What is Ubrelvy (ubrogepant)?

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Ubrelvy (Ubrogepant): An Oral CGRP Receptor Antagonist for Acute Migraine Treatment

Ubrelvy (ubrogepant) is an oral calcitonin gene-related peptide (CGRP) receptor antagonist FDA-approved for the acute treatment of migraine attacks with or without aura in adults. 1

Mechanism and Classification

  • Ubrogepant works by antagonizing CGRP receptors, which play a key role in migraine pathophysiology 1
  • It belongs to the "gepant" class of medications, specifically designed for migraine treatment 1
  • Unlike triptans, ubrogepant does not cause vasoconstriction, potentially making it suitable for patients with cardiovascular contraindications 2, 3

Clinical Indications and Efficacy

  • Ubrogepant is indicated only for acute treatment of migraine attacks and is not approved for preventive therapy 1
  • The 2023 VA/DoD Clinical Practice Guideline for Headache Management suggests ubrogepant for the short-term treatment of migraine (weak recommendation) 4
  • Clinical trials demonstrated that ubrogepant is effective for:
    • Pain freedom at 2 hours (21.8% for 50mg dose vs 14.3% for placebo) 2
    • Relief from most bothersome migraine-associated symptom at 2 hours (38.9% for 50mg dose vs 27.4% for placebo) 2
    • Reduction in photophobia and phonophobia 1

Dosing and Administration

  • Available in 50mg and 100mg oral tablets 1
  • Can be taken with or without food 1
  • Most patients can take a second tablet 2 hours after the first tablet if needed 1
  • Important limitation: It is not known if it's safe to take Ubrelvy for more than 8 migraine headaches in 30 days 1

Drug Interactions

  • Contraindicated with strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin, itraconazole) 1
  • Dose adjustments needed with moderate CYP3A4 inhibitors including:
    • Verapamil, cyclosporine, ciprofloxacin, fluconazole, fluvoxamine 1
    • Second dose should not be taken within 24 hours when using these medications or consuming grapefruit juice 1

Safety Profile and Adverse Effects

  • Most common adverse events (occurring in ≥2% of patients):
    • Nausea (2.0-2.5%)
    • Dizziness (1.4-2.1%)
    • Somnolence and dry mouth may also occur 3
  • Allergic reactions can occur, though most are not serious and occur within hours of taking the medication 1
  • Recent research shows that ubrogepant can be safely used concomitantly with atogepant (a CGRP antagonist for migraine prevention) 5

Emerging Applications

  • Recent research demonstrates efficacy when administered during the migraine prodrome phase:
    • Significantly prevents onset of moderate or severe headache 6
    • Improves ability to function normally over 24 hours 7
    • Reduces activity limitations and increases patient satisfaction 7

Comparison to Other Migraine Treatments

  • The VA/DoD guidelines strongly recommend triptans (eletriptan, frovatriptan, rizatriptan, sumatriptan, zolmitriptan) and aspirin-acetaminophen-caffeine combination as first-line acute treatments 4
  • Ubrogepant and rimegepant (another gepant) have weaker recommendations but may be appropriate alternatives for patients who cannot tolerate or have contraindications to first-line treatments 4

Important Clinical Considerations

  • Patients should track their headaches and medication use to monitor effectiveness and stay within the recommended monthly limit 1
  • Pregnancy registry exists for women who take Ubrelvy during pregnancy, as effects on unborn babies are unknown 1
  • Not known if Ubrelvy passes into breast milk 1

Remember to document headache characteristics before and after treatment to assess response and guide future management decisions.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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