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Completed Phase 3 Interventional

SPIRIT 2: Efficacy and Safety Study of Relugolix in Women With Endometriosis-Associated Pain

ClinicalTrials.gov ID: NCT03204331

Public ClinicalTrials.gov record NCT03204331. 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 21, 2026, 9:02 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

SPIRIT 2: An International Phase 3 Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study to Evaluate Relugolix Administered With and Without Low-Dose Estradiol and Norethindrone Acetate in Women With Endometriosis-Associated Pain

Brief summary

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

The purpose of this study is to determine the benefit and safety of relugolix 40 milligrams (mg) once daily, co-administered with low-dose estradiol (E2) and norethindrone acetate (NETA) compared with placebo for 24 weeks, on dysmenorrhea and on nonmenstrual pelvic pain.

Study identification

NCT ID
NCT03204331
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Myovant Sciences GmbH
Industry
Enrollment
623 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 50 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
Nov 1, 2017 (Actual)
Primary completion
Apr 1, 2020 (Actual)
Completion
May 31, 2021 (Actual)
Last update posted
Jun 28, 2021

2017 – 2021

United States locations

U.S. sites
41
U.S. states
21
U.S. cities
39
Facility City State ZIP Site status
Andalusia Andalusia Alabama 36420 —
Washington DC Washington D.C. District of Columbia 20036 —
Aventura Aventura Florida 33180 —
Deland DeLand Florida 32720 —
Hialeah Hialeah Florida 33012 —
Hialeah Hialeah Florida 33016 —
Margate Margate Florida 33063 —
Miami Miami Florida 33176 —
Port St. Lucie Port Saint Lucie Florida 34952 —
Tampa Tampa Florida 33606 —
Atlanta Atlanta Georgia 30312 —
Idaho Falls Idaho Falls Idaho 83404 —
Park Ridge Park Ridge Illinois 60068 —
Lafayette Lafayette Indiana 47905 —
Covington Covington Louisiana 70433 —
Marrero Marrero Louisiana 70072 —
Towson Towson Maryland 21204 —
Saginaw Saginaw Michigan 48602 —
St. Louis St Louis Missouri 63141 —
Omaha Omaha Nebraska 68124 —
Albuquerque Albuquerque New Mexico 87102 —
New York New York New York 10038 —
New Bern New Bern North Carolina 28562 —
Akron Akron Ohio 44313 —
Columbus Columbus Ohio 43231 —
Columbus Columbus Ohio 43235 —
Franklin Franklin Ohio 45005 —
Columbia Columbia South Carolina 29201 —
Spartanburg Spartanburg South Carolina 29301 —
Chattanooga Chattanooga Tennessee 37404 —
Beaumont Beaumont Texas 77702 —
Corpus Christi Corpus Christi Texas 78412 —
Dallas Dallas Texas 75231 —
Fort Worth Fort Worth Texas 76104 —
Houston Houston Texas 77054 —
Irving Irving Texas 75062 —
San Antonio San Antonio Texas 78258 —
Sugar Land Sugar Land Texas 77479 —
Pleasant Grove Pleasant Grove Utah 84062 —
Salt Lake City Salt Lake City Utah 84102 —
Virginia Beach Virginia Beach Virginia 23502 —

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 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03204331, 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 28, 2021 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03204331 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →