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Raloxifene

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IDDRUG-RALOXIFENE
TypeDrug
Aliases
EvistaРалоксифен
Statusreviewed 2026-05-18 | pending_clinical_signoff
DiseasesNone declared
SourcesSRC-NCCN-BCELL-2025 SRC-NCCN-BREAST-2025

Drug Facts

ClassSelective estrogen receptor modulator (SERM)
MechanismBenzothiophene SERM with mixed estrogen-receptor agonist/antagonist activity tissue-specific to tamoxifen: antagonist in breast and uterus (no endometrial agonism — lower endometrial-cancer risk than tamoxifen), agonist in bone (BMD preservation) and lipid metabolism. FDA-approved for postmenopausal osteoporosis and invasive-breast-cancer risk reduction. STAR P-2 trial established non-inferior breast-cancer-prevention efficacy vs. tamoxifen in postmenopausal women with lower endometrial-cancer and VTE risk.
Typical dosingPO: 60 mg once daily with or without food, for 5 years for chemoprevention (per STAR P-2 and NSABP P-2 protocols). Postmenopausal only. Same dose for osteoporosis prevention/treatment. No specific dose adjustment for hepatic/renal impairment but caution in severe.
Ukraine registeredTrue
NSZU reimbursedFalse
Ukraine last verified2026-05-18

Warnings

Notes

STUB — v0.2 prevention-workstream authoring; pending two-Clinical-Co-Lead signoff per CHARTER §6.1 dev-mode. POSTMENOPAUSAL ONLY for breast chemoprevention. Per STAR P-2 (NSABP-P2), raloxifene reduces invasive breast cancer ~38% (vs. ~50% for tamoxifen) with lower endometrial cancer (no agonism) and lower VTE rates. Preferred over tamoxifen in postmenopausal women with intact uterus or VTE-risk profile. Adds osteoporosis benefit. NOT for premenopausal use or DCIS prevention (insufficient data; tamoxifen retains the indication there).

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