Post-Marketing Study to Assess the Safety and Effectiveness of Oral Atogepant in Korean Adult Participants for the Prevention of Chronic or Episodic Migraine

Study Identifier
P24-480
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Study Details

Medical Condition
  • Migraine - Chronic
  • Migraine - Episodic
  • Migraine - General
  • Study Drug
  • Atogepant
  • Phase
    N/A
    Sex
    Female & Male
    Age
    19+ years

    Protocol Summary

    Migraine is a neurological disease characterized by moderate or severe headache, associated with nausea, vomiting, and/or sensitivity to light and sound. The study will assess the safety and effectiveness of atogepant for the preventive treatment of migraine in Korean adult patients with chronic migraine or episodic migraine under routine clinical practice.

    Atogepant is an approved drug for preventive treatment of migraine in adults. Approximately 3000 adult participants who are prescribed atogepant by their doctors will be enrolled in this study in Korea.

    Participants will receive atogepant oral tablets as prescribed by their physician. Participants will be followed for up to week 12.

    There is expected to be no additional burden for participants in this trial. Participants will attend regular visits during the study at a hospital or clinic according to their routine clinical practice.

    Study Locations

    Location
    Status
    Location
    Hallym University Dongtan Sacred Heart Hospital /ID# 273581
    Hwaseong, Gyeonggido, Republic of Korea, 18450
    Status
    Recruiting
    Location
    Seoul National University Hospital /ID# 271892
    Seoul, Seoul Teugbyeolsi, Republic of Korea, 03080
    Status
    Recruiting
    Location
    Kangbuk Samsung Hospital /ID# 271893
    Seoul, Seoul Teugbyeolsi, Republic of Korea, 03181
    Status
    Recruiting
    Location
    Yonsei University Health System Severance Hospital /ID# 272639
    Seoul, Seoul Teugbyeolsi, Republic of Korea, 03722
    Status
    Recruiting