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Elagolix for Fertility Enhancement Clinical Trial

Elagolix for Fertility Enhancement Clinical Trial (EFFECT)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04039204
Acronym
EFFECT
Enrollment
10
Registered
2019-07-31
Start date
2022-01-15
Completion date
2023-08-09
Last updated
2024-07-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis, Unexplained Infertility

Brief summary

Studies suggest that undiagnosed endometriosis results in poor reproductive outcomes in the setting of In Vitro Fertilization and Embryo Transfer (IVF-ET). Biomarkers that predict endometriosis including B-cell lymphoma (BCL6) and Sirtuin 1 (SIRT1) are associated with reduced pregnancy rates following IVF-ET. Treatment with gonadotropin releasing hormone (GnRHr) receptor agonists (leuprolide acetate depot) has been shown to improve pregnancy rates following embryo transfer (ET). In this randomized controlled trial, a new generation GnRHr antagonist, elagolix, will be compared to oral contraceptives (OCPs) for suppression of suspected endometriosis prior to ET. Both groups will receive two months of treatment prior to frozen embryo transfer of a single euploid embryo. Outcomes will include pregnancy rate, miscarriage rate and ongoing and live birth rate following treatment. Patients experiencing unanticipated problems or who experience adverse events such that they do not tolerate the treatment they are assigned, will be allowed to discontinue treatment and be provided the opportunity to use the other treatment if they so choose. The outcomes of such cycles would be collected separately and included as observational data only and not included in the randomized data analysis. Alternatively, they can simply drop out of the study and resume medical therapy as appropriate or pursue frozen embryo transfer as previously planned.

Detailed description

Although meta-analyses have not demonstrated an effect of endometriosis on IVF outcomes, most women with endometriosis undergoing IVF have not been diagnosed or treated for their disease. Recent evidence suggests that biomarkers for endometriosis predict IVF failure and miscarriage. Further suppression of endometriosis prior to IVF has been shown to dramatically improve pregnancy rates in unexplained infertility with suspected endometriosis. Elagolix (Orilissa) is a new generation FDA approved orally active GnRHr antagonist that is rapidly reversible, for the treatment of endometriosis and pelvic pain. There have been no studies on the efficacy of elagolix for the treatment of endometriosis-associated infertility. Given the recent study in Fertility and Sterility demonstrating IVF outcome prediction using BCL6 as a biomarker for the presence of endometriosis and subsequent preliminary data showing benefit using surgery and GnRH agonist therapy, there is adequate rationale to examine the use of the orally active, non-peptide compound (elagolix) for estrogen suppression prior to frozen embryo transfer in women who test positive for BCL6 and an associated protein, SIRT1. In this multi-central randomized controlled trial (RCT), the EFFECT Trial, the investigators plan to recruit 100 subjects with prior unexplained IVF failure with positive endometrial BCL6/SIRT1 expression. To qualify all subjects will need to have a preimplantation genetic testing (PGT-A) tested euploid embryo and intentions to undergo frozen embryo transfer. Subjects will be randomized to receive elagolix (200 mg BID) or OCPs for 2 months prior to standardized FET. Primary study outcomes will be pregnancy outcome.

Interventions

DRUGElagolix

This orally active, reversible GnRH antagonist will be used to suppress endometriosis by lowering estrogen levels for 2 months prior to FET

Oral contraceptive prescribed by physician.

Sponsors

University of North Carolina, Chapel Hill
CollaboratorOTHER
Stanford University
CollaboratorOTHER
Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 42 Years
Healthy volunteers
No

Inclusion criteria

* Anti-Mullerian Hormone (AMH) \> 0.5 and \< 10 * At least 1 euploid embryo for transfer * Prior endometrial biopsy showing elevated BCL6 and SIRT1 expression * Endometrial thickness \> 5.9 and \< 14 mm

Exclusion criteria

* Uterine fibroids \> 4 cm (intramural) * Polycystic ovary syndrome (Rotterdam criteria) * Ovarian failure and donor eggs or oocytes * Positive lupus anticoagulant or positive anti-cardiolipin antibody testing * Diabetes mellitus (Type I or II) * Untreated hypothyroidism * Untreated hyperprolactinemia * BMI \<17 or \> 35 * Uncorrected uterine anomaly

Design outcomes

Primary

MeasureTime frame
Number of Live BirthsMonth 9

Secondary

MeasureTime frameDescription
Number of Miscarriagesweek 15The number of subjects with a first trimester pregnancy loss
Number of Viable Pregnancies12 to 15 weeks

Other

MeasureTime frameDescription
Inflammation Measurementsweek 15nanostring arrays for both miRNAs and inflammation biomarkers

Countries

United States

Participant flow

Participants by arm

ArmCount
Elagolix
Elagolix will be dosed at the higher dose used in pelvic pain trials, 200 mg twice a day for 2 months. Elagolix: This orally active, reversible GnRH antagonist will be used to suppress endometriosis by lowering estrogen levels for 2 months prior to FET
5
Oral Contraceptives (Ortho Cyclen)
Elagolix will be compared to a less potent standard commonly used prior to IVF or embryo transfer, namely estrogen containing birth control pills. Ortho Cyclen: Oral contraceptive prescribed by physician.
5
Total10

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyWithdrawal by Subject02

Baseline characteristics

CharacteristicElagolixTotalOral Contraceptives (Ortho Cyclen)
Age, Continuous36.9699175 years
STANDARD_DEVIATION 3.894399758
34.44094 years
STANDARD_DEVIATION 4.236217486
32.417758 years
STANDARD_DEVIATION 3.606106781
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants1 Participants1 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
5 Participants9 Participants4 Participants
Region of Enrollment
United States
5 participants10 participants5 participants
Sex: Female, Male
Female
5 Participants10 Participants5 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 50 / 5
other
Total, other adverse events
0 / 52 / 5
serious
Total, serious adverse events
0 / 50 / 5

Outcome results

Primary

Number of Live Births

Time frame: Month 9

ArmMeasureValue (NUMBER)
ElagolixNumber of Live Births3 live births
Oral Contraceptives (Ortho Cyclen)Number of Live Births1 live births
Secondary

Number of Miscarriages

The number of subjects with a first trimester pregnancy loss

Time frame: week 15

Population: Out of three participants who had embryo transfers in Ortho Cyclen arm, two had viable pregnancies. One of those two had a live birth and one of those two had a miscarriage. So only two participants were analyzed in the Ortho Cyclen arm for this outcome.

ArmMeasureValue (NUMBER)
ElagolixNumber of Miscarriages2 miscarriages
Oral Contraceptives (Ortho Cyclen)Number of Miscarriages1 miscarriages
Secondary

Number of Viable Pregnancies

Time frame: 12 to 15 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
ElagolixNumber of Viable Pregnancies5 Participants
Oral Contraceptives (Ortho Cyclen)Number of Viable Pregnancies2 Participants
Other Pre-specified

Inflammation Measurements

nanostring arrays for both miRNAs and inflammation biomarkers

Time frame: week 15

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026