CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 22 enrolled
Drug / intervention
Lonafarnib +2 moredrug
Likely dose
Lonafarnib 50 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02511431
NCT02511431Phase 2Completed

Treatment of Chronic Delta Hepatitis With Lonafarnib and Ritonavir

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)·interventional·Posted Jul 30, 2015·Updated Sep 25, 2018

In Brief

A Phase 2 clinical trial evaluating Lonafarnib, Ritonavir, and 1 other intervention for Hepatitis D. Completed, enrolled 22 participants across 1 site.

Detailed Summary

Background: \- Chronic hepatitis D is a liver disease caused by the hepatitis D virus (HDV). It can be severe and progressive. Most people with hepatitis D will develop scarring and damage to the liver. There is no FDA approved drug to treat chronic hepatitis D. Researchers want to know if the drugs lonafarnib and ritonavir can help people with chronic hepatitis D. Objective: \- To find out if treatment of hepatitis D with lonafarnib and ritonavir is safe and effective. Eligibility: \- People 18 years of age and older with chronic hepatitis D. They must not have HIV or other major illnesses. Design: * Participants will be screened with medical history, physical exams, and blood tests. * Participants will have 24 weeks of treatment. They will then have 24 weeks of follow-up. * Participants will be in 1 of 6 treatment groups. Those in each group will receive different doses of the study drugs. Some groups will start with placebo but will receive treatment after 3 months of placebo. * Participants will also take drugs to treat hepatitis B. * Participants will have many visits. These will include: * One three-day stay at the Clinical Center * Physical exams * EKG: small sticky patches will be put on the chest, arms, and legs to trace heart rhythm * Ultrasounds of the abdomen * Urine and blood tests * Stool samples * Eye exams * Evaluations by a reproductive endocrinologist (women) or urologist (men). Men may provide a sperm sample (optional).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHepatitis D
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedJul 30, 2015
Enrollment StartJul 29, 2015
Primary CompletionFeb 23, 2017
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 10.9 years ago

Interventions

Lonafarnibdrug

prenylation inhibitor to be administered daily at doses of 50 mg, 75 mg or 100 mg.

Ritonavirdrug

FDA approved drug for use of boosting other drugs. Will be used to boost Lonafarnib as they both use the same cytochrome P450 system. Will be administered at 100 mg daily.

Placeboother

Placebo