CompletedPhase 2NCT03546621

A Multicenter, Open-label, Randomized Clinical Study to Assess Efficacy and Safety of 3 Doses of Myrcludex B for 24 Weeks in Combination With Tenofovir Compared to Tenofovir Alone to Suppress HBV Replication in Patients With Chronic Hepatitis D

Studying Hepatitis delta

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Key facts

Sponsor
Hepatera Ltd.
Principal Investigator
Heiner Wedemeyer, MD,PhD
Dept. of Gastroenterology, Hepatology and Endocrinology Medizinische Hochschule Hannover
Intervention
Myrcludex B(drug)
Enrollment
120 target
Eligibility
18-65 years · All sexes
Timeline
20162018

Study locations (15)

Collaborators

Data Matrix Solutions

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 NCT03546621 on ClinicalTrials.gov

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