Last updated: 11/04/2018 04:31:48
Adefovir Dipivoxil For The Treatment Of Patients With Chronic Hepatitis B Related Advanced Fibrosis Or Cirrhosis
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Completed
Completed
Trial overview
Official title: An open label study of adefovir dipivoxil for the treatment of patients with chronic hepatitis B related advanced fibrosis or cirrhosis.
Trial description: This 36-month open-label study of adefovir dipivoxil investigates the clinical benefits of the therapy in chronic hepatitis B patients with advanced fibrosis or cirrhosis confirmed with biopsy. Primary endpoint is histological improvement defined as a decrease of Ishak Fibrosis Score by one point or more from baseline at Month 36 of adefovir dipivoxil treatment. Approximately 150 patients will be recruited in study centres in the Asia Pacific area. The patients are offered 36 months of open label adefovir dipivoxil treatment, with assessments every three months, after which there is a 6-month post study treatment follow-up prior to study completion. After the 36 months of study treatment, it is likely that the patient will benefit from continued treatment with adefovir dipivoxil. If this is the case in the investigators clinical judgement, the investigator should ensure that a routine prescription is available in a timely manner, and that no unnecessary interruption in treatment occurs.
Primary purpose:
Treatment
Trial design:
Single Group Assignment
Masking:
None (Open Label)
Allocation:
Non-randomized
Primary outcomes:
Number of participants with histologic improvement at Month 36 (Intent-to-Treat Population)
Timeframe: Screening and Month 36
Number of participants with histologic improvement at Month 36 (Per Protocol Population)
Timeframe: Screening and Month 36
Secondary outcomes:
Number of participants with a reduction from baseline in the Child-Pugh score by 2 points or more at Months 12, 24, and 36
Timeframe: Baseline and Months 12, 24, and 36
Number of participants with a reduction from Screening of at least 2 points in the Knodell necroinflammation score at Month 36
Timeframe: Screening and Month 36
Change from baseline in serum hepatitis B virus (HBV) deoxyribonucleic acid (DNA) level at Months 12, 24, and 36
Timeframe: Baseline and Months 12, 24, and 36
Number of participants achieving virological response (HBV DNA level <= 10^3 copies/ml) at Months 12, 24, and 36
Timeframe: Months 12, 24, and 36
Number of participants achieving virological response (HBV DNA level <= 10^4 copies/ml) at Months 12, 24, and 36
Timeframe: Months 12, 24, and 36
Number of participants with undetectable HBV DNA at Months 12, 24, and 36
Timeframe: Months 12, 24, and 36
Number of participants with virological breakthrough at Months 12, 24, and 36
Timeframe: Months 12, 24, and 36
Number of participants with alanine aminotransferase (ALT) normalization at Months 12, 24, and 36
Timeframe: Months 12, 24, and 36
Number of participants who were Hepatitis B envelope antigen (HBeAg) positive at baseline and developed undetectable levels of HBeAg at Months 12, 24, and 36
Timeframe: Baseline and Months 12, 24, and 36
Number of participants who were HBeAg positive at baseline, with HBeAg seroconversion at Months 12, 24, and 36
Timeframe: Baseline and Months 12, 24, and 36
Number of participants who were Hepatitis B surface antigen (HBsAg) positive at baseline and developed undetectable levels of HBsAg at Months 12, 24, and 36
Timeframe: Baseline and Months 12, 24, and 36
Number of participants who were HBsAg positive at baseline, with HBsAg seroconversion at Months 12, 24, and 36
Timeframe: Baseline and Months 12, 24, and 36
Interventions:
Drug: adefovir dipivoxil
Enrollment:
155
Observational study model:
Not applicable
Primary completion date:
2009-24-09
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Hepatitis B, Chronic, Cirrhosis, Fibrosis
Product
adefovir
Collaborators
Not applicable
Study date(s)
May 2005 to September 2009
Type
Interventional
Phase
4
Participation criteria
Sex
Female & Male
Age
18+ years
Accepts healthy volunteers
No
- Male or female patients ≥ 18 years of age
- A female is eligible to enter and participate in this study if she is of: a) non-childbearing potential (ie. Physiologically incapable of becoming pregnant, including any female who is pre-menarchal or post-menopausal); b) child-bearing potential with a negative serum pregnancy test at screen, and agrees to one of the following: -complete abstinence from intercourse from 2 weeks prior to administration of the study drug, throughout the study, and for a time interval after completion or premature discontinuation from the study to account for elimination of the investigational drug, (a minimum of 5 half-lives or longer if the pharmacodynamic profile of the investigational drug warrants a longer time period); or, -Female sterilization; or -Sterilization of male partner; or -Implants of levonorgestrel; or, -Injectable progestogen; or -Oral contraceptive (combined or progestogen only); or, -Any intrauterine device (IUD) with published data showing that the lowest expected failure rate is less that 1% per year (not all IUDs meet this criterion); or, -Any other methods with published data showing that the lowest expected failure rate for that method is less than 1% per year; or, -Barrier method only if used in combination with any of the above acceptable methods.
