A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas

Inclusion Criteria:

• Pre-menopausal women, 18-50 years, inclusive.

• Cyclic abnormal uterine bleeding (heavy or prolonged).

• Menstrual blood loss (MBL) of ≥ 80 mL as measured by the alkaline hematin method inthe first 8 days of menses.

• Minimum of one discrete leiomyoma observable by transvaginal ultrasound.

• Endometrial biopsy without evidence of malignancy or atypical or non-atypicalhyperplasia

Exclusion Criteria:

• History of uterine surgery that would interfere with the study endpoints.

• Known coagulation disorder including bleeding disorder or clotting disorder.

• History of, or current uterine, cervix, ovarian, or breast cancer.

• Alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP),or total bilirubin two times or greater than the upper limit of normal rang