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Completed Phase 2 Interventional

Endometriosis Trial: Study of NBI-56418 in Endometriosis

ClinicalTrials.gov ID: NCT00109512

Public ClinicalTrials.gov record NCT00109512. 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 30, 2026, 7:54 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 II, Randomized, Double-Blind, Placebo-Controlled Study of NBI-56418 in Endometriosis

Brief summary

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

This is a Phase II, multicenter, randomized, double-blind, placebo-controlled, parallel-group study with subjects randomized to one of three treatment groups, placebo, 75 mg and 150 mg in a 1:1:1 ratio. Study drug was administered once daily for 12 weeks. After the last dose at the end of Week 12, follow-up continued every 4 weeks for 12 weeks.

Study identification

NCT ID
NCT00109512
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Abbott
Industry
Enrollment
76 participants

Conditions and interventions

Conditions

Interventions

Drug

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
Apr 2005 (Type not available)
Primary completion
Jun 2006 (Actual)
Completion
Jun 2006 (Actual)
Last update posted
Feb 22, 2012

2005 – 2006

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
Site Reference ID/Investigator# 56266 Phoenix Arizona 85032 —
Site Reference ID/Investigator# 55210 San Diego California 92103 —
Site Reference ID/Investigator# 55214 San Ramon California 94566 —
Site Reference ID/Investigator# 56267 Clearwater Florida 33759 —
Site Reference ID/Investigator# 56270 Champaign Illinois 61820 —
Site Reference ID/Investigator# 56273 Chicago Illinois 60612 —
Site Reference ID/Investigator# 56269 Oak Brook Illinois 60523 —
Site Reference ID/Investigator# 56271 Peoria Illinois 61615 —
Site Reference ID/Investigator# 56272 Louisville Kentucky 40291 —
Site Reference ID/Investigator# 55213 Winston-Salem North Carolina 27103 —
Site Reference ID/Investigator# 55211 Arlington Texas 76012 —
Site Reference ID/Investigator# 56268 Sandy City Utah 84070 —
Site Reference ID/Investigator# 56274 Richmond Virginia 23294 —
Site Reference ID/Investigator# 55212 Virginia Beach Virginia 23451 —
Site Reference ID/Investigator# 56275 Spokane Washington 99204 —

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 NCT00109512, 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 Feb 22, 2012 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00109512 live on ClinicalTrials.gov.

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