RecruitingPhase 2NCT06699121
A Study to Assess the Safety and Efficacy of LB-P8 in Patients With PSC
Studying Primary sclerosing cholangitis
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
- LISCure Biosciences
- Intervention
- LB-P8 low-dose(drug)
- Enrollment
- 87 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2025 – 2029
Study locations (7)
- University of California Davis, Sacramento, California, United States
- UCHealth University of Colorado Hospital, Aurora, Colorado, United States
- University Of Iowa Hospitals And Clinics, Iowa City, Iowa, United States
- Mercy Medical Center, Baltimore, Maryland, United States
- Mayo Clinic, Rochester, Minnesota, United States
- The Vanderbilt Clinic, Nashville, Tennessee, United States
- Liver institute Northwest, Seattle, Washington, United States
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.
Open NCT06699121 on ClinicalTrials.govOther trials for Primary sclerosing cholangitis
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