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Sevabertinib: First Approval.

Drugs 2026 Vol.86(5) p. 759-764

Keam SJ

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Sevabertinib (HYRNUO), an oral, reversible, small molecule tyrosine kinase inhibitor (TKI) of human epidermal growth factor receptor 2 (HER2) that also shows activity against epidermal growth factor r

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BibTeX ↓ RIS ↓
APA Keam SJ (2026). Sevabertinib: First Approval.. Drugs, 86(5), 759-764. https://doi.org/10.1007/s40265-026-02299-w
MLA Keam SJ. "Sevabertinib: First Approval.." Drugs, vol. 86, no. 5, 2026, pp. 759-764.
PMID 41882473

Abstract

Sevabertinib (HYRNUO), an oral, reversible, small molecule tyrosine kinase inhibitor (TKI) of human epidermal growth factor receptor 2 (HER2) that also shows activity against epidermal growth factor receptor (EGFR), is being developed by Bayer for the treatment of solid tumours with mutations in HER2 or EGFR genes. Sevabertinib is derived from Bayer's strategic research alliance with the Broad Institute of MIT and Harvard. In November 2025, sevabertinib was approved under accelerated approval in the USA for use in adults with locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) whose tumours have HER2 (ERBB2) TK domain (TKD) activating mutations, as detected by an FDA-approved test, and who have received a prior systemic therapy. This article summarizes the milestones in the development of sevabertinib leading to this first approval for the treatment of locally advanced or metastatic NSCLC with HER2 (ERBB2) activating mutations.

MeSH Terms

Humans; Carcinoma, Non-Small-Cell Lung; Lung Neoplasms; Drug Approval; Erb-b2 Receptor Tyrosine Kinases; Protein Kinase Inhibitors; Antineoplastic Agents; ErbB Receptors; Mutation; Carbazoles; United States; United States Food and Drug Administration; Anilides; Quinolines

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