Efficacy Study of Fedovapagon for Nocturia in Men With Benign Prostatic Hyperplasia (BPH)

Completed · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Nocturia

In brief

This study will investigate the efficacy and safety of fedovapagon in the treatment of nocturia in men with BPH.

Key facts

Study ID

NCT02637960

Run by

Vantia Ltd

People needed

432

Starts

2016-03-01

Expected to finish

2017-08-01

Last updated by the study team

2018-10-31

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Adult males ≥18 years [no upper limit]
• Benign prostatic hyperplasia
• Persistent nocturia despite previous lifestyle modification advice including appropriate fluid management
• Serum sodium not below lower limit of normal prior to randomization
• Provide signed and dated informed consent before any study-specific procedures are conducted.
• Able to comply with the requirements of the study.

Where it is running

• Vantia Investigative Center — Anniston, Alabama, United States
• Vantia Investigative Center — Goodyear, Arizona, United States
• Vantia Investigative Center — Lincoln, California, United States
• Vantia Investigative Center — Murrieta, California, United States
• Vantia Investigative Center — San Diego, California, United States
• Vantia Investigative Center — Aventura, Florida, United States
• Vantia Investigative Center — Bradenton, Florida, United States
• Vantia Investigative Center — Clearwater, Florida, United States
• Vantia Investigative Center — Coral Gables, Florida, United States
• Vantia Investigative Center — DeLand, Florida, United States
• Vantia Investigative Center — Hialeah, Florida, United States
• Vantia Investigative Center — Miami, Florida, United States
• Vantia Investigative Center — Ocala, Florida, United States
• Vantia Investigative Center — Pembroke Pines, Florida, United States
• Vantia Investigative Center — St. Petersburg, Florida, United States
• Vantia Investigative Center — Tampa, Florida, United States
• Vantia Investigative Center — Avon, Indiana, United States
• Vantia Investigative Center — Topeka, Kansas, United States
• Vantia Investigative Center — Wichita, Kansas, United States
• Vantia Investigative Center — Greenbelt, Maryland, United States
• Vantia Investigative Center — Missoula, Montana, United States
• Vantia Investigative Center — Omaha, Nebraska, United States
• Vantia Investigative Center — Englewood, New Jersey, United States
• Vantia Investigative Center — Lawrenceville, New Jersey, United States
• Vantia Investigative Center — Albuquerque, New Mexico, United States

Full record on ClinicalTrials.gov

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