search
Back to results

KRN7000 in Chronic Hepatitis B

Primary Purpose

Hepatitis B, Chronic

Status
Completed
Phase
Phase 1
Locations
Netherlands
Study Type
Interventional
Intervention
KRN7000
Sponsored by
Foundation for Liver Research
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatitis B, Chronic focused on measuring chronic, hepatitis b

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Chronic hepatitis B (confirmed by a liver biopsy performed within 3 years prior to the screenings visit and HBV DNA in serum >10E5 copies/ml at the screenings visit). ALT > 1.2 x ULN on two occasions documented within 8 weeks before initiation of treatment. Able and likely to attend regularly for treatment and follow-up. Written informed consent. Adequate contraception for males and females during treatment and follow-up (written confirmation). Exclusion Criteria: Patients with evidence of cirrhosis. Decompensated liver disease, as marked by: bilirubin greater than 20 micromol/L or serum albumin <35 g/L or prothrombin time greater than 3 seconds prolonged or Quick test below 70% or history of bleeding esophageal varices, ascites or hepatic encephalopathy. Systemic IFN treatment, systemic antiviral agents, systemic corticosteroids, immune suppressive treatment or any investigational drug within 3 months of entry to this protocol. Patients with ALT levels greater than 10 times ULN will not be enrolled but may be followed until three consecutive determinations within 2 months are below this level. Pregnancy, or in women of child-bearing potential or in spouses of such women, inability to practice adequate contraception. Significant systemic or major illnesses other than liver disease, including congestive heart failure, ischemic heart disease, angina pectoris, cerebrovascular disease, renal failure (creatinine clearance less than 50 ml/min), organ transplantation, serious psychiatric disease or depression, anaphylactic disorder. Pre-existing severe cytopenia; Hb<7 mmol/L, WBC <3x10E9/L, Plt <100x10E9/L, Lymphocyte <0.5x10E9/L. Any history or presence of autoimmune disease. Evidence of hepatocellular carcinoma; alpha-fetoprotein (AFP) levels greater than 50 ng/ml and ultrasound (or other imaging study) within 6 months prior to the entry demonstrating a mass suggestive of liver cancer. Human immunodeficiency virus infection, as shown by presence of anti-HIV antibody. Patients with cerebroside metabolite abnormalities (e.g. Gaucher's disease). Other acquired or inherited causes of liver disease: hepatitis C, hepatitis D, alcoholic liver disease, obesity induced liver disease, drug related liver disease, auto-immune liver disease, Wilson's disease, hemochromatosis, alpha-1-antitrypsin deficiency. Any other condition which in the opinion of the investigator would make the patient unsuitable for enrollment, or could interfere with the patient participating in and completing the study.

Sites / Locations

  • Erasmus MC, University Medical Center Rotterdam

Outcomes

Primary Outcome Measures

To determine safety and tolerability

Secondary Outcome Measures

To evaluate effectiveness in reducing HBV DNA load
To evaluate effectiveness in inducing immunological responses
TO evaluate effectiveness in normalization of ALT

Full Information

First Posted
August 10, 2006
Last Updated
August 10, 2006
Sponsor
Foundation for Liver Research
search

1. Study Identification

Unique Protocol Identification Number
NCT00363155
Brief Title
KRN7000 in Chronic Hepatitis B
Official Title
Phase I/II Trial of KRN7000 in Patients With Chronic Hepatitis B Infection
Study Type
Interventional

2. Study Status

Record Verification Date
August 2006
Overall Recruitment Status
Completed
Study Start Date
March 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Foundation for Liver Research

