A study to compare a 48-hour continuous infusion of conivaptan in subjects with mild and moderate liver impairment versus subjects with normal liver function
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Masking
NONE
Enrollment
26
intravenous
Unnamed facility
Miami, Florida, United States
Measure PK and protein binding of conivaptan
Time frame: 5 days
Measure tolerability of conivaptan
Time frame: 5 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.