Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
AbbVie
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
At least 1-year history of migraine with or without aura consistent with a diagnosis according to the International Classification of Headache Disorders (ICHD)-3, 2018.
Prescribed atogepant according to the relevant approved local label.
For participants who initiate atogepant at the prescribing physician or treating health care provider (HCP) discretion as part of their routine clinical care, the decision to administer atogepant must be made prior to and independent of recruitment into the study.
Willing and able to comply with the requirements of the study.
Not on concomitant preventive medication for migraine or have been on a stable preventive medication for migraine for at least 3 months prior to enrollment in the study. If on a stable preventive medication, the prescribing physician or treating HCP and participant must confirm that there is no plan to change concomitant preventive medication during the first 12 weeks of the study.
You may not be if
Previously exposed to atogepant as routine therapy or from clinical trials experience prior to entry.
Contraindications to atogepant as per local labeling.
Pregnant or planning to be pregnant or women of childbearing potential not using contraception.
Enrolled in any interventional studies that may include investigational compounds for migraine, or non-AbbVie observational studies.
In the opinion of the prescribing physician or treating HCP, the participant has a history or current evidence of any condition that might interfere with patient's ability to comply with the study requirements.