4. Oversight

5. Study Description

Brief Summary
The purpose of this trial is to determine the safety, tolerability and effectiveness of KRN7000 for chronic hepatitis B infection.
Detailed Description
KRN7000 is reported to inhibit HBV replication in HBV transgenic mice. Anti-viral effects of KRN7000 can be expected in HBV, as the compound is able to induce not only IFN-alpha/beta but also IFN-gamma and TNF-alpha. In two clinical trials, KRN7000 was safe in both healthy volunteers and solid cancer patients; particularly, the compound has not been reported to show drug-related serious adverse events. A phase I/II trial is of significance in assessing the safety and efficacy of KRN7000 treatment for CHB patients. The 300 microgram/m2 dose level, comparable to 10 microgram/kg, can be considered as the highest safe dose level for the phase I/II trial for CHB patients with 3 dose levels. Dose incrementation will be performed in a logarithmic manner: 0.1, 1 and 10 microgram/kg. In the phase I trial for solid tumor patients, weekly administration of KRN7000 did not allow sufficient time for NKT cell recovery. As KRN7000 is reported to be an activating ligand for NKT cells, it is logical to assume that a dosing interval that provides time for recovery of NKT cells is optimal. In fact, cytokine production after repeating dosing, when NKT cells were hardly detected in the peripheral blood, was not observed. As it took approximately 4 weeks for NKT cells to recover to pre-dose levels after a single administration, monthly administration is now proposed for this trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B, Chronic
Keywords
chronic, hepatitis b

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
28 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
KRN7000
Primary Outcome Measure Information:
Title
To determine safety and tolerability
Secondary Outcome Measure Information:
Title
To evaluate effectiveness in reducing HBV DNA load
Title
To evaluate effectiveness in inducing immunological responses
Title
TO evaluate effectiveness in normalization of ALT

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chronic hepatitis B (confirmed by a liver biopsy performed within 3 years prior to the screenings visit and HBV DNA in serum >10E5 copies/ml at the screenings visit). ALT > 1.2 x ULN on two occasions documented within 8 weeks before initiation of treatment. Able and likely to attend regularly for treatment and follow-up. Written informed consent. Adequate contraception for males and females during treatment and follow-up (written confirmation). Exclusion Criteria: Patients with evidence of cirrhosis. Decompensated liver disease, as marked by: bilirubin greater than 20 micromol/L or serum albumin <35 g/L or prothrombin time greater than 3 seconds prolonged or Quick test below 70% or history of bleeding esophageal varices, ascites or hepatic encephalopathy. Systemic IFN treatment, systemic antiviral agents, systemic corticosteroids, immune suppressive treatment or any investigational drug within 3 months of entry to this protocol. Patients with ALT levels greater than 10 times ULN will not be enrolled but may be followed until three consecutive determinations within 2 months are below this level. Pregnancy, or in women of child-bearing potential or in spouses of such women, inability to practice adequate contraception. Significant systemic or major illnesses other than liver disease, including congestive heart failure, ischemic heart disease, angina pectoris, cerebrovascular disease, renal failure (creatinine clearance less than 50 ml/min), organ transplantation, serious psychiatric disease or depression, anaphylactic disorder. Pre-existing severe cytopenia; Hb<7 mmol/L, WBC <3x10E9/L, Plt <100x10E9/L, Lymphocyte <0.5x10E9/L. Any history or presence of autoimmune disease. Evidence of hepatocellular carcinoma; alpha-fetoprotein (AFP) levels greater than 50 ng/ml and ultrasound (or other imaging study) within 6 months prior to the entry demonstrating a mass suggestive of liver cancer. Human immunodeficiency virus infection, as shown by presence of anti-HIV antibody. Patients with cerebroside metabolite abnormalities (e.g. Gaucher's disease). Other acquired or inherited causes of liver disease: hepatitis C, hepatitis D, alcoholic liver disease, obesity induced liver disease, drug related liver disease, auto-immune liver disease, Wilson's disease, hemochromatosis, alpha-1-antitrypsin deficiency. Any other condition which in the opinion of the investigator would make the patient unsuitable for enrollment, or could interfere with the patient participating in and completing the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Harry LA Janssen, MD, PhD
Organizational Affiliation
Dept. of Gastroenterology & Hepatology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands
Official's Role
Principal Investigator
Facility Information:
Facility Name
Erasmus MC, University Medical Center Rotterdam
City
Rotterdam
ZIP/Postal Code
3015GD
Country
Netherlands

12. IPD Sharing Statement

Learn more about this trial

KRN7000 in Chronic Hepatitis B

We'll reach out to this number within 24 hrs