Observational Study of Oral Atogepant to Evaluate Real-World Effectiveness in Adult Participants With Migraine

Prior treatment

• Previously exposed to atogepant as routine therapy or from clinical trials experience prior to entry.

Other illness

• 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.

Other

• 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.

• 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.