LIBERTY 2: Efficacy & Safety Study of Relugolix in Women With Heavy Menstrual Bleeding Associated With Uterine Fibroids

Completed · Phase 3 · Has a placebo group

Conditions studied: Heavy Menstrual Bleeding, Uterine Fibroid

In brief

The purpose of this study is to determine the benefit of relugolix 40 milligrams (mg) once a day co-administered with estradiol (E2) 1 mg and norethindrone acetate (NETA) 0.5 mg compared with placebo for 24 weeks on heavy menstrual bleeding associated with uterine fibroids.

Key facts

Study ID

NCT03103087

Run by

Myovant Sciences GmbH

People needed

382

Starts

2017-06-14

Expected to finish

2020-09-16

Last updated by the study team

2022-04-20

Who can join

Age: 18 and older, up to 50. Sex: female. Healthy volunteers: not accepted.

Where it is running

• Mesa — Mesa, Arizona, United States
• Tucson — Tucson, Arizona, United States
• Tuscon — Tucson, Arizona, United States
• Canoga Park — Canoga Park, California, United States
• Huntington Beach — Huntington Beach, California, United States
• Long Beach — Long Beach, California, United States
• Los Angeles — Los Angeles, California, United States
• Los Angeles — Los Angeles, California, United States
• Panorama — Panorama City, California, United States
• San Diego — San Diego, California, United States
• Upland — Upland, California, United States
• Denver — Denver, Colorado, United States
• Lakewood — Lakewood, Colorado, United States
• Washington — Washington D.C., District of Columbia, United States
• Aventura — Aventura, Florida, United States
• DeLand — DeLand, Florida, United States
• Ft. Lauderdale — Fort Lauderdale, Florida, United States
• Jupiter — Jupiter, Florida, United States
• Lake City — Lake City, Florida, United States
• Loxahachee — Loxahatchee Groves, Florida, United States
• Miami — Miami, Florida, United States
• Miami — Miami, Florida, United States
• Miami Springs — Miami Springs, Florida, United States
• New Port Richey — New Port Richey, Florida, United States
• Birmingham — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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