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NCT04756037 · ClinicalTrials.gov registry record · Phase 3

Study of the Safety and Contraceptive Efficacy of Relugolix Combination Therapy in Women With Uterine Fibroids or Endometriosis Who Are at Risk for Pregnancy

A Phase 3 study of Contraception, sponsored by Sumitomo Pharma Switzerland.

Active
Registry status
Phase 3
Development phase
1,020
Enrollment target
20
Study locations

NCT04756037 is a Phase 3 study of Contraception that is active but no longer recruiting, run by Sumitomo Pharma Switzerland. The registered enrollment target is 1,020 participants, above the 440-participant average among 72 other Contraception trials with a reported enrollment target (132% higher). The trial reports 20 study locations across 4 states.

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The verdict

NCT04756037, a Phase 3 study of Contraception, is active but no longer recruiting, sponsored by Sumitomo Pharma Switzerland.

ACTIVE NOT RECRUITING
Registry status
Phase 3
Development phase
1,020 participants
Enrollment target
20
Study locations

Study Summary

The purpose of this study is to assess the contraceptive efficacy of relugolix combination therapy.

Conditions Studied

Interventions

  • DRUG Relugolix Combination Therapy

Study Locations (20)

California

  • Burbank - Burbank
  • Canoga Park - Canoga Park
  • Encinitas - Encinitas
  • Gardena - Gardena
  • Lancaster - Lancaster
  • Long Beach - Long Beach
  • Long Beach - Long Beach
  • Palo Alto - Palo Alto
  • Sacramento - Sacramento
  • San Diego - San Diego
  • San Fernando - San Fernando
  • Valley Village - Valley Village
  • West Covina - West Covina

Arizona

  • Chandler - Chandler
  • Mesa - Mesa
  • Peoria - Peoria
  • Phoenix - Phoenix

Colorado

  • Aurora - Aurora
  • Greenwood Village - Greenwood Village

Alabama

  • Mobile - Mobile

Trial Details

FieldValue
Enrollment Target 1,020 participants
Start Date 2021-03-18
Est. Completion 2026-02
Phase Phase 3

Sponsor

Sumitomo Pharma Switzerland

13 total trials

What the Registry Record Tells You About NCT04756037

The ClinicalTrials.gov registry entry for NCT04756037 describes a study currently listed as active not recruiting, categorized as Phase 3. The registered enrollment target is 1,020 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 440-participant average among 72 other Contraception trials with a reported enrollment target (132% higher). The listed sponsor is Sumitomo Pharma Switzerland, which has 13 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Contraception appearing as the primary indexed condition, and to 1 intervention - of which Relugolix Combination Therapy is the first listed.

NCT04756037 reports 20 study locations spanning 4 distinct geographic areas - top geographies include California, Arizona, Colorado.

Frequently Asked Questions

What is clinical trial NCT04756037 about?

NCT04756037 is a clinical study titled "Study of the Safety and Contraceptive Efficacy of Relugolix Combination Therapy in Women With Uterine Fibroids or Endometriosis Who Are at Risk for Pregnancy". The purpose of this study is to assess the contraceptive efficacy of relugolix combination therapy.

What is the current status of trial NCT04756037?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 1,020 participants. The study started on 2021-03-18. Estimated completion is 2026-02.

What conditions does trial NCT04756037 study?

This clinical trial studies the following conditions: Contraception.

What interventions are being tested in trial NCT04756037?

The interventions under investigation include: Relugolix Combination Therapy (DRUG).

Who is sponsoring clinical trial NCT04756037?

This trial is sponsored by Sumitomo Pharma Switzerland, which has 13 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04756037 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.