Birth Control

  • sponsor
    Organon & Co
Updated on 19 January 2022


A Phase 3, Open-label, Multi-center, Single-arm Study to Assess ContraceptiveEfficacy and Safety of the Nomegestrol Acetate + 17β-estradiol Combined Oral Contraceptive(OG-8175A) in Premenopausal Females up to 35 Years of Age


  • Condition: Birth Control
  • Clinical Trial Identifier: N/A
  • Sponsor: Organon & Co

Condition Birth Control
Clinical Study IdentifierTX291010
SponsorOrganon & Co
Last Modified on19 January 2022


Yes No Not Sure

Inclusion Criteria

Females age 14 to 35 years
Is at risk for pregnancy (heterosexual vaginal intercourse at least once a month and not sterilized), with a partner who is not known to be subfertile, sterilized, or infertile
Does not desire a pregnancy within 1 year following screening and is not intending to use any other form of contraception (eg, condoms)

Exclusion Criteria

Has a known or suspected pregnancy
Has a history of subfertility or infertility
Has not had at least 2 normal menstrual cycles following a recent pregnancy regardless of gestational age
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What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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