- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02014259
Pharmacokinetics, Safety and Tolerability of Oral Semaglutide in Subjects With Various Degrees of Impaired Renal Function
April 17, 2018 updated by: Novo Nordisk A/S
Investigation of Pharmacokinetics, Safety and Tolerability of Oral Semaglutide in Subjects With Various Degrees of Impaired Renal Function Compared to Subjects With Normal Renal Function
This trial is conducted in Europe.
The aim of the trial is to investigate the pharmacokinetics (the exposure of the trial drug in the body), safety and tolerability of oral semaglutide in subjects with various degrees of impaired renal function compared to subjects with normal renal function.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
71
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 85 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Male or female aged 18-85 years (both inclusive) at the time of signing inform consent
- Subject with normal renal function or renal impairment (mild, moderate, severe or end-stage renal disease requiring dialysis)
- For subject with normal renal function: good general health (as judged by the investigator)
- Body mass index (BMI) 18.5-40.0 kg/m^2 (both inclusive)
Exclusion Criteria:
- Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using adequate contraceptive methods
- History of Crohn's disease, ulcerative colitis, or other inflammatory bowel disease
- Uncontrolled hypertension (defined as systolic blood pressure above or equal to 180 mmHg and/or diastolic blood pressure above or equal to 100 mmHg)
- Any blood draw or donation of blood or plasma in excess of 400 mL within the 3 months preceding the screening visit (Visit 2)
- History of significant drug abuse, or a positive drug test at the screening visit (Visit 2)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Subjects with renal impairment
|
Once daily oral administration of semaglutide formulated with SNAC.
Dose escalation, with 5 days on 5 mg followed by 5 days on 10 mg
|
ACTIVE_COMPARATOR: Subjects with normal renal function
|
Once daily oral administration of semaglutide formulated with SNAC.
Dose escalation, with 5 days on 5 mg followed by 5 days on 10 mg
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Area under the semaglutide plasma concentration time curve
Time Frame: From time 0 to 24 hours after the 10th dosing
|
From time 0 to 24 hours after the 10th dosing
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Maximum observed semaglutide plasma concentration
Time Frame: 0 to 24 hours after the 10th dosing
|
0 to 24 hours after the 10th dosing
|
Area under the SNAC (Sodium N-[8-(2-hydroxybenzoyl) amino] caprylate /salcaprozate sodium) plasma concentration time curve
Time Frame: From time 0 to 24 hours after the 10th dosing
|
From time 0 to 24 hours after the 10th dosing
|
Maximum observed SNAC plasma concentration
Time Frame: 0 to 24 hours after the 10th dosing
|
0 to 24 hours after the 10th dosing
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
December 11, 2013
Primary Completion (ACTUAL)
October 24, 2014
Study Completion (ACTUAL)
October 24, 2014
Study Registration Dates
First Submitted
December 12, 2013
First Submitted That Met QC Criteria
December 12, 2013
First Posted (ESTIMATE)
December 18, 2013
Study Record Updates
Last Update Posted (ACTUAL)
April 19, 2018
Last Update Submitted That Met QC Criteria
April 17, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NN9924-4079
- 2013-000682-36 (EUDRACT_NUMBER)
- U1111-1139-4281 (OTHER: WHO)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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