The primary purpose of the study is to determine the pharmacokinetics (PK) following a single oral dose administration of brensocatib, safety, and tolerability of brensocatib when administered to participants with impaired renal function and in healthy participants.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
28
Oral tablet
USA002
Orlando, Florida, United States
USA003
Tampa, Florida, United States
USA001
San Antonio, Texas, United States
Area Under the Plasma Concentration Time Curve (AUC) of Brensocatib
Pharmacokinetics of brensocatib following a single dose will be assessed in participants with renal impairment and in healthy participants.
Time frame: Pre-dose and at multiple timepoints post-dose on Days 1 to 14
Maximum Observed Plasma Concentration (Cmax) of Brensocatib
Time frame: Pre-dose and at multiple timepoints post-dose on Days 1 to 14
Time to Reach Maximum Observed Plasma Concentration (Tmax) of Brensocatib
Time frame: Pre-dose and at multiple timepoints post-dose on Days 1 to 14
Number of Participants who Experienced at Least one Adverse Event (AE)
Determination of the safety and tolerability of a single dose of brensocatib in participants with impaired renal function and in healthy participants.
Time frame: Up to Day 14
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