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Insights Into Vepdegestrant (ARV-471): The First-in-Class Estrogen Receptor Proteolysis-Targeting Chimera Approaching Food and Drug Administration Approval for Breast Cancer.

ChemMedChem 2026 Vol.21(6) p. e202501111

Tang C, Tian B, Zhang B, Zhang Y, Ke C, Chen M, Wei M, Wang W, Deng X, Zhang Q, Wang M, Xia J, He M, Liang C, Tian L

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Vepdegestrant (ARV-471) is an orally bioavailable, proteolysis-targeting chimera (PROTAC)-based estrogen receptor (ER) degrader and is among the most clinically advanced ER-targeting PROTAC degraders,

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APA Tang C, Tian B, et al. (2026). Insights Into Vepdegestrant (ARV-471): The First-in-Class Estrogen Receptor Proteolysis-Targeting Chimera Approaching Food and Drug Administration Approval for Breast Cancer.. ChemMedChem, 21(6), e202501111. https://doi.org/10.1002/cmdc.202501111
MLA Tang C, et al.. "Insights Into Vepdegestrant (ARV-471): The First-in-Class Estrogen Receptor Proteolysis-Targeting Chimera Approaching Food and Drug Administration Approval for Breast Cancer.." ChemMedChem, vol. 21, no. 6, 2026, pp. e202501111.
PMID 41866773

Abstract

Vepdegestrant (ARV-471) is an orally bioavailable, proteolysis-targeting chimera (PROTAC)-based estrogen receptor (ER) degrader and is among the most clinically advanced ER-targeting PROTAC degraders, identified through a rational medicinal chemistry optimization campaign. It is being developed as an oral small-molecule endocrine therapy for advanced or metastatic ER-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer, with particular relevance for tumors harboring ESR1 mutations. On June 6, 2025, Arvinas and Pfizer submitted a New Drug Application (NDA) for vepdegestrant to the U.S. Food and Drug Administration (FDA), representing an important step in the clinical translation of PROTAC technology. This review summarizes the design, synthesis, degradation mechanism, preclinical pharmacology, and clinical development of vepdegestrant and discusses the broader implications and future prospects of oral PROTAC-based ER degraders in breast cancer therapy.

MeSH Terms

Humans; Breast Neoplasms; Proteolysis; Female; United States Food and Drug Administration; United States; Drug Approval; Antineoplastic Agents; Receptors, Estrogen; Estrogen Receptor alpha; Animals; Molecular Structure

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