Assess the pharmacokinetics, safety, and tolerability of a single dose of BMS-986177 in participants with normal renal function and moderate to severe renal impairment.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
24
Oral Suspension
Clinical Pharmacology Of Miami Inc.
Miami, Florida, United States
Clinical Pharmacology of Miami LLC
Miami, Florida, United States
Orlando Clinical Research Center
Orlando, Florida, United States
Maximum observed plasma concentration (Cmax)
Measured by plasma concentration
Time frame: Up to 5 days
AUC from time zero to time of last quantifiable concentration (AUC (0-T))
Summary measures of PK parameters
Time frame: Up to 5 days
AUC from time zero extrapolated to infinite time (AUC (INF))
Summary measures of PK parameters
Time frame: Up to 5 days
Incidence of Adverse Events (AEs)
Safety and tolerability as measured by incidence of AEs
Time frame: Up to 5 days
Incidence of Serious Adverse Events ( SAEs)
Safety and tolerability as measured by incidence of SAEs
Time frame: Up to 30 days
Change from baseline in electrocardiogram findings
Measured by investigator assessment
Time frame: Up to 5 days
Change from baseline in physical examination findings
Measured by investigator assessment
Time frame: Up to 5 days
Change from baseline in clinical laboratory test findings
Measured by investigator assessment
Time frame: Up to 5 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.