PROVERA (medroxyprogesterone acetate) by Pfizer is (mpa) inhibits the secretion of gonadotropins which primarily prevents follicular maturation and ovulation and causes thickening of cervical mucus. First approved in 1959.
Drug data last refreshed 2d ago
PROVERA (medroxyprogesterone acetate) is a synthetic progestin oral tablet approved in 1959 that inhibits gonadotropin secretion to prevent follicular maturation and ovulation. It is indicated for contraception, endometrial cancer/hyperplasia, menopause symptoms, osteoporosis, menorrhagia, prostate cancer, endometriosis, and several other conditions. The drug works by thickening cervical mucus and suppressing reproductive hormones across multiple therapeutic domains.
As an LOE-approaching mature product with minimal Part D spending, PROVERA team size is likely small and focused on managed care defense rather than growth initiatives.
(MPA) inhibits the secretion of gonadotropins which primarily prevents follicular maturation and ovulation and causes thickening of cervical mucus. These actions contribute to its contraceptive effect.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Study to Evaluate the Pharmacokinetics (PK) of Medroxyprogesterone Acetate Following an Injection of TV-46046 in Healthy Women of Reproductive Age
Clinical Study of Depo Provera Comparing Lay Health Workers and Clinically-trained Health Workers
Comparative Bioavailability of Two Injectable Suspension Formulations of Medroxyprogesterone Acetate+Estradiol Cypionate
Study to Evaluate Suppression of Ovulation and Pharmacokinetics of Medroxyprogesterone Acetate Following Administration of TV-46046 in Women With Ovulatory Cycle
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moWorking on PROVERA offers limited growth opportunity as a legacy, generic-exposed small-molecule with minimal clinical development pipeline. Roles focus on managing decline, defending remaining market share against generics, and optimizing reimbursement—suitable for professionals seeking stable, defensive brand management experience rather than launch or growth roles.