| Trial ID: | L2537 |
| Source ID: | NCT00567112
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| Associated Drug: |
10 Mg Mk-0941 Dfc (Fasted)
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| Title: |
Study to Evaluate the Pharmacokinetics & Food Effect of MK-0941 in Adults With Type 2 Diabetes (MK-0941-009)
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| Acronym: |
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| Status: |
COMPLETED
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| Study Results: |
YES
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| Results: |
https://ClinicalTrials.gov/show/NCT00567112/results
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| Conditions: |
Type 2 Diabetes Mellitus
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| Interventions: |
DRUG: 10 mg MK-0941 DFC (fasted)|DRUG: 10 mg MK-0941 OCT (after meal)|DRUG: 10 mg MK-0941 OCT (before meal)|DRUG: 10 mg MK-0941 OCT (fasted)
|
| Outcome Measures: |
Primary: Area Under the Curve (AUC)(0-∞) for Oral Compressed Tablet (OCT) (Fasted) and Dry Filled Capsule (DFC) (Fasted), From study drug administration to 72 hours post-administration|Maximum Concentration (Cmax) for OCT (Fasted) and DFC (Fasted), From study drug administration to 72 hours post-administration|Time to Reach Cmax (Tmax) for OCT (Fasted) and DFC (Fasted), From study drug administration to 72 hours post-administration|Half Life (t½) for OCT (Fasted) and DFC (Fasted), From study drug administration to 72 hours post-administration | Secondary: AUC(0-∞) for OCT (Fasted) and OCT (After Meal), From study drug administration to 72 hours post-administration|Cmax of OCT (Fasted) and OCT (After Meal), From study drug administration to 72 hours post-administration|Tmax for OCT (Fasted) and OCT (After Meal), From study drug administration to 72 hours post-administration|t1/2 for OCT (Fasted) and OCT (After Meal), From study drug administration to 72 hours post-administration
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| Sponsor/Collaborators: |
Sponsor: Merck Sharp & Dohme LLC
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| Gender: |
ALL
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| Age: |
ADULT, OLDER_ADULT
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| Phases: |
PHASE1
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| Enrollment: |
18
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| Study Type: |
INTERVENTIONAL
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| Study Designs: |
Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: NONE|Primary Purpose: TREATMENT
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| Start Date: |
2007-11
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| Completion Date: |
2008-04
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| Results First Posted: |
2012-09-05
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| Last Update Posted: |
2015-03-23
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| Locations: |
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| URL: |
https://clinicaltrials.gov/show/NCT00567112
|