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Bazedoxifene/Conjugated Estrogen

University of North Carolina, Chapel Hill · FDA-approved active Small molecule

Bazedoxifene acts as a selective estrogen receptor modulator (SERM) that provides estrogen-like benefits while blocking estrogen effects in breast tissue, combined with conjugated estrogens for menopausal symptom relief.

Bazedoxifene acts as a selective estrogen receptor modulator (SERM) that provides estrogen-like benefits while blocking estrogen effects in breast tissue, combined with conjugated estrogens for menopausal symptom relief. Used for Moderate to severe vasomotor symptoms associated with menopause, Prevention of postmenopausal osteoporosis.

At a glance

Generic nameBazedoxifene/Conjugated Estrogen
Also known asDuavee
SponsorUniversity of North Carolina, Chapel Hill
Drug classSelective Estrogen Receptor Modulator (SERM) combined with Conjugated Estrogens
TargetEstrogen receptor alpha (ERα) and estrogen receptor beta (ERβ)
ModalitySmall molecule
Therapeutic areaWomen's Health / Endocrinology
PhaseFDA-approved

Mechanism of action

Bazedoxifene is a SERM that selectively activates estrogen receptors in bone and the cardiovascular system while antagonizing them in breast tissue, reducing breast cancer risk. When combined with conjugated estrogens, it provides systemic estrogen replacement therapy for menopausal symptoms while the bazedoxifene component offers tissue-selective protection against estrogen-related adverse effects in the breast.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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