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A Study to Assess the Safety, Pharmacokinetics, and Efficacy of ABI-6250 in Participants With Chronic Hepatitis D Virus Infection
Sponsor: Assembly Biosciences
Summary
This study is designed to assess safety, pharmacokinetics, and efficacy ABI-6250 in participants with Chronic Hepatitis D Virus Infection.
Official title: A Phase 2, Multicenter, Open Label, Parallel-Group Study of the Safety, Pharmacokinetics, and Efficacy of ABI-6250 in Participants With Chronic Hepatitis D Virus Infection
Key Details
Gender
All
Age Range
18 Years - 70 Years
Study Type
INTERVENTIONAL
Enrollment
80
Start Date
2026-10
Completion Date
2028-09
Last Updated
2026-08-13
Healthy Volunteers
No
Conditions
Interventions
ABI-6250
Once daily tablet dosing for 48 weeks starting at Day 1 visit
ABI-6250
Once daily tablet dosing for 48 weeks, starting at Week 16 visit
Locations (22)
AP-HP - Beaujon Hospital
Clichy, France
Hôpital Henri-Mondor
Créteil, France
CHU Lyon - Hôpital Croix-Rousse
Lyon, France
LLC Neolab
Tbilisi, Georgia
Universitätsklinikum Hamburg-Eppendorf
Hamburg, Germany
Medizinische Hochschule Hannover
Hanover, Germany
Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico
Milan, Italy
Azienda Ospedaliera Universitaria
Naples, Italy
Clinical Republican Hospital
Chisinau, Moldova
New Zealand Clinical Research
Auckland, New Zealand
Aga Khan University Hospital
Karachi, Pakistan
Dr. Ziauddin Hospital
Karachi, Pakistan
Arensia Research Clinic
Bucharest, Romania
Dr. Victor Babes Foundation
Bucharest, Romania
Fundeni Clinical Institute
Bucharest, Romania
Prof. Dr. Matei Bals National Institute of Infectious Diseases
Bucharest, Romania
Hospital Clínico Universitario Lozano Blesa
Zaragoza, Spain
ARENSIA Exploratory Medicine Ivano-Frankivsk
Ivano-Frankivsk, Ukraine
Medical Center of LLC ARENSIA Exploratory Medicine
Kyiv, Ukraine
King's College Hospital London
London, United Kingdom
The Royal London Hospital
London, United Kingdom
North Manchester General Hospital
Manchester, United Kingdom