Researchers are studying MK-8527, a new medicine for preventing HIV-1 (human immunodeficiency virus type 1) infection and want to learn if MK-8527 can be given together with rifampin. Rifampin is commonly used to treat people with latent tuberculosis infection (LTBI). The main goal of this study is to learn what happens to MK-8527 in the body over time when given with and without the medication rifampin in participants with LTBI.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
14
Area Under the Concentration-Time Curve From Time Zero to Infinity (AUC0-inf) of MK-8527
Blood samples will be collected to determine the AUC0-inf of MK-8527 in plasma.
Time frame: At designated time points (up to approximately 2 weeks)
Area Under the Concentration-Time Curve From Time Zero to Last Quantifiable Concentration (AUC0-last) of MK-8527
Blood samples will be collected to determine AUC0-last of MK-8527 in plasma.
Time frame: At designated time points (up to approximately 2 weeks)
Area Under the Concentration-Time Curve From Time Zero to 336 Hours (AUC0-336) of MK-8527
Blood samples will be collected to determine AUC0-336 of MK-8527 in plasma.
Time frame: At designated time points (up to approximately 2 weeks)
Maximum Plasma Concentration (Cmax) of MK-8527
Blood samples will be collected to determine Cmax of MK-8527 in plasma.
Time frame: At designated time points (up to approximately 2 weeks)
Time to Maximum Plasma Concentration (Tmax) of MK-8527
Blood samples will be collected to determine Tmax of MK-8527 in plasma.
Time frame: At designated time points (up to approximately 2 weeks)
Terminal Elimination Half-Life (T1/2) of MK-8527
Blood samples will be collected to determine t1/2 of MK-8527 in plasma.
Time frame: At designated time points (up to approximately 2 weeks)
Apparent Clearance (CL/F) of MK-8527
Blood samples will be collected to determine CL/F of MK-8527 in plasma.
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Time frame: At designated time points (up to approximately 2 weeks)
Apparent Volume of Distribution During Terminal Phase (Vz/F) of MK-8527
Blood samples will be collected to determine Vz/F of MK-8527 in plasma.
Time frame: At designated time points (up to approximately 2 weeks)
Number of Participants Who Experience an Adverse Event (AE)
An AE is any untoward medical occurrence in a participant, temporally associated with the use of study treatment, whether or not considered related to the study treatment. The number of participants who experience an AE will be reported.
Time frame: Up to approximately 8 weeks
Number of Participants Who Discontinue Study Treatment Due to an AE
An AE is any untoward medical occurrence in a participant, temporally associated with the use of study treatment, whether or not considered related to the study treatment. The number of participants who discontinue study treatment due to an AE will be reported.
Time frame: Up to approximately 8 weeks