Safety and Efficacy Pre-Menopausal Women With Heavy Uterine Bleeding and Uterine Fibroids



Status:Completed
Conditions:Cervical Cancer, Women's Studies
Therapuetic Areas:Oncology, Reproductive
Healthy:No
Age Range:20 - 49
Updated:5/27/2013
Start Date:September 2011
End Date:April 2014
Contact:Janine North, BS
Email:janine.north@AbbVie.com
Phone:847-938-1999

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Phase 2a Proof Of Concept Study to Evaluate the Safety and Efficacy of Elagolix in Pre-Menopausal Women With Heavy Uterine Bleeding and Uterine Fibroids


The purpose of this proof-of-concept study is to determine whether elagolix (ABT-620) is
safe and effective in the treatment of pre-menopausal women, 20 to 49 years of age, with
heavy uterine bleeding associated with uterine fibroids. The effect of elagolix (ABT-620) on
uterine size, fibroid size, and bleeding associated with uterine fibroids will be assessed
versus placebo, and in combination with add-back therapy.


Inclusion Criteria:

- Subject is a pre-menopausal female ≥ 20 years of age.

- Subject has a diagnosis of uterine fibroids documented by a Pelvic Ultrasound.

- Subject has a history of regular menstrual cycles between 24 to 35 days.

- Subject has heavy uterine bleeding associated with uterine fibroids.

Exclusion Criteria:

- Subject has had a myomectomy, uterine artery embolization, endometrial ablation or
high intensity focused ultrasound for fibroid destruction within 1 year prior to
randomization or any history of endometrial ablation.

- Subject has a history of osteoporosis or other metabolic bone disease.

- Subject shows evidence of clinically significant hematological, renal, endocrine,
pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric (including
depression), or neurologic diseases or any uncontrolled medical illness such as
uncontrolled type 2 diabetes.

- Subject has a history of clinically significant condition(s) including but not
limited to:

- Endometriosis

- Epilepsy or seizures

- Type 1 diabetes

- Any cancer (except basal cell carcinoma of the skin), including breast or
ovarian cancer or subject has taken any systemic cancer chemotherapy
We found this trial at
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