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Completed

NCT Number: NCT01403038

An Open-label Study of the Effects of Elagolix in Adult Premenopausal Females

This is an open-label Phase 1 study in healthy premenopausal females evaluating the effects of different dosing regimens of elagolix on ovarian activity, ovulation, and ovarian reserve and to assess the effect of elagolix on selected endocrine/hormone levels.

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1

Primary location

Site Reference ID/Investigator# 53363, San Juan, Puerto Rico

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About this study

This is an open-label, multiple-dose, Phase 1 study in premenopausal subjects aged 18 years to 40 years, with a history of regular menstrual cycles (24 to 32 days long) and no evidence of significant gynecological disorders. The objective of the study is to determine the effects of different dosing regimens of elagolix on ovulation, ovarian activity, and ovarian reserve. The study consists of 3 periods: a Screening Period of up to 50 days prior to the first dose, a Treatment Period of 3 months duration (Cycles 1-3), and a Follow-up Period of up to 60 days. During the Screening and Treatment menstrual cycles, serial transvaginal ultrasounds and determination of serum levels of luteinizing hormone, follicle-stimulating hormone, estradiol, progesterone, and inhibin B will be performed three times weekly. Subjects will maintain a daily diary of uterine bleeding. Pregnancy testing will be performed frequently throughout the study. Subjects will be required to use nonhormonal dual contraception consistently during the study, and will be counseled on appropriate and effective forms of birth control to promote pregnancy prevention.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Premenopausal female, between 18 and 40 years of age, inclusive - History of regular menstrual cycles - Endocrine and ultrasonographic evidence of ovulation and normal ovulatory cycle during the screening period - Follicle-stimulating hormone level of <35 mIU/mL - Agrees to use required birth control methods during the entire length of participation in the study

Exclusion criteria

  • Screening ultrasound results show a clinically significant gynecological disorder - Surgical history of hysterectomy without oophorectomy, unilateral or bilateral oophorectomy, removal of ovarian cysts - Less than 6 months postpartum or post-lactation at the start of study drug dosing - Pregnant or breast feeding or is planning a pregnancy within the next 12 months - Testosterone concentration >120 ng/dL at screening

Treatment and study plan

Elagolix

Drug

Elagolix Dose Regimen 1 for 84 days

Other names: ABT-620, elagolix sodium

Primary outcomes

  1. Ovulation Classification

    Time frame: During the baseline menstrual cycle and monthly during the treatment cycles 1, 2, and 3 for up to month 3.

    Presence or absence of ovulation

  2. Ovarian Activity

    Time frame: During the baseline menstrual cycle and monthly during the treatment cycles 1, 2, and 3 for up to month 3.

    As measured by the Hoogland and Skouby 6-point ovarian activity grading system

Secondary outcomes

  1. Endocrine Parameters

    Time frame: During the 16 week study period (4 week screening period and 12 week treatment period) for up to month 3

    Estuarial, Progesterone, luteinizing hormone, follicle stimulating hormone

  2. Ovarian Reserve

    Time frame: During the baseline menstrual cycle and monthly during the treatment cycles 1, 2, and 3 for up to month 3.

    Inhibin-B and Antimullerian hormone

  3. Adverse events

    Time frame: All adverse events occurring through the Final Visit will be reported

    All adverse events will be collected by subject self-report and review of laboratory parameters, physical exam. vital sign measurements and electrocardiograms.

  4. Clinical Laboratory Tests

    Time frame: Change from baseline to Cycles 1, 2, and 3 or Final Visit

    Chemistry, hematology, urinalysis

  5. 12-lead Electrocardiogram

    Time frame: Change from baseline to Week 4 and Final Visit

    12-lead Electrocardiogram

  6. Vital Signs

    Time frame: Change from baseline to Cycles 1, 2, and 3 or Final Visit

    Blood pressure, heart rate, temperature

Sponsors and collaborators

Lead sponsor

AbbVie (prior sponsor, Abbott)

Industry

Collaborators

  • Neurocrine Biosciences

Registry information

Official study title

A Phase 1, Open-Label Study of the Effects of Elagolix on Ovarian Activity, Ovulation and Ovarian Reserve in Premenopausal Females

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Jul 27, 2011
Registry last updated
Jan 8, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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