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RECRUITING
NCT06603558

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

Sponsor: AbbVie

View on ClinicalTrials.gov

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.

Official title: Post-marketing Surveillance Study to Evaluate the Safety and Effectiveness of Atogepant for the Prevention of Migraine in Korean Adult Patients

Key Details

Gender

All

Age Range

19 Years - Any

Study Type

OBSERVATIONAL

Enrollment

3000

Start Date

2024-09-24

Completion Date

2029-05

Last Updated

2026-01-20

Healthy Volunteers

No

Interventions

DRUG

Atogepant

Oral Tablet

Locations (4)

Hallym University Dongtan Sacred Heart Hospital /ID# 273581

Hwaseong, Gyeonggido, South Korea

Seoul National University Hospital /ID# 271892

Seoul, Seoul Teugbyeolsi, South Korea

Kangbuk Samsung Hospital /ID# 271893

Seoul, Seoul Teugbyeolsi, South Korea

Yonsei University Health System Severance Hospital /ID# 272639

Seoul, Seoul Teugbyeolsi, South Korea