Your session is about to expire
← Back to Search
Gonadotropin-Releasing Hormone (GnRH) Antagonist
Elagolix + COC for Endometriosis
Verified Trial
Phase 3
Recruiting
Research Sponsored by AbbVie
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Are your menstrual cycles regular, meaning every 21-35 days?
Documented surgical confirmation of endometriosis and associated moderate to severe pain.
Must not have
Are you currently breastfeeding, pregnant, or planning a pregnancy.
You have been diagnosed with PCOS
Timeline
Screening 3 weeks
Treatment Varies
Follow Up month 3
Awards & highlights
Pivotal Trial
Summary
This trial will evaluate the efficacy and safety of elagolix in combination with COC compared to placebo in women with endometriosis.
Who is the study for?
This trial is for adult women who have endometriosis with moderate to severe pain and are suitable candidates for combined oral contraceptives (COCs). They must not be pregnant, breastfeeding, or planning pregnancy until the study ends. Participants should not have had a hysterectomy or oophorectomy, osteoporosis, other metabolic bone diseases, or any chronic pain conditions that could affect their pain assessment.
What is being tested?
The study tests how well elagolix works with COCs compared to a placebo in managing painful periods due to endometriosis. About 800 participants will be randomly assigned to one of three groups: two receiving different treatments and one receiving a placebo. After three months on varied regimens, all participants will receive elagolix with COCs from Month 4 through Month 18.
What are the potential side effects?
Potential side effects include those commonly associated with hormonal contraceptives such as nausea, headaches, mood changes, weight gain and breast tenderness. Elagolix may cause liver issues, bone loss over long-term use and hot flashes.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowExclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ month 3
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~month 3
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Percentage of Responders Based on Dysmenorrhea (DYS) Pain Scale
Secondary study objectives
Percentage of Responders Based on Non-Menstrual Pelvic Pain (NMPP) Pain Scale
Side effects data
From 2021 Phase 4 trial • 82 Patients • NCT0388622013%
HEADACHE
11%
HOT FLUSH
100%
80%
60%
40%
20%
0%
Study treatment Arm
Placebo
Elagolix 150 mg
Awards & Highlights
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
3Treatment groups
Experimental Treatment
Placebo Group
Group I: Double-Blind: Elagolix + COCExperimental Treatment2 Interventions
Participants will receive double-blind elagolix in combination with COC (combined oral contraceptive) on Day 1 for 3 months. At month 4, participants will receive open-label elagolix in combination with COC for 15 months. Participants will be followed-up for up to 12 months.
Group II: Double-Blind: ElagolixExperimental Treatment2 Interventions
Participants will receive double-blind Elagolix on Day 1 for 3 months. At month 4, participants will receive open-label elagolix in combination with COC (combined oral contraceptive) for 15 months. Participants will be followed-up for up to 12 months.
Group III: Double-Blind: PlaceboPlacebo Group3 Interventions
Participants will receive double-blind placebo on Day 1 for 3 months. At month 4, participants will receive open-label elagolix in combination with COC (combined oral contraceptive) for 15 months. Participants will be followed-up for up to 12 months.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Combined Oral Contraceptive
2010
Completed Phase 4
~680
Elagolix
2019
Completed Phase 4
~6190
Find a Location
Who is running the clinical trial?
AbbVieLead Sponsor
1,022 Previous Clinical Trials
519,379 Total Patients Enrolled
ABBVIE INC.Study DirectorAbbVie
443 Previous Clinical Trials
159,865 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am a woman aged between 18 and 49.My doctor thinks I can safely use combined oral contraceptives.I have had surgery that confirmed I have endometriosis with moderate to severe pain.
Research Study Groups:
This trial has the following groups:- Group 1: Double-Blind: Elagolix + COC
- Group 2: Double-Blind: Placebo
- Group 3: Double-Blind: Elagolix
Awards:
This trial has 1 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Female Patient Testimony for trial: Trial Name: NCT04333576 — Phase 3
Share this study with friends
Copy Link
Messenger