UnknownPhase 2NCT05467553
A Study to Compare P1101 Plus TAF With or Without UDCA in Patients With HBV and HDV Co-Infection
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
- National Taiwan University Hospital
- Principal Investigator
- Pei-Jer ChenNational Taiwan University Hospital
- Intervention
- Ursodeoxycholic acid(drug)
- Enrollment
- 30 target
- Eligibility
- 20-75 years · All sexes
- Timeline
- 2023 – 2025
Study locations (2)
- National Taiwan University Hospital, Taipei, Taiwan
- Taipei Medical University Hospital, Taipei, Taiwan
Collaborators
PharmaEssentia
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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