This study will investigate the efficacy and safety of the monophasic combined oral contraceptive (COC) containing 2.5 mg NOMAC and 1.5 mg E2 in healthy fertile Indian women.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Oral tablet with daily release of 2.5 mg
Daily release of 1.5 mg
Number of In-treatment Pregnancies
Time frame: Day 1 of Treatment Cycle 1 Through Day 28 of Treatment Cycle 13, plus up to 2 additional days (Study Days 1-366)
Number of Participants Experiencing an Adverse Event (AE) or Serious AE
Time frame: "From Visit 1 up to 30 days after the last dose of study medication (up to Study Day 394).
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