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Terminated Phase 2 Interventional Results available

The Safety and Efficacy of Gefapixant (AF-219/MK-7264) in Female Participants With Interstitial Cystitis /Bladder Pain Syndrome (MK-7264-005)

ClinicalTrials.gov ID: NCT01569438

Public ClinicalTrials.gov record NCT01569438. 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 20, 2026, 1:49 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 Four-Week, Double-Blind, Placebo-Controlled, Randomized, Multicenter Study Evaluating the Safety and Efficacy of AF-219 in Female Subjects With Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS)

Brief summary

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

The purpose of this study is to assess the efficacy of gefapixant (AF-219/MK-7264) in female participants with moderate to severe pain associated with interstitial cystitis/bladder pain syndrome (IC/BPS) after 4 weeks of treatment.

Study identification

NCT ID
NCT01569438
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
107 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Apr 13, 2012 (Actual)
Primary completion
May 1, 2014 (Actual)
Completion
May 14, 2014 (Actual)
Last update posted
Aug 17, 2020

2012 – 2014

United States locations

U.S. sites
41
U.S. states
19
U.S. cities
40
Facility City State ZIP Site status
Afferent Investigative Site Glendale Alabama 85306 —
Afferent Investigative Site Homewood Alabama 35209 —
Afferent Investigative Site Mobile Alabama 36608 —
Afferent Investigative Site Phoenix Arizona 85018 —
Afferent Investigative Site Glendora California 91741 —
Afferent Investigative Site Murrieta California 91741 —
Afferent Investigative Site San Diego California 92120 —
Afferent Investigative Site San Diego California 92123 —
Afferent Investigative Site Farmington Connecticut 06032 —
Afferent Investigative Site New Britain Connecticut 06052 —
Afferent Investigative Site Boynton Beach Florida 33472 —
Afferent Investigative Site Plantation Florida 33317 —
Afferent Investigative Site Coeur d'Alene Idaho 83814 —
Afferent Investigative Site Idaho Falls Idaho 83404 —
Afferent Investigative Site Meridian Idaho 83642 —
Afferent Investigative Site Shreveport Louisiana 71106 —
Afferent Investigative Site Annapolis Maryland 21401 —
Afferent Investigative Site Ann Arbor Michigan 48109 —
Afferent Investigative Site Grand Rapids Michigan 49503 —
Afferent Investigative Site Kalamazoo Michigan 49009 —
Afferent Investigative Site Royal Oak Michigan 48073 —
Afferent Investigative Site Voorhees Township New Jersey 08043 —
Afferent Investigative Site Albuquerque New Mexico 87109 —
Afferent Investigative Site Brooklyn New York 11215 —
Afferent Investigative Site Hyde Park New York 11040 —
Afferent Investigative Site Greenville North Carolina 27834 —
Afferent Investigative Site Salisbury North Carolina 28144 —
Afferent Investigative Site Winston-Salem North Carolina 27103 —
Afferent Investigative Site Cincinnati Ohio 45212 —
Afferent Investigative Site Cleveland Ohio 44109 —
Afferent Investigative Site Tiffin Ohio 43351 —
Afferent Investigative Site Zanesville Ohio 43701 —
Afferent Investigative Site Bala-Cynwyd Pennsylvania 19004 —
Afferent Investigative Site Lancaster Pennsylvania 17604 —
Afferent Investigative Site Myrtle Beach South Carolina 29572 —
Afferent Investigative Site Dallas Texas 75390 —
Afferent Investigative Site Fort Worth Texas 76104 —
Afferent Investigative Site Houston Texas 77062 —
Afferent Investigative Site Irving Texas 75062 —
Afferent Investigative Site Salt Lake City Utah 84124 —
Afferent Investigative Site Virginia Beach Virginia 23462 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01569438, 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 Aug 17, 2020 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01569438 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →