Relugolix, a novel oral gonadotropin-releasing hormone antagonist, in the treatment of pain symptoms associated with uterine fibroids: a randomized, placebo-controlled, phase 3 study in Japanese women

Fertil Steril. 2019 Nov;112(5):922-929.e2. doi: 10.1016/j.fertnstert.2019.07.013. Epub 2019 Oct 6.

Abstract

Objective: To investigate the efficacy and safety of the oral gonadotropin-releasing hormone receptor antagonist, relugolix, in patients experiencing uterine fibroid-associated pain.

Design: Phase 3, multicenter, randomized, double-blind, placebo-controlled study.

Setting: Medical centers.

Patient(s): Premenopausal Japanese women (N = 65) experiencing moderate-to-severe uterine fibroid-associated pain with a maximum Numerical Rating Scale (NRS) score of ≥4 were randomized and completed the study.

Intervention(s): Once-daily 40 mg relugolix (n = 33) or placebo (n = 32) for 12 weeks.

Main outcome measure(s): Primary end point: proportion of patients with a maximum NRS score of ≤1 during the 28-day period before the final dose of study drug. Secondary end points: proportion of patients with no pain (NRS = 0) and percentage of days without pain during the 28-day period before the final dose of study drug; adverse events.

Result(s): More patients receiving relugolix versus placebo achieved a maximum NRS score of ≤1 during the 28-day period before the final dose of study drug (57.6% vs. 3.1%). Similarly, more patients receiving relugolix versus placebo achieved a maximum NRS score of 0 (48.5% vs. 3.1%) and experienced more days without pain (96.4% vs. 71.4%). More patients receiving relugolix versus placebo experienced treatment-emergent adverse events (TEAEs; 87.9% vs. 56.3%); however, the rate of treatment discontinuation was low and not different between groups. Most TEAEs were mild to moderate in intensity. TEAEs (≥10%) included hot flush, metrorrhagia, hyperhidrosis, and menorrhagia, consistent with relugolix's mechanism of action, and viral upper respiratory tract infection.

Conclusion(s): Relugolix improved uterine fibroid-associated pain and was well tolerated.

Clinical trial registration numbers: NCT02655224.

Japic clinical trial information: JapicCTI-163127.

Keywords: Gonadotropin-releasing hormone receptor antagonist; pain; randomized controlled trial; relugolix; uterine fibroids.

Publication types

  • Clinical Trial, Phase III
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Adult
  • Double-Blind Method
  • Female
  • Gonadotropin-Releasing Hormone / antagonists & inhibitors*
  • Humans
  • Japan / epidemiology
  • Leiomyoma / diagnosis
  • Leiomyoma / drug therapy*
  • Leiomyoma / epidemiology*
  • Middle Aged
  • Pelvic Pain / diagnosis
  • Pelvic Pain / drug therapy*
  • Pelvic Pain / epidemiology*
  • Phenylurea Compounds / administration & dosage*
  • Pyrimidinones / administration & dosage*
  • Treatment Outcome

Substances

  • Phenylurea Compounds
  • Pyrimidinones
  • relugolix
  • Gonadotropin-Releasing Hormone

Associated data

  • ClinicalTrials.gov/NCT02655224
  • JapicCTI/JapicCTI-163127