Non-Alcoholic Fatty Liver Disease, Nonalcoholic Steatohepatitis
Conditions
Brief summary
This study is to evaluate the predictive value of NRL972 pharmacokinetics in the diagnosis of steatohepatitis using fatty liver disease as the comparator group. In addition, the sensitivity and specificity of NRL972 pharmacokinetics as a diagnostic tool will be compared to results from the standard laboratory tests, elastography, tests of metabolic markers and serum fibrosis markers frequently used in the evaluation of clinically predicted NAFLD patients. Patients will be included if they have clinical evidence of fatty liver disease and have been referred to the clinic for a diagnostic work-up, including a liver biopsy, blood tests and scans of the liver.
Detailed description
The study was conducted to describe and compare the plasma pharmacokinetics of NRL972 after a 15-second intravenous (i.v.) injection of 2 mg NRL972 against the diagnostic assessment based on liver biopsy in patients with clinically suspected NAFLD. A particular focus was to separate simple fatty liver disease (non-NASH) from non-alcoholic steatohepatitis (NASH) with or without cirrhosis (defined as advanced fibrosis: ≥F3) in a population likely to present with NAFLD. The study evaluated the predictive value of NRL972 pharmacokinetics in the diagnosis of NASH using fatty liver disease (non-NASH) as the comparator group in a population of clinically suspected NAFLD patients based on histological evaluation. The sensitivity and specificity of NRL972 pharmacokinetics as a diagnostic was compared to that of results from the standard laboratory tests, clinical features, elastography assessments for liver stiffness and tests of metabolic markers, serum fibrosis markers and established disease scores frequently used in the evaluation of NAFLD. The study also provided information on the safety and tolerability of i.v. doses of NRL972 under these conditions.
Interventions
DRUGNRL972
Single dose of 2 mg NRL972 administered intravenously. Total volume 5mL.
Sponsors
Norgine
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
Subjects meeting the following conditions will be eligible for enrollment: * Males or females (females of non-child-bearing potential or of child-bearing potential while taking medically appropriate contraception) * Any ethnicity * Age: 18 to 80 years of age * Clinical evidence of non-alcoholic liver disease requiring the conduct of a liver biopsy for the diagnosis of NAFLD and/or staging of disease severity * Willing and able to provide informed consent
Exclusion criteria
Subjects fulfilling any of the following criteria will be excluded from enrollment: General - all subjects * Presence of acute or chronic viral hepatitis confirmed by serology * Clinical signs of significant cholestasis * Liver impairment due to space-occupying processes (e.g. carcinoma) * Liver transplant recipient or patient scheduled for liver transplantation * Clinically evident rapidly deteriorating hepatic function * Significant bleeding diathesis * Esophageal bleeding within the 8 weeks prior to study entry * Presence of any contraindications for the conduct of the planned liver biopsy (e.g. allergy to lidocaine, coagulopathy with \<100 x109/L thrombocytes and/or INR \>1.3 * History of any allergic reaction to fluorescein * Presence of any acute infection * Previous participation in this trial * Having received any investigational drug or treatment within 30 days prior to study entry or requiring a concurrent treatment with any other experimental drug or treatment * Uncontrolled hypo- or hypertension (treated or untreated) with resting systolic blood pressure \>160 or \< 90 mmHg, diastolic blood pressure \>95 or \< 50 mmHg * Clinically relevant abnormal laboratory values indicating end-stage renal, pulmonary or cardiac disease * Known HIV infection * Concurrent alcohol use of more than 14 drinks (140g ethanol) for men and 7 drinks (70g ethanol) for women per week (each drink is counted as 10g ethanol) * History of drug or alcohol abuse within 2 months prior to dosing * Use of prohibited medication (section 4.8) * Donation of blood during the last 60 days or a history of blood loss exceeding 300 mL within the last 3 months * Suspicion or evidence that the subject is not trustworthy and reliable * Suspicion or evidence that the subject is not able to make a free consent or to understand the information in this regard * Significant side effects prior to the liver biopsy (e.g. anxiety requiring pre-medication) or after the biopsy (e.g. pain requiring i.v. pain medication, bleeding re-quiring medical intervention) General - all females * Positive pregnancy test * Pre-menopausal women not using appropriate contraception
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| C(30)/C(10) | 30 minutes post-dose | The primary efficacy variable was the NRL972 fractional retention ratio for 10 and 30 minutes post-dose (C30/C10) for different populations with NAFLD. |
| Adverse Events | Up to 2 hours post-dose | Primary safety assessment: Incidence of treatment-emergent adverse events |
| Vital Signs | Up to 2 hours post-dose | Primary safety assessment: continuous monitoring on automated cardiovascular systems |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| C(60) | 60 minutes post-dose | NRL972 fractional retention ratio for 60 minutes post-dose for different populations with NAFLD. |
| t1/2 | 60 minutes post-dose | apparent terminal disposition half-life |
| CL | 60 minutes post-dose | approximate overall clearance |
Countries
United States
Outcome results
None listed