Status:
COMPLETED
Investigating the Pharmacokinetics, Safety and Tolerability After a Single Subcutaneous Injection of Semaglutide in Subjects With Mild, Moderate or Severe Hepatic Impairment Compared to Subjects With Normal Hepatic Function
Lead Sponsor:
Novo Nordisk A/S
Conditions:
Diabetes
Diabetes Mellitus, Type 2
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
This trial is conducted in Europe. The aim of this trial is to investigate the pharmacokinetics (the exposure of the trial drug in the body), safety and tolerability after a single injection of semagl...
Eligibility Criteria
Inclusion
- Male or female, age at least 18 years at the time of signing informed consent
- Body mass index (BMI) 18.5-40.0 kg/m\^2 (both inclusive)
- Only for subjects with hepatic impairment (mild, moderate and severe): A diagnosis of cirrhosis due to parenchymal liver disease, classified as Child-Pugh grade A,B or C as assessed by investigator and which is confirmed and documented by medical history, physical examination and at least one of the following: hepatic ultrasound,computerised axial tomography (CT) scan, magnetic resonance imaging (MRI), and/or liver biopsy
- Only for subjects with normal hepatic function: Subjects who are judged to be in good general health based on physical examination, medical history, ECG, vital signs, and the results of biochemistry, coagulation, haematology tests and urinalysis performed during the screening visit, as judged by the investigator
Exclusion
- Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential not using an adequate contraceptive method throughout the trial including the follow-up period (adequate contraceptive measures as required by local regulation or practice)
- Uncontrolled hypertension (defined as systolic blood pressure above or equal to 180 mmHg and/or diastolic blood pressure above or equal to 100 mmHg). If white-coat hypertension is suspected at the screening visit a repeated measurement at the screening visit is allowed
- Mental inability, unwillingness or language barrier precluding adequate understanding of or compliance with trial procedures
- Donation of any blood or plasma in the past month or in excess of 400 mL within the 3 months preceding screening, or surgery or trauma with more than 400 mL blood loss within the 3 months preceding screening
Key Trial Info
Start Date :
August 7 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 3 2015
Estimated Enrollment :
44 Patients enrolled
Trial Details
Trial ID
NCT02210871
Start Date
August 7 2014
End Date
June 3 2015
Last Update
December 21 2017
Active Locations (4)
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1
Novo Nordisk Investigational Site
Warsaw, Poland, 02-507
2
Novo Nordisk Investigational Site
Wołomin, Poland, 05-200
3
Novo Nordisk Investigational Site
Bratislava, Slovakia, 83101
4
Novo Nordisk Investigational Site
Bratislava, Slovakia, 833 05