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Clinical Trial Details

Trial ID: L3219
Source ID: NCT00972322
Associated Drug: Mk-8245
Title: Pharmacokinetics and Pharmacodynamics of MK-8245 in Participants With Type 2 Diabetes (MK-8245-012)
Acronym:
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT00972322/results
Conditions: Type 2 Diabetes Mellitus
Interventions: DRUG: MK-8245|DRUG: Comparator: placebo
Outcome Measures: Primary: Change From Baseline in the 24-hour Weighted Mean Glucose (WMG), The 24-hour WMG is derived from multiple glucose values collected during both fasting and post-meal periods. A "weighted" rather than a "simple" mean is used to avoid overrepresentation of post-meal glucose values. Blood samples for glucose were collected immediately prior to, and after each meal, and overnight and fasting one hour pre-dose., Baseline and Day 28|Number of Participants Who Experienced Serious or Non-serious Adverse Events, An adverse event (AE) is defined as any unfavorable and unintended sign including an abnormal laboratory finding, symptom or disease associated with the use of a medical treatment or procedure, regardless of whether it is considered related to the medical treatment or procedure, that occurs during the course of the study. A serious AE is any untoward medical occurrence that results in death, is life threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, or is a congenital anomaly/birth defect., Up to Day 31|Number of Participants Discontinuing Study Drug Due to an AE, An adverse event (AE) is defined as any unfavorable and unintended sign including an abnormal laboratory finding, symptom or disease associated with the use of a medical treatment or procedure, regardless of whether it is considered related to the medical treatment or procedure, that occurs during the course of the study., Up to Day 28 |
Sponsor/Collaborators: Sponsor: Merck Sharp & Dohme LLC
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 56
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
Start Date: 2009-08-24
Completion Date: 2010-01-26
Results First Posted: 2014-06-12
Last Update Posted: 2018-09-10
Locations:
URL: https://clinicaltrials.gov/show/NCT00972322