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 |
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
55
sites
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