Study of the Contraceptive Efficacy and Safety of a NOMAC-E2 Combined Oral Contraceptive (COC)(P06448)
Status: | Completed |
---|---|
Conditions: | Contraception |
Therapuetic Areas: | Reproductive |
Healthy: | No |
Age Range: | Any |
Updated: | 2/4/2013 |
Start Date: | November 2012 |
End Date: | July 2014 |
Contact: | Toll Free Number |
Phone: | 1-888-577-8839 |
A Phase III, Randomized, Open-label, Active-controlled, Multicenter Trial to Study the Contraceptive Efficacy and Safety of the Commercial Batch of Oral Tablets of MK-8175A (Nomegestrol Acetate - 17ß-estradiol) in Healthy, Sexually-active Women Aged 18-50 Years
The purpose of this study is to assess the contraceptive efficacy of a nomegestrol acetate +
17ß-estradiol (NOMAC-E2) combined oral contraceptive (COC) in healthy, sexually-active
American women at risk for pregnancy. Vaginal bleeding patterns of women taking NOMAC-E2
will be assessed and compared to those of women taking a norethisterone acetate + ethinyl
estradiol (NETA-EE) COC. The safety of NOMAC-E2 will also be assessed.
Participants will be randomized to receive either NOMAC-E2 or NETA-EE in a 3:1 ratio.
Inclusion Criteria:
- Sexually active woman, at risk for pregnancy and in need of contraception
- Not planning to use other contraceptive methods (including barrier methods [e.g.,
condoms]) than the study drug, during the study
- Willing to use a COC for 12 months (13 cycles)
- Body mass index (BMI) of ≥ 18 and < 38 kg/m^2
- Good physical and mental health
- Willing to complete an electronic diary on a daily basis for the duration of the
study
Exclusion Criteria:
- Current smoker and age of > 35 years
- Presence or history of either venous thromboembolic diseases (deep vein thrombosis
[DVT], pulmonary embolism) or arterial thromboembolic diseases (myocardial
infarction, stroke)
- History of migraine with focal neurological symptoms
- Diabetes mellitus with vascular involvement
- Less than two weeks of full remobilization from prolonged immobilization, major
surgery, any surgery to the legs, or major trauma
- Severe hypertension
- Severe abnormal lipoproteins in the blood
- Pancreatic dysfunction
- Presence of history of severe liver disease or liver tumors
- Known or suspected sex steroid-influenced malignancies (e.g., of the genital organs
or the breasts)
- Undiagnosed vaginal bleeding
- Known or suspected pregnancy
- Current or history of abuse of alcohol or drugs (e.g., laxatives)
- Abnormal cervical smear at screening
- Before spontaneous menstruation has occurred following a delivery or abortion
- Breastfeeding or has been breastfeeding within 2 months prior to start of treatment
- Use of any investigational drugs and/or participation in any other clinical trial
within 2 months prior to start of treatment
- Use of any of the following prohibited medications within 2 months prior to start of
treatment and/or will need to continue these medications: sex hormones (other than
pre-treatment non-injectable contraceptives), injectable hormonal contraception,
phenytoin, barbiturates, primidone, bosentan, carbamazepine, topiramate, felbamate,
rifampicin, ritonavir, nevirapine, efavirenz, griseofulvin, herbal remedies
containing St. John's wort (Hypericum perforatum)
We found this trial at
87
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