| Trial ID: | L6377 |
| Source ID: | NCT02161588
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| Associated Drug: |
Semaglutide
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| Title: |
A Trial to Assess the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Oral Semaglutide in Healthy Male Japanese and Caucasian Subjects
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| Acronym: |
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| Status: |
COMPLETED
|
| Study Results: |
NO
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| Results: |
|
| Conditions: |
Diabetes|Diabetes Mellitus, Type 2|Healthy
|
| Interventions: |
DRUG: semaglutide|DRUG: placebo
|
| Outcome Measures: |
Primary: Area under the semaglutide plasma concentration-time curve, During a dosing interval (0-24 hours) at steady state | Secondary: Maximum observed semaglutide plasma concentration, During a dosing interval (0-24 hours) at steady state|Number of treatment emergent adverse events (TEAEs) recorded, From the time of first dosing (Day 1) until completion of the follow-up visit (Days 119-126)
|
| Sponsor/Collaborators: |
Sponsor: Novo Nordisk A/S
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| Gender: |
MALE
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| Age: |
ADULT
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| Phases: |
PHASE1
|
| Enrollment: |
48
|
| Study Type: |
INTERVENTIONAL
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| Study Designs: |
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
|
| Start Date: |
2014-06
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| Completion Date: |
2014-11
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| Results First Posted: |
|
| Last Update Posted: |
2014-12-03
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| Locations: |
Tokyo, 130-0004, Japan
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| URL: |
https://clinicaltrials.gov/show/NCT02161588
|