Overview

Safety and Efficacy in Premenopausal Women With Heavy Menstrual Bleeding (HMB) Associated With Uterine Fibroids (UF)

Status:
Completed
Trial end date:
2015-12-01
Target enrollment:
0
Participant gender:
Female
Summary
This is a Phase 2b randomized, double-blind, placebo-controlled study evaluating the safety and efficacy of elagolix alone and in combination with add-back therapy versus placebo on heavy menstrual bleeding in premenopausal women 18 to 51 years of age with uterine fibroids.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
AbbVie
Treatments:
Estradiol
Estradiol 17 beta-cypionate
Estradiol 3-benzoate
Estradiol valerate
Norethindrone
Norethindrone Acetate
Polyestradiol phosphate
Criteria
Inclusion Criteria:

- Subject is pre-menopausal female 18 to 51 years of age at Screening.

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

- Subject has heavy uterine bleeding associated with uterine fibroids.

Exclusion Criteria:

- Subject has had a myomectomy, uterine artery embolization or high intensity focused
ultrasound for fibroid destruction within 6 months prior to Screening or endometrial
ablation within 5 years prior to Screening.

- 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, schizophrenia, bipolar disorder), or neurologic diseases or any
uncontrolled medical illness such as uncontrolled type 2 diabetes. Subject has any
history of attempted suicide.

- Subject has a history of clinically significant condition(s) including but not limited
to: * Symptomatic Endometriosis * Epilepsy or seizures * Type 1 diabetes * Chronic
kidney disease * Any cancer (except treated basal cell carcinoma of the skin),
including breast or ovarian cancer or subject has taken any systemic cancer
chemotherapy