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Completed Phase 3 Interventional Results available

Safety Study of XP12B in Women With Menorrhagia

ClinicalTrials.gov ID: NCT00113568

Public ClinicalTrials.gov record NCT00113568. 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 Nov 6, 2026, 5:38 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multicenter Study to Evaluate the Safety of XP12B in Women With Heavy Menstrual Bleeding Associated With Menorrhagia

Brief summary

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

The purpose of this study is to evaluate the safety of XP12B in women with heavy menstrual bleeding associated with menorrhagia.

Study identification

NCT ID
NCT00113568
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
784 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 49 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
Jun 2005 (Type not available)
Primary completion
May 2009 (Actual)
Completion
May 2009 (Actual)
Last update posted
Jun 15, 2010

2005 – 2009

United States locations

U.S. sites
59
U.S. states
30
U.S. cities
50
Facility City State ZIP Site status
Investigative Site Birmingham Alabama 35235 —
Investigative Site Mobile Alabama 36608 —
Investigative Site Montgomery Alabama 36106 —
Investigative Site Phoenix Arizona 85032 —
Investigative Site Phoenix Arizona 85035 —
Investigative Site Jonesboro Arkansas 72401 —
Investigative Site Little Rock Arkansas 72205 —
Investigative Site San Diego California 92103 —
Investigative Site San Diego California 92108 —
Investigative Site Colorado Springs Colorado 80909 —
Investigative Site Denver Colorado 80202 —
Investigative Site Fort Myers Florida 33916 —
Investigative Site Miami Florida 33186 —
Investigative Site New Port Richey Florida 34652 —
Investigative Site Ocala Florida 34471 —
Investigative Site Pinellas Park Florida 33781 —
Investigative Site Venice Florida 34292 —
Investigative Site West Palm Beach Florida 33407 —
Investigative Site West Palm Beach Florida 33409 —
Investigative Site Alpharetta Georgia 30005 —
Investigative Site Roswell Georgia 30075 —
Investigative Site Savannah Georgia 31405 —
Investigative Site Savannah Georgia 31406 —
Investigative Site Boise Idaho 83702 —
Investigative Site Champaign Illinois 61820 —
Investigative Site Evansville Indiana 47713 —
Investigative Site Indianapolis Indiana 46250 —
Investigative Site South Bend Indiana 46601 —
Investigative Site Overland Park Kansas 66210 —
Investigative Site Lexington Kentucky 40536 —
Investigative Site Louisville Kentucky 40291 —
Investigative Site Shreveport Louisiana 71103 —
Investigative Site Portage Michigan 49024 —
Investigative Site Chaska Minnesota 55318 —
Investigative Site St Louis Missouri 63110 —
Investigative Site St Louis Missouri 63117 —
Investigative Site St Louis Missouri 63141 —
Investigative Site Billings Montana 59102 —
Investigative Site Omaha Nebraska 68131 —
Investigative Site Las Vegas Nevada 89030 —
Investigative Site Las Vegas Nevada 89128 —
Investigative Site Moorestown New Jersey 08057 —
Investigative Site Albuquerque New Mexico 87102 —
Investigative Site Johnson City New York 13790 —
Investigative Site Charlotte North Carolina 28209 —
Investigative Site Durham North Carolina 27710 —
Investigative Site Winston-Salem North Carolina 27103 —
Investigative Site Cincinnati Ohio 45249 —
Investigative Site Cincinnati Ohio 45267 —
Investigative Site Toledo Ohio 43614 —
Investigative Site Philadelphia Pennsylvania 19104 —
Investigative Site Wexford Pennsylvania 15090 —
Investigative Site Columbia South Carolina 29201 —
Investigative Site Nashville Tennessee 37203 —
Investigative Site Nashville Tennessee 37208 —
Investigative Site Houston Texas 77030 —
Investigative Site Norfolk Virginia 23507 —
Investigative Site Seattle Washington 98105 —
Investigative Site Tacoma Washington 98405 —

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 NCT00113568, 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 Jun 15, 2010 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00113568 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →