Elagolix
DrugElagolix Dose Regimen 1 for 84 days
Other names: ABT-620, elagolix sodium
NCT Number: NCT01403038
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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Notify Me18 year–40 year
Female
Interventional
Phase 1
Site Reference ID/Investigator# 53363, San Juan, Puerto Rico
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Elagolix Dose Regimen 1 for 84 days
Other names: ABT-620, elagolix sodium
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
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
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
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
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.
Time frame: Change from baseline to Cycles 1, 2, and 3 or Final Visit
Chemistry, hematology, urinalysis
Time frame: Change from baseline to Week 4 and Final Visit
12-lead Electrocardiogram
Time frame: Change from baseline to Cycles 1, 2, and 3 or Final Visit
Blood pressure, heart rate, temperature
AbbVie (prior sponsor, Abbott)
Industry
A Phase 1, Open-Label Study of the Effects of Elagolix on Ovarian Activity, Ovulation and Ovarian Reserve in Premenopausal Females
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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