Study of the Safety and Efficacy of Ulipristal Acetate (UPA) Used Daily as a Contraceptive

This is an open-label study being conducted at 18 centers. The dose of 10 mg was chosen for
daily continuous use of ulipristal acetate (UPA). The study will enroll approximately 300
subjects to use the UPA for 6 months (182 days). In addition to contraceptive efficacy,
safety, overall acceptability of the product, and the number of bleeding/spotting days will
be assessed.

Inclusion Criteria:

To enroll into the clinical trial, potential subjects must:

1. Be in good general overall health with no chronic medical conditions that result in
periodic exacerbations that require significant medical care.

2. Be women between 18 and 35 years inclusive at the enrollment visit.

3. Have regular menstrual cycles that occur every 21-35 days when not using hormonal
contraception.

a. If subject is postpartum or post-abortal, she must have one menstrual bleed prior
to enrollment.

4. Be seeking contraception, and willing to use the study drug as the only contraception
method during their months of study participation.

5. If using a ring, patch, pill, or implant prior to study treatment, the subject must
discontinue the active hormone at least 4 days, and no more than 7 days, prior to
study drug initiation. Note that for combined oral contraceptive users, placebo pills
are not counted as active hormone.

6. If using a hormonal intrauterine device (IUD) prior to study treatment, the IUD must
be removed prior to study drug initiation; removal and study drug initiation can occur
on the same day, but the subject must refrain from sexual intercourse for 7 days
following IUD removal.

7. If using a copper IUD prior to study treatment, the IUD must be removed prior to study
drug initiation; removal and study drug initiation can occur on the same day. The IUD
removal and study drug initiation must occur during the first 7 days of a spontaneous
menses.

8. If using a non-hormonal contraceptive method (e.g. condoms or withdrawal) prior to
study treatment, drug initiation should occur within the first 7 days of a spontaneous
menses.

9. If the woman has received a long-acting injectable contraceptive (e.g.
depomedroxyprogesterone acetate) during the 10 months prior to screening, she must
have resumed cyclic spontaneous menses (two menstrual bleeds) since last injection.

10. Have a negative urine pregnancy test at the enrollment visit.

11. Have an intact uterus and both ovaries.

12. In the opinion of the investigator, be willing and able to follow all study
requirements, including use of the study product and be willing to record requested
information on a daily diary.

13. Understand and sign an (Institutional Review Board) IRB approved informed consent form
prior to screening activities (including fasting blood draws).

14. Have a diastolic blood pressure (BP) ≤95 mm Hg and systolic BP ≤145 mm Hg after 5
minutes in a sitting position at the enrollment visit. Hypertensive subjects who are
treatment controlled and, in the judgment of the investigator, are good candidates
require a waiver for participation.

15. Have a body mass index (BMI) < 40 kg/m2.

16. Be planning to have at least one act of heterosexual vaginal intercourse each month
during study participation.

17. Be willing to accept an unknown risk of pregnancy during study participation.

Exclusion Criteria:

To enroll into the clinical trial, potential subjects must not:

1. Be women with irregular menstrual cycles defined as a variation in cycle length of
more than 5 days.

2. Be planning pregnancy within their months of study participation.

3. Be currently breast-feeding or within 30 days of discontinuing breast feeding, unless
the subject has already had a menses following discontinuation of breast feeding.

4. Have undiagnosed abnormal genital bleeding.

5. Have known hypersensitivity to the active substance UPA or any of the excipients of
the study treatment.

6. Have a history of endometrial hyperplasia or malignancy.

7. Have abnormal Transvaginal Ultrasound (TVUS) or safety labs done at the screening
visit recognized as clinically significant by the investigator (or medically qualified
designee).

8. Have a previous history of endometrial ablation.

9. Have a previous history of liver disease or screening liver enzyme results more than
three times the upper limit of normal values.

10. Have a known clinically significant Pap test abnormality, as managed by current local
or national guidelines, that would require treatment during study participation.

11. Have any of the following known contraindication to progestin-only oral contraceptive
(OC):

1. History or existing breast cancer, or other hormone sensitive neoplasia;

2. Current or history of ischemic heart disease or stroke while pregnant or taking
birth control pills;

3. Systemic Lupus Erythematosus with positive or unknown antiphospholipid
antibodies;

4. Benign or malignant liver tumors;

5. Severe (decompensated) cirrhosis.

12. Have known or suspected alcoholism or drug abuse.

13. Have known HIV infection.

14. Have an anticipated need for regular condom use as defined as use of at least one
condom per month after enrollment.

15. Have previously participated in the study.

16. Have a current need for exogenous hormones or therapeutic anticoagulants.

17. Have a current or history of deep vein thromboembolic disorder or aortic
thromboembolism, including stroke and myocardial infarction

18. Have a current or past medically diagnosed severe depression, which, in the opinion of
the investigator, could be exacerbated by use of a hormonal contraceptive, unless she
is stable on antidepressant medication.

19. Have concomitant use of medication thought to interact with UPA (per Summary of
Product Characteristics (SPCs)) such as CYP3A4 inducers (rifampin, barbiturates,
carbamazepine, bosentan, felbamate, griseofulvin, oxcarbazepine, phenytoin, St John's
Wort, topiramate).

20. Have concomitant use of moderate or strong CYP3A4 inhibitors as identified by the FDA.
Subjects who begin use of a moderate CYP3A4 inhibitor after study enrollment require a
waiver to continue in the study.

21. Use any medications that can interfere with the metabolism of hormonal contraceptives,
antibiotics that can interfere with metabolism of hormonal contraceptives, or any
drugs designated by the FDA as falling in the Pregnancy and Lactation narrative
subsections (formerly Category D or X medications).

22. Currently participate in any other trial of an investigational medicine or device or
have participated in the three months before start of treatment or be planning to
participate in another clinical trial during this study.

23. Have a history of a bariatric surgery procedure associated with malabsorption.

24. Be planning to undergo major surgery during study participation.

25. Live outside of the catchment area of the study site.

26. Have used UPA, including Ella, within 30 days prior to enrollment and not had a menses
since using UPA.

27. Any site staff member with delegated study responsibilities or a family member of a
site staff member with delegated study responsibilities.