Contraceptive Efficacy and Safety of NOMAC-E2 Combined Oral Contraceptive
About the study
The purpose of this study is evaluating Contraceptive Efficacy and Safety of NOMAC-E2 Combined Oral Contraceptive in Premenopausal Females Aged 14 to 35 Years (Inclusive).
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
- Postmenarcheal, premenopausal female aged 14 to 35 years (inclusive)
- At risk for pregnancy (including heterosexual vaginal intercourse at least once a month and not sterilized).
- No desire for pregnancy within 1 year following screening and is not intending to use any other form of contraception
- Good physical and mental health
- History of regular menstrual cycles prior to the use of any hormonal contraceptive.
- Able and willing to adhere study procedures
EXCLUSION CRITERIA
Exclusion Criteria:
- Current known or expected pregnancy
- History of subfertility or infertility
- Less than 2 normal menstrual cycles following recent pregnancy of gestational age
- Breastfeeding within 2 months of study drug start
- Known HIV infection
- Untreated gonorrhea, chlamydia, or trichomonas
- abnormal PAP within timeline of standard of care guidelines
- Unexplained/unresolved abnormal vaginal bleeding
- Presence/history of VTE, ATE, transient ischemic attack, angina pectoris, or claudication
- Higher risk for VTE
- Uncontrolled or severe hypertension
- Severe dyslipoproteinemia
- History of migraine with aura or focal neurological symptoms
- Diabetes mellitus (with either end-organ involvement or >20 years duration)
- Multiple cardiovascular risk factors
- History of pancreatitis associated with severe hypertriglyceridemia
- Presence/history of clinically significant liver disease
- History of malabsorptive surgical procedures
- History of malignancy in last 5 years
- Presence/history of meningioma
- Disease that may worsen under hormonal treatment
- Presence/history of severe depression (unless currently stable and asymptomatic)
- Known allergy/sensitivity to NOMAC-E2
- Drug or alcohol abuse/dependence in last 2 years
- Clinically relevant abnormal lab result at screening
- Expected use of other contraceptive medications or medications that induce liver enzymes during study
- Used another investigational drug within 2 months of study drug start
Study Locations
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How to Apply
Contact the study center to learn if this study is a good match for you.
Study’s details
Contition
Contraception
Age (in years)
14 - 35
Phase
Phase 3
Participants needed
1878
Est. Completion Date
Mar 31, 2024
Treatment type
Interventional
Sponsor
Organon and Co
ClinicalTrials.gov identifier
NCT05264506
Study number
OG-8175A-023
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