The purpose of the current study is to assess the safety and tolerability of intravenous tonapofylline.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
420
IV
IV
Assess the safety andtolerability of intravenous tonapofylline, when added to standard therapy in subjects hospitalized with ADHF and renal insufficiency.
Time frame: 0-60 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Huntsville, Alabama, United States
Unnamed facility
Mobile, Alabama, United States
Unnamed facility
Fort Smith, Arkansas, United States
Unnamed facility
Beverly Hills, California, United States
Unnamed facility
Chula Vista, California, United States
Unnamed facility
Mission Viejo, California, United States
Unnamed facility
Monterey Park, California, United States
Unnamed facility
Oceanside, California, United States
Unnamed facility
Redondo Beach, California, United States
Unnamed facility
San Diego, California, United States
...and 179 more locations