RecruitingNot applicableNCT07479056
Fexuprazan for Prevention of Upper Gastrointestinal Bleeding in High Bleeding Risk Patients Receiving Dual Antiplatelet Therapy
Studying Acrocallosal syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- SUK MIN SEO
- Principal Investigator
- Suk Seo, MD, PhDThe Catholic University of Korea Eunpyeong St. Mary's Hospital
- Intervention
- Fexuprazan 40mg(drug)
- Enrollment
- 400 target
- Eligibility
- 20 years · All sexes
- Timeline
- 2024 – 2028
Study locations (1)
- The Catholic University of Korea, Eunpyeong St. Mary's Hospital, Seoul, Eunpyeong-gu, South Korea
Collaborators
Daewoong Pharmaceutical Co. LTD.
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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