Status:
COMPLETED
Effects of Exenatide (Byetta®) on Liver Function in Patients With Nonalcoholic Steatohepatitis (NASH)
Lead Sponsor:
Ruhr University of Bochum
Conditions:
Nonalcoholic Fatty Liver Disease
Eligibility:
All Genders
18-75 years
Phase:
PHASE4
Brief Summary
The primary objective is to test the hypothesis that 24 weeks of treatment with exenatide will improve the histological acitvity of NASH (steatosis,necroinflammation, ballooning), summarized in the re...
Detailed Description
Non alcoholic steatohepatitis (NASH), a chronic liver disease characterized by insulin resistance, accumulation of hepatic fat and hepatocellular necroinflammation, has been recognized as a leading ca...
Eligibility Criteria
Inclusion
- Age between 18 and 75 years, inclusive.
- Patients present with histologically proven non-alcoholic steatohepatitis ascertained by the single center pathologist between visit 1 and 2
- First liver biopsy was obtained not later than 6 months before visit 1
- Patients have HbA1c not exceeding 10.0%.
- Patients have a history of stable body weight (not varying by \>10% for at least 3 months prior to screening
Exclusion
- Patients are investigator site personnel directly affiliated with the study, or are immediate family of investigator site personnel directly affiliated with the study. Immediate family is defined as a spouse, parent, child, or sibling, whether biological or legally adopted.
- Females of childbearing potential who are pregnant, breast-feeding or intend to become pregnant or are not using adequate contraceptive methods (adequate contraceptive measures include sterilisation, hormonal intrauterine devices, oral contraceptives, sexual abstinence or vasectomised partner). A male subject who is sexually active and has not been surgically sterilised must be informed that he must either use a condom during intercourse, ensure that his partner practices contraception, or he must refrain from sexual intercourse during the trial and until 1 month after completion of the trial. This is to prevent the possibility of a pregnancy from spermatocytes that can potentially be damaged by trial medication. It is strongly recommended that the female partners use a highly effective contraception (Pearl Index \< 1%).
- Patients have participated in an interventional medical, surgical, or pharmaceutical study (a study in which an experimental, drug, medical, or surgical treatment was given) within 30 days prior to screening. This criterion includes drugs that have not received regulatory approval for any indication at the time of study entry.
- Patients with evidence of viral or autoimmune hepatitis (positive testing for HBsAG, anti-HCV or anti-HIV, pos. AMA-screen, ANA-titer \> 1:160)
- Patients with inherited liver diseases (e.g. Wilson's disease, Hemochromatosis)
- Patients have alcohol consumption (\>20 g daily for males and \>10 g daily for females)
- Patients have decompensated liver cirrhosis (Child-Pugh score \>7)
- Patients have alanine aminotransaminase (ALT) greater than ten times the upper limit of the reference range.
- Patients have had greater than three episodes of severe hypoglycemia within 6 months prior to screening.
- Patients are undergoing therapy for a malignancy, other than basal cell or squamous cell skin cancer.
- Patients have cardiac disease that is Class III or IV, according to the New York Heart Association criteria.
- Patients have a known allergy or hypersensitivity to exenatide, or excipients contained in these agents.
- Patients have or had concomitant medication with thiazolidinediones.
- Patients have a history of renal transplantation or are currently receiving renal dialysis or have serum creatinine \>1.8 mg/dL for males and greater than or equal to \>1.5 mg/dL for females.
- Patients have known hemoglobinopathy or chronic anemia
- Patients are receiving chronic (lasting longer than 2 weeks) systemic glucocorticoid therapy (excluding topical and inhaled preparations) or have received such therapy within 2 weeks immediately prior to screening.
- Patients have used any prescription drug to promote weight loss within 3 months prior to screening.
- Patients have any other condition (including known drug or alcohol abuse or psychiatric disorder) that precludes them from following and completing the protocol, in the opinion of the investigator.
- Patients fail to satisfy the investigator of suitability to participate for any other reason.
Key Trial Info
Start Date :
July 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2010
Estimated Enrollment :
13 Patients enrolled
Trial Details
Trial ID
NCT01208649
Start Date
July 1 2008
End Date
September 1 2010
Last Update
September 24 2010
Active Locations (1)
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1
Department of Medicine I; University Hospital St. Josef-Hospital
Bochum, Germany, 44791