The primary objective of the study is to assess the safety and tolerability of IV administration of CD-NP and the dose relationship of CD-NP on improvement of clinical symptoms and renal function in ADHF patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
77
Infusion of CD-NP at one of up to 6 doses or placebo
Unnamed facility
Los Angeles, California, United States
Unnamed facility
Torrance, California, United States
Unnamed facility
Jacksonville, Florida, United States
The occurence of hypotensive events, clinical symptoms, and renal function change with CD-NP infusion.
Time frame: Up to 72 hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Miami Beach, Florida, United States
Unnamed facility
Chicago, Illinois, United States
Unnamed facility
Iowa City, Iowa, United States
Unnamed facility
Detroit, Michigan, United States
Unnamed facility
Minneapolis, Minnesota, United States
Unnamed facility
The Bronx, New York, United States
Unnamed facility
Houston, Texas, United States
...and 11 more locations