The goal of the study is to learn what happens to levels of MK-7602 in a healthy person's body over time. Researchers will compare what happens to MK-7602 in the body when it is given with or without another medicine called efavirenz, and when it is given with or without a meal.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
34
Fortrea Clinical Research Unit Inc ( Site 0001)
Daytona Beach, Florida, United States
Area Under the Concentration-Time Curve from Time 0 to Infinity (AUC0-Inf) of MK-7602
Blood samples will be collected to determine the AUC0-inf of MK-7602.
Time frame: At designated time points (up to 4 weeks)
Area Under the Concentration-Time Curve from Time 0 to 24 hours (AUC0-24hrs) of MK-7602
Blood samples will be collected to determine the AUC0-24hr of MK-7602.
Time frame: At designated time points (up to 4 weeks)
Maximum Plasma Concentration (Cmax) of MK-7602
Blood samples will be collected to determine the Cmax of MK-7602.
Time frame: At designated time points (up to 4 weeks)
Time to Maximum Plasma Concentration (Tmax) of MK-7602
Blood samples will be collected to determine the Tmax of MK-7602.
Time frame: Predose and at designated time points (up to 4 weeks)
Plasma Concentration at 24 Hours (C24) of MK-7602
Blood samples will be collected to determine the C24 of MK-7602.
Time frame: At designated time points (up to 4 weeks)
Apparent Terminal Half-life (t1/2) of MK-7602
Blood samples will be collected to determine the t1/2 of MK-7602.
Time frame: At designated time points (up to 4 weeks)
Number of Participants Who Experience an Adverse Event (AE)
An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. The number of participants who experience an AE will be reported.
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Time frame: Up to approximately 10 weeks
Number of Participants Who Discontinue Study Treatment Due to an AE
An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. The number of participants who discontinue study treatment due to an AE will be reported.
Time frame: Up to approximately 10 weeks
Part 2: AUC0-Inf of MK-7602
Blood samples will be collected to determine the AUC0-inf of MK-7602.
Time frame: At designated time points (up to 4 weeks)
Part 2: AUC0-24hrs of MK-7602
Blood samples will be collected to determine the AUC0-24hr of MK-7602.
Time frame: At designated time points (up to 4 weeks)
Part 2: Cmax of MK-7602
Blood samples will be collected to determine the Cmax of MK-7602.
Time frame: At designated time points (up to 4 weeks)
Part 2: Tmax of MK-7602
Blood samples will be collected to determine the Tmax of MK-7602.
Time frame: Predose and at designated time points (up to 4 weeks)
Part 2: C24 of MK-7602
Blood samples will be collected to determine the C24 of MK-7602.
Time frame: At designated time points (up to 4 weeks)
Part 2: t1/2 of MK-7602
Blood samples will be collected to determine the t1/2 of MK-7602.
Time frame: At designated time points (up to 4 weeks)