This study is evaluating the Pharmacokinetics of MNTX in healthy control subjects and in patients with mild, moderate, or severe renal impairment who do not require hemodialysis.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
32
Progenics Pharmaceuticals, Inc.
Tarrytown, New York, United States
Peak Plasma Concentration (Cmax) of MNTX in patients with impaired renal function compared to healthy subjects
To compare the PK of MNTX administered subcutaneously as a single dose in patients with impaired renal function with the PK of MNTX administered to healthy subjects.
Time frame: 6 days
Peak time of maximum concentration (Tmax) of MNTX in patients with impaired renal function compared to healthy subjects
To compare the PK of MNTX administered subcutaneously as a single dose in patients with impaired renal function with the PK of MNTX administered to healthy subjects.
Time frame: 6 days
Area under the plasma concentration (AUC) of MNTX in patients with impaired renal function compared to healthy subjects
To compare the PK of MNTX administered subcutaneously as a single dose in patients with impaired renal function with the PK of MNTX administered to healthy subjects.
Time frame: 6 days
Percent of dose excreted in urine of MNTX in patients with impaired renal function compared to healthy subjects
To compare the PK of MNTX administered subcutaneously as a single dose in patients with impaired renal function with the PK of MNTX administered to healthy subjects.
Time frame: 6 days
Urinary clearance of MNTX in patients with impaired renal function compared to healthy subjects
To compare the PK of MNTX administered subcutaneously as a single dose in patients with impaired renal function with the PK of MNTX administered to healthy subjects.
Time frame: 6 days
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