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Study identifier: NCT07181499 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Sequential Chemotherapy With Befotertinib in Non-Small Cell Lung Cancer (NSCLC) Patients With Resistance to Third-Generation EGFR-TKI

Condition: NSCLC · Adjuvant Drug Therapy · EGFR  ·  Sponsor: Betta Pharmaceuticals Co., Ltd.

PhasePhase 2
Planned participants28
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Non-small cell lung cancer (NSCLC) accounts for over 85% of lung cancers. Approximately 30-40% of East Asian adenocarcinoma patients harbor EGFR mutations. Third-generation EGFR-TKIs achieve a median PFS of about 20 months as first-line therapy, but resistance eventually develops. Studies like MARIPOSA-2 confirm that amivantamab combined with chemotherapy ± lazertinib or immunotherapy regimens (ivucitinib/sintilimab + bevacizumab + chemotherapy) can extend median PFS post-resistance from approximately 4 months to 6-8 months. As a third-generation TKI, befitinib has demonstrated PFS of 16-22 months in both first-line and post-T790M mutation settings. This study aims to further evaluate the feasibility and safety of "pemetrexed + carboplatin followed by befotertinib" for patients resistant to third-generation TKIs.

This description comes directly from the study's public registry record.

Talk to the study team

Shaodong Hong  ·  15920527656  ·  hongshd@sysucc.org.cn

Always discuss trial participation with your own doctor first.

Locations (2)

Sun Yat-sen University Cancer CenterGuangzhou, Guangdong, ChinaRecruiting
The Cancer Center of The Fifth Affiliated Hospital of Sun Yat-sen UniversityZhuhai, Guangdong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07181499