- 1. ALT >10XULN at screening
- 2. Child-Pugh Score ≥ 7
Inclusion and exclusion criteria
Inclusion criteria:
- Male or female patients ≥ 18 years of age
- A female is eligible to enter and participate in this study if she is of: a) non-childbearing potential (ie. Physiologically incapable of becoming pregnant, including any female who is pre-menarchal or post-menopausal); b) child-bearing potential with a negative serum pregnancy test at screen, and agrees to one of the following: -complete abstinence from intercourse from 2 weeks prior to administration of the study drug, throughout the study, and for a time interval after completion or premature discontinuation from the study to account for elimination of the investigational drug, (a minimum of 5 half-lives or longer if the pharmacodynamic profile of the investigational drug warrants a longer time period); or, -Female sterilization; or -Sterilization of male partner; or -Implants of levonorgestrel; or, -Injectable progestogen; or -Oral contraceptive (combined or progestogen only); or, -Any intrauterine device (IUD) with published data showing that the lowest expected failure rate is less that 1% per year (not all IUDs meet this criterion); or, -Any other methods with published data showing that the lowest expected failure rate for that method is less than 1% per year; or, -Barrier method only if used in combination with any of the above acceptable methods.
- Documented chronic hepatitis B infection determined by presence of serum HBsAg for at least 6 months (positive once at least 6 months before screening and at time of screening visit.)
- Positive HBV DNA plasma assay with screening value ≥ 1 x 10^5 copies /mL. (Roche COBAS AMPLICOR TM HBV Monitor Test, LLOD <300 copies/mL )
- Adequate renal function defined as serum creatinine ≤1.5 mg/dL (≤130 µmol/L).
- Willing and able to undergo two liver biopsies (prior to dosing, and after 36 months of therapy). The study baseline liver biopsy can be the most recent liver biopsy taken within 6 months of enrollment, as long as the biopsy was taken 6 months or more after the completion of any interferon or 3 months or more after completion of any antiviral treatment (eg. famciclovir, lamivudine etc.), and the patient has not had interferon therapy or any antiviral therapy between the biopsy and screening.
- Liver biopsy showing advance fibrosis/cirrhosis (Ishak fibrosis score ≥4). The slides must be available for review by an independent histopathologist.
- Availability and willingness of the subject to provide written informed consent per ICH/GCP and local Guidelines.
Exclusion criteria:
- 1. ALT >10XULN at screening 2. Child-Pugh Score ≥ 7 3. History of acute exacerbation leading to transient decompensation 4. Co-infections with HIV, HCV or HDV. Note: Patients who are anti-HCV seropositive and in whom HCV RNA is undetectable are considered to be HCV seropositive and will not be eligible for enrollment. 5. Any of the following laboratory parameter within 4 weeks prior to study entry: -Haemoglobin <8.0 g/dL, -Absolute neutrophil count (ANC) < 1.5 x 10^9/L, -Platelet count ≤50 x 10^9/L, -Pancreatic amylase and/or lipase >2 x ULN
- Screening alpha-fetoprotein (AFP) value >50 ng/mL
- Clinical, ultrasonographic or radiologic evidence of hepatic mass suggestive of hepatocellular carcinoma.
- Significant concurrent medical and/or psychiatric conditions other than hepatitis B that in the opinion of the investigators might interfere with patient's treatment, assessment or compliance according to study requirement, such as malignancy, congestive heart failure, renal failure, chronic pancreatitis, diabetes mellitus with poor control and alcoholism.
- Any of the following medications with 2 months prior to study entry (or the expectation that subject will receive these during the course of the study): -Nephrotoxic medication (eg aminoglycosides, amphotericin B, vancomycin, cidofovir, foscarnet, cisplatin, pentamidine) or competitors or renal excretion (eg probenecid, sulfinpyrazone), -Hepatotoxic medication (eg anabolic steroids,ketoconazole, itraconazole, isoniazid, rifampin, rifabutin).
- Treatment with immunosuppressive/immunomodulatory agents (including interferon and corticosteroids) within 6 months prior to study entry.
- Presence of other causes of liver disease (ie. hemochromatosis, Wilson's disease, alcoholic liver disease, non-alcoholic steatohepatitis, autoimmune hepatitis, alpha-1 antitrypsin deficiency).
- A history of liver transplantation /planned for liver transplantation.
- Pregnancy (or lactation) or , in subjects capable of bearing children, inability/unwillingness to practice adequate contraception.
- Females of child-bearing potential (post-puberty) willing or unable to have pregnancy testing at any study visit.
- History of hypersensitivity to nucleoside and/or nucleotide analogues.
- Concurrent participation in another clinical trial in which the subject is or will be exposed to another investigational or a non-investigational drug or device within 30 days of the screening visit.
Trial location(s)
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Completed
Actual primary completion date
2009-24-09
Actual study completion date
2009-24-09
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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