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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT03201419

Public ClinicalTrials.gov record NCT03201419. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 1:47 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomised, Double-blind, Placebo-controlled, Response-adaptive Dose-finding Trial Investigating the Efficacy, Safety and Tolerability of Oral Doses of FE 201836, With Desmopressin Orally Disintegrating Tablet as a Benchmark, During 12 Weeks of Treatment for Nocturia Due to Nocturnal Polyuria in Adults

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this trial was 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

Study identification

NCT ID
NCT03201419
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
302 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 27, 2017 (Actual)
Primary completion
Oct 31, 2019 (Actual)
Completion
Oct 31, 2019 (Actual)
Last update posted
Mar 2, 2022

2017 – 2019

United States locations

U.S. sites
43
U.S. states
17
U.S. cities
38
Facility City State ZIP Site status
Achieve Clinical Research, LLC Birmingham Alabama 35216 —
Coastal Clinical Research, an AMR company Mobile Alabama 36608 —
Clinical Trials Research Lincoln California 95648 —
Tri Valley Urology Medical Group Murrieta California 92562 —
San Diego Clinical Trials San Diego California 92120 —
Advanced Rx Clinical Research Group, Inc. Westminster California 92683 —
Downtown Women's Health Care Denver Colorado 80209 —
Genitourinary Surgical Consultants, P.C. Denver Colorado 80220 —
South Florida Medical Research Aventura Florida 33180 —
Women's Medical Research Group, LLC Clearwater Florida 33759 —
Tampa Bay Medical Research, Inc. Clearwater Florida 33761 —
Clinical Research of South Florida Coral Gables Florida 33134 —
Avail Clinical Research, LLC DeLand Florida 32720 —
Finlay Medical Research Corp Greenacres City Florida 33467 —
Pharmax Research Clinic Miami Florida 33126 —
Doctors Research Institute Corporation Miami Florida 33145 —
Sanitas Research Miami Florida 33155 —
Bayside Clinical Research LLC New Port Richey Florida 34655 —
Pines Care Research Center, Inc Pembroke Pines Florida 33026 —
Clinical Research Center of Florida Pompano Beach Florida 33060 —
Meridien Research, Inc. St. Petersburg Florida 33709 —
American Health Network of Indiana, LLC Avon Indiana 46123 —
American Health Network of Indiana, LLC Greenfield Indiana 46140 —
Bay State Clinical Trials, Inc. Watertown Massachusetts 02472 —
Beyer Research Kalamazoo Michigan 49009 —
Remedica LLC Rochester Michigan 48307 —
Quality Clinical Research Center, Inc. Omaha Nebraska 68114 —
Clinical Research Consortium, an AMR company Las Vegas Nevada 89119-5190 —
Mid Hudson Medical Research, PLLC New Windsor New York 12553 —
Premier Medical Group of the Hudson Valley, PC Poughkeepsie New York 12601 —
American Health Research, Inc. Charlotte North Carolina 28207 —
Medication Management, LLC Greensboro North Carolina 27408 —
Peters Medical Research High Point North Carolina 27262 —
PMG Research of Raleigh, LLC Raleigh North Carolina 27609 —
PMG Research of Wilmington, LLC Wilmington North Carolina 28401 —
HWC Women's Research Center Englewood Ohio 45322 —
NECCR Primacare Research, LLC Providence Rhode Island 02908 —
Coastal Carolina Research Center, Inc Mt. Pleasant South Carolina 29464 —
PMG Research of Charleston, LLC Mt. Pleasant South Carolina 29464 —
MCA Research - Partner Houston Texas 77079 —
Ericksen Research & Development, LLC Clinton Utah 84015 —
Advanced Research Institute Ogden Utah 84405 —
Clinical Research Associates of Tidewater, an AMR company Norfolk Virginia 23507 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03201419, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 2, 2022 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03201419 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →