Ubrogepant treatmeNt in mIgraine Patients Utilizing mOnoclonal aNtibodies

Running, not enrolling · Phase 4

Conditions studied: Headache, Migraine

In brief

This is a prospective open-label randomized study assessing similar endpoints included in the pivotal trial for ubrogepant, which are pain freedom and freedom from the most bothersome symptom at two hours. Patients between 18-75 years old with a one-year history of migraine who experience ≥3 migraine days/month will be screened. This study will include migraine patients treated with or without injectable CGRPmAbs. As was the case in the clinical trials, this will be a single-attack study. Patients will be randomized to treat a single migraine attack with ubrogepant 50mg or 100mg. Patients will record dosing time, most bothersome symptom (nausea, photophobia, or phonophobia - chosen by patient), pain freedom, pain relief, the use of a 2nd dose if required, and adverse reactions. Patients will follow up within 30 days post treatment. Patients will be assessed for adverse events, and the safety data will be compared with the original clinical trial.

Key facts

Study ID

NCT05503082

Run by

Chicago Headache Center & Research Institute

People needed

164

Starts

2022-09-06

Expected to finish

2024-11-01

Last updated by the study team

2024-08-20

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female patients ages 18 to 75 years, at screening (Visit 1).
• At least a 1-year history of migraine with or without aura.
• History of ≥3 monthly headache days of at least moderate severity.
• Study patient currently on CGRPmAbs must be on treatment > 1 month at screening.
• By history, the patient's migraines typically last between 4 and 72 hours if untreated or treated unsuccessfully and migraine episodes are separated by at least 48 hours of headache pain freedom

You may not qualify if…

• History of <3 monthly headache days of at least moderate severity
• Concomitant use of strong CYP3A4 inducers (e.g., phenytoin, barbiturates, rifampin, St. John's Wort)
• Concomitant use of strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole, clarithromycin)
• Currently on Botox treatment for CM.
• Concomitant use of gepants as a preventative treatment.
• Current user of illicit drugs, or a history within 1 year prior to screening (visit 1) of drug or alcohol abuse or dependence
• Clinically significant hematologic, endocrine, cardiovascular, pulmonary, gastrointestinal, or neurologic disease. If there is a history of such a disease, but the condition has been stable for more than 1 year prior to screening (visit 1) and is judged by the PI as not likely to interfere with participation in the study, the participant may be included.
• Woman is pregnant, planning to become pregnant during the course of the study, or currently lactating.

Where it is running

• Chicago Headache Center & Research Institute — Chicago, Illinois, United States
• Chicago Headache Center & Research Institute — Naperville, Illinois, United States

Full record on ClinicalTrials.gov

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