RecruitingPHASE1, PHASE2NCT07096193
Study of GS-4321 in Healthy Participants and Participants With Chronic Hepatitis Delta Virus
Studying Hepatitis delta
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
- Gilead Sciences
- Principal Investigator
- Gilead Study DirectorGilead Sciences
- Intervention
- GS-4321(drug)
- Enrollment
- 107 target
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2025 – 2029
Study locations (8)
- Investigative Site, Anaheim, California, United States
- IMSP Spitalul Clinic de Boli Infectioase "Toma Ciorba", Chinsinau, Moldova
- PMSI Clinical Republican Hospital "Timofei Mosneaga", Chisinau, Moldova
- Korea University Ansan Hospital, Ansan-si, South Korea
- The Catholic University of Korea Bucheon St. Mary's Hospital, Bucheon-si, South Korea
- The Catholic University of Korea, Seoul St. Mary's Hospital, Seoul, South Korea
- Samsung Medical Center, Seoul, South Korea
- Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung City, Taiwan
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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