Investigating the Influence of Omeprazole on the Pharmacokinetics of Oral Semaglutide in Healthy Subjects
Study Details
Study Description
Brief Summary
This trial is conducted in Europe. The aim of this trial is to investigate the influence of omeprazole on the pharmacokinetics (the exposure of the trial drug in the body) of oral semaglutide in healthy subjects.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 1 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Semaglutide
|
Drug: semaglutide
All subjects will be treated for 10 consecutive days including dose escalation, with 5 days on 5 mg oral semaglutide followed by 5 days on 10 mg oral semaglutide.
|
| Experimental: Semaglutide + Omeprazole
|
Drug: semaglutide
All subjects will be treated for 10 consecutive days including dose escalation, with 5 days on 5 mg oral semaglutide followed by 5 days on 10 mg oral semaglutide.
Drug: Omeprazole
Will be given daily with oral semaglutide.
|
Outcome Measures
Primary Outcome Measures
- Area under the semaglutide plasma concentration time curve [From time 0 to 24 hours after the 10th daily dose]
Secondary Outcome Measures
- Area under the SNAC plasma concentration time curve [From time 0 to 24 hours after the 10th daily dose]
- Number of hypoglycaemic episodes [From first dosing (Day 1) to completion of the follow-up visit (Day 43 (± 2 days))]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Male or female age 18-75 years (both inclusive) at time of signing informed consent
-
Body mass index of 18.5-29.9 kg/m^2 (both inclusive)
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A good general health based on medical history, physical examination, and results of vital signs, electrocardiogram and laboratory safety tests performed during the screening visit, as judged by the investigator
Exclusion Criteria:
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Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using adequate contraceptive methods. Female of child bearing potential must use effective methods of birth control for the duration of the trial and for 5 weeks following last dose. Only highly effective methods of birth control are accepted (i.e., one that results in a less than 1% per year failure rate when used consistently and correctly, such as implants, injectables, combined oral contraceptives, and some intrauterine devices)
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History of Crohn's disease, ulcerative colitis, or other inflammatory bowel disease
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Hypertension (defined as sitting systolic blood pressure above or equal to 140 mmHg and/or diastolic blood pressure above or equal to 90 mmHg). If white-coat hypertension is suspected at the screening visit a repeated measurement is allowed
-
Any blood draw in excess of 25 mL in the past month, or donation of blood or plasma in excess of 400 mL within the 3 months preceding screening
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Novo Nordisk Investigational Site | Berlin | Germany | 14050 |
Sponsors and Collaborators
- Novo Nordisk A/S
Investigators
- Study Director: Global Clinical Registry (GCR, 1452), Novo Nordisk A/S
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- NN9924-4141
- 2013-005513-12
- U1111-1151-5077