Safety of Repeat Doses of IV Serelaxin in Subjects With Chronic Heart Failure
Completed · Phase 2 · Has a placebo group
Conditions studied: Chronic Heart Failure
In brief
The purpose of this study was to assess the safety of repeat doses of serelaxin in chronic heart failure.
Key facts
- Study ID
- NCT01982292
- Run by
- Novartis Pharmaceuticals
- People needed
- 321
- Starts
- 2014-05-01
- Expected to finish
- 2015-09-01
- Last updated by the study team
- 2016-11-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Novartis Investigative Site — Colorado Springs, Colorado, United States
- Novartis Investigative Site — Jacksonville, Florida, United States
- Novartis Investigative Site — South Miami, Florida, United States
- Novartis Investigative Site — Minneapolis, Minnesota, United States
- Novartis Investigative Site — Minneapolis, Minnesota, United States
- Novartis Investigative Site — Chapel Hill, North Carolina, United States
- Novartis Investigative Site — Knoxville, Tennessee, United States
- Novartis Investigative Site — Richmond, Virginia, United States
- Novartis Investigative Site — Geelong, Australia
- Novartis Investigative Site — Melbourne, Australia
- Novartis Investigative Site — Brno-Bohunice, Czech Republic, Czechia
- Novartis Investigative Site — Jihlava, Czechia
- Novartis Investigative Site — Prague, Czechia
- Novartis Investigative Site — Turku, Finland, Finland
- Novartis Investigative Site — Lübeck, Germany, Germany
- Novartis Investigative Site — Hanover, Lower Saxony, Germany
- Novartis Investigative Site — Berlin, State of Berlin, Germany
- Novartis Investigative Site — Berlin, Germany
- Novartis Investigative Site — Dresden, Germany
- Novartis Investigative Site — Frankfurt, Germany
- Novartis Investigative Site — Greifswald, Germany
- Novartis Investigative Site — Grünstadt, Germany
- Novartis Investigative Site — Jena, Germany
- Novartis Investigative Site — Kiel, Germany
- Novartis Investigative Site — Anaheim, California, United States
Full record on ClinicalTrials.gov
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