack has begun. The choice between these medications depends on the patient's specific needs, whether it is prevention or acute relief. Some patients might benefit from using both medications in conjunction to manage their migraines more effectively.

Considerations and Patient Response

It is important to note that individual response to migraine medications can vary. While Aimovig and Ubrelvy have shown efficacy in clinical trials, not all patients will experience the same level of benefit. Factors such as the frequency and severity of migraine attacks, previous treatment history, and the presence of comorbidities can influence the effectiveness of these medications. Patients should discuss with their healthcare provider the most appropriate treatment options based on their specific condition and medical history. Additionally, the long-term safety and efficacy of these treatments are continually being monitored and evaluated through post-marketing surveillance and ongoing research.

Regulatory Agency Approvals

Aimovig
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia
  • Swissmedic (CH)
  • Medsafe (NZ)
Ubrelvy
  • Food and Drug Administration (FDA), USA

Access Aimovig or Ubrelvy today

If Aimovig or Ubrelvy are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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