Drug intelligence / Profile preview

sunvozertinib

Development stage
Approved
Lead developer
Dizal Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

Sunvozertinib is an oral, irreversible, mutant-selective **epidermal growth factor receptor** tyrosine kinase inhibitor developed by Dizal for **non-small cell lung cancer** driven primarily by **EGFR exon 20 insertion mutations**. It was rationally designed to inhibit a broad range of EGFR mutant forms while sparing wild-type EGFR, and preclinical and clinical reports also describe activity in other EGFR-mutant settings and exploratory activity in **HER2 exon 20 insertion** disease. Public sources and the provided trial/publication context identify sunvozertinib under the development code **DZD9008**; it received approval in China in 2023 and accelerated approval in the United States in 2025 for previously treated advanced or metastatic NSCLC with EGFR exon 20 insertion mutations after platinum-based chemotherapy. The drug is being studied across multiple WU-KONG trials in later-line, first-line, combination, and earlier-stage NSCLC settings, and global rights were licensed by AstraZeneca from Dizal in 2026.

Brand names
Zegfrovy舒沃哲
Other names
sunvozertinib舒沃替尼
02

Targets

ERBB2 (Erb-b2 receptor tyrosine kinase 2)EGFR (Epidermal growth factor receptor)ERBB4 (Erb-b2 receptor tyrosine kinase 4)

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