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Completed Phase 3 Interventional Results available

Efficacy and Safety of Gefapixant (MK-7264) in Women With Chronic Cough and Stress Urinary Incontinence (MK-7264-042)

ClinicalTrials.gov ID: NCT04193176

Public ClinicalTrials.gov record NCT04193176. 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 Jun 27, 2026, 2:19 AM 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 Phase 3b Randomized, Double-blind, Placebo Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Gefapixant in Women With Chronic Cough and Stress Urinary Incontinence

Study identification

NCT ID
NCT04193176
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
376 participants

Conditions and interventions

Conditions

Interventions

  • Gefapixant Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
May 9, 2020
Primary completion
Aug 17, 2022
Completion
Sep 1, 2022
Last update posted
Nov 4, 2024

2020 – 2022

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Center for Clinical Trials, LLC ( Site 0021) Paramount California 90723
Health Awareness, Inc. ( Site 0038) Jupiter Florida 33458
Well Pharma Medical Research, Corp. ( Site 0040) Miami Florida 33173
Lenus Research & Medical Group Llc ( Site 0007) Sweetwater Florida 33172
Florida Pulmonary Research Institute, LLC ( Site 0008) Winter Park Florida 32789
Paul A. Shapero, MD ( Site 0037) Bangor Maine 04401
Chesapeake Clinical Research, Inc ( Site 0022) White Marsh Maryland 21162
University of Missouri ENT & Allergy Center ( Site 0010) Columbia Missouri 65201
Alliance for Multispecialty Research, LLC ( Site 0035) Las Vegas Nevada 89119
Albuquerque Clinical Trials ( Site 0019) Albuquerque New Mexico 87102
American Health Research ( Site 0027) Charlotte North Carolina 28277
Clinical Research of Gastonia ( Site 0016) Gastonia North Carolina 28054
PMG Research of Wilmington ( Site 0004) Wilmington North Carolina 28401
Temple University ( Site 0003) Philadelphia Pennsylvania 19140
AAPRI Clinical Research Institute ( Site 0031) Warwick Rhode Island 02886
Diagnostics Research Group ( Site 0013) San Antonio Texas 78229
TPMG Clinical Research ( Site 0025) Newport News Virginia 23606
Tidewater Physician Multispecialty Group, PC ( Site 0028) Williamsburg Virginia 23188
Bellingham Asthma & Allergy ( Site 0006) Bellingham Washington 98225

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 71 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04193176, 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 Nov 4, 2024 · Synced Jun 27, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04193176 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →