An open-label study designed to determine the safety, tolerability and pharmacodynamics of CD-NP infusions in heart failure patients.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
24 hr intravenous infusion
To assess the safety and tolerability of CD-NP infusions in patients with heart failure
Time frame: 28 days
To evaluate the effect of CD-NP infusions on urinary flow rate, urinary sodium and potassium excretion
Time frame: 24 hrs
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