A Case of Acute Migraine Without Aura Treated With a New FDA-Approved Medication Ubrogepant
Maria A Shamsi, Mohammad A Khalid

TL;DR
A new FDA-approved drug called ubrogepant significantly reduced migraine severity and disability in a patient who had not responded to other treatments.
Contribution
This case report demonstrates ubrogepant's efficacy in reducing migraine duration by more than 50%, a novel finding not previously documented.
Findings
Ubrogepant reduced headache duration from 36-60 hours to less than 12 hours.
The patient's headache severity decreased from 7.5/10 to 3/10 after treatment.
Migraine-related disability and quality of life improved significantly.
Abstract
Ubrogepant is the first medication that blocks calcitonin gene-related peptide (CGRP), a protein released during a migraine attack, from binding to its receptors. Ubrogepant has shown positive safety, efficacy, and tolerability results for the treatment of acute migraine in phase 3 randomized trials. At this time, there are very few case reports on ubrogepant. Herein, we describe a complex patient with treatment-resistant migraine who showed substantial improvement in migraine severity, duration, and overall disability after using ubrogepant. A 46-year-old woman with a 25-year history of migraine presented with an improvement in headache severity, duration, and disability after using a new FDA-approved medication, ubrogepant, for less than five months. Before commencing ubrogepant,her headache duration hours ranged from 36 to 60 hours, headache severity was rated 7.5/10, and mean…
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Taxonomy
TopicsMigraine and Headache Studies · Trigeminal Neuralgia and Treatments · Neurological Disorders and Treatments
