Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
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.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on sunvozertinib.