Last updated on June 2019

A Trial to Investigate Efficacy Safety and Tolerability of FE 201836 for Nocturia Due to Nocturnal Polyuria in Adults


Brief description of study

The purpose of this trial is to investigate the efficacy, safety and tolerability of different oral doses of FE 201836, with desmopressin as a benchmark, during 12 weeks of treatment for nocturia due to nocturnal polyuria in adults

Clinical Study Identifier: NCT03201419

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Green Acres, FL United States
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New Port Richey, FL United States
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Pembroke Pines, FL United States
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Pompano Beach, FL United States
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Saint Petersburg, FL United States
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Kalamazoo, MI United States
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Rochester, MI United States
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New Windsor, NY United States
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Charlotte, NC United States
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Medication Management, LLC

Greensboro, NC United States
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Peters Medical Research

High Point, NC United States
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PMG Research of Wilmington, LLC

Wilmington, NC United States
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HWC Women's Research Center

Englewood, OH United States
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Providence, RI United States
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Mount Pleasant, SC United States
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Mount Pleasant, SC United States
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MCA Research - Partner

Houston, TX United States
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UZ Antwerpen

Edegem, Belgium
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Leuven, Belgium
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Ultra-Med Inc.

Pointe-Claire, QC Canada
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Recruitment Status: Open


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