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OncoMatch/Clinical Trials/NCT06671548

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

Is NCT06671548 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies Relugolix for heavy menstrual bleeding.

Phase 3RecruitingQilu Pharmaceutical Co., Ltd.NCT06671548Data as of Jun 2026Location: China

Treatment: RelugolixThe goal of this clinical trial is to determine the benefit of relugolix 40 milligrams (mg) once a day compared with placebo in heavy menstrual bleeding associated with uterine fibroids. The main question\[s\] it aims to answer are: * the benefit of relugolix 40 mg once daily in women with heavy menstrual bleeding associated with uterine fibroids * the safety of relugolix 40 mg once daily in women with heavy menstrual bleeding associated with uterine fibroids

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Extracted eligibility criteria

Treatments studied

Endocrine / hormonal

Relugolix

Demographics

Female only

Prior therapy

Cannot have received: gonadotropin-releasing hormone (GnRH) agonist or antagonist

Previous treatment with gonadotropin-releasing hormone (GnRH) agonists or GnRH antagonists for uterine fibroids has failed

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06671548 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior gonadotropin-releasing hormone (GnRH) agonist or antagonist disqualifies patients from enrollment.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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