Clinical Drug Experience Knowledgebase

Criteria

Inclusion Criteria:

Healthy male subject of caucasian origin 18 to 45 years of age
Good state of health (mentally and physically) as determined by medical history, physical examination, vital signs, ECG recording and clinical lab results.
BMI in between 20-29 kg/m² with absolute weight in between 70-120 kg.
Serum triglyceride, total cholesterol and liver enzyme levels (alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyltransferase (GGT), alkaline phosphatase (AP)) strictly within the normal ranges at screening and on Day -1.
HbA1c ≤ 6.5 %
Subject has been informed both verbally and in writing and has given written consent to participation in the study prior to start and any study-related procedure
Negative results for HIV- and Hepatitis-B and -C serology at screening

Exclusion Criteria:

Female gender
Use of prescription or non-prescription drugs within 7 days (30 if the drug is a possible enzyme inducer) prior to administration of study medication. Use of drugs known to induce steatosis (e.g. valproate, amiodarone or prednisone) or to affect body weight and carbohydrate metabolism
Any acute or chronic illness or clinically relevant finding at screening and at base line examination which may jeopardize the subject's participation in the study
History or presence of biliary obstruction or biliary disease, hepatic encephalopathy, advanced ascites, portal hypertension, esophageal/gastric variceal bleeding, hepatocellular carcinoma, previous liver transplantation or any other chronic liver disease
Renal dysfunction, e.g. glomerular filtration rate ≤ 80 ml/min/1,73m2 (as determined by the formula of Cockroft-Gault)
Type I or II Diabetes
Any clinically relevant abnormality on screening medical assessment, laboratory examination, 12-lead ECG Any clinically relevant finding in the baseline telemetry
Marked baseline prolongation of QT/QTc interval (QTc interval > 440 ms) in the 12-lead ECG using the Fridericia method for QTc analysis
Heart rate < 50 bpm.
Allergies (except for mild forms of hay fever) or history of hypersensitivity reactions
Smoking (regular or irregular) > 5 cigarettes (or equivalent) per day.
Excessive alcohol drinking (more than approximately 20 g alcohol per day), unable to refrain from alcohol drinking from 48 h prior to dosing until the last pharmacokinetic blood sample has been withdrawn
Positive test for drugs or alcohol at screening or prior to the dosing session
History of alcoholism or drug/chemical/substance abuse within past 2 years
Investigator deems the subject unable or unwilling to comply fully with the study protocol
Has received clinical study medication within the last 30 days prior to this study
Donation or loss of 400 ml or more of blood within eight (8) weeks prior to dosing
Allergic to any of the active or inactive ingredients in the study medication
Any other reason which the Investigator considers unsuitable for the subject to participate
All subjects (including male subjects with partners of childbearing potential) who do not use a highly effective method of birth control (failure rate less than 1 % per year when used consistently and correctly), e.g. implants, injectables, combined oral contraceptives in combination with a barrier method, some intrauterine contraceptive devices or sexual abstinence
Any condition or previous disease leading to puritus or itching of the skin.