The goal of the study is to learn what happens to different oral formulations of tedizolid phosphate (MK-1986) in a healthy person's body over time. Researchers want to know if there is a difference in the absorption and elimination of different oral formulations from the healthy person's body.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
36
Oral administration
Oral administration
Celerion (Site 0001)
Lincoln, Nebraska, United States
Area Under the Concentration-Time Curve from Time 0 to Infinity (AUC0-Inf) of Tedizolid
Blood samples will be collected to determine the AUC0-Inf of tedizolid.
Time frame: At designated time points (up to 3 days postdose)
Area Under the Concentration-Time Curve from Time 0 to the Last Measurable Concentration (AUC0-t) of Tedizolid
Blood samples will be collected to determine the AUC0-t of tedizolid.
Time frame: At designated time points (up to 3 days postdose)
Maximum Plasma Concentration (Cmax) of Tedizolid
Blood samples will be collected to determine the Cmax of tedizolid.
Time frame: At designated time points (up to 3 days postdose)
Time to Maximum Plasma Concentration (Tmax) of Tedizolid
Blood samples will be collected to determine the Tmax of tedizolid.
Time frame: At designated time points (up to 3 days postdose)
Apparent Terminal Half-Life (t1/2) of Tedizolid
Blood samples will be collected to determine the t1/2 of tedizolid.
Time frame: At designated time points (up to 3 days postdose)
Apparent Volume of Distribution of Tedizolid After Nonintravenous Administration (Vd/F)
Blood samples will be collected to determine the Vd/F of tedizolid.
Time frame: At designated time points (up to 3 days postdose)
Oral Clearance (CL/F) of Tedizolid
Blood samples will be collected to determine the CL/F of tedizolid.
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Time frame: At designated time points (up to 3 days postdose)
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.
Time frame: Up to approximately 2 weeks
Number of Participants Who Discontinue Study 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.
Time frame: Up to approximately 2 weeks