drugset / Trial / NCT04206072

D-0316 Versus Icotinib in Patients With Locally Advanced or Metastatic EGFR Sensitising Mutation Positive NSCLC

NCT04206072 ↗

Phase 2/3 Completed 362 enrolled Betta Pharmaceuticals Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

To assess the efficacy and safety of D-0316 versus Icotinib, a standard of care epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI), in patients with locally advanced or Metastatic Non Small Cell Lung Cancer (NSCLC).

Timeline

Start
2019-12-24
Primary completion
2022-07-30
Completion
2025-07-15

Outcome

Met primary endpoint

paper Befotertinib demonstrated superior efficacy compared with icotinib in first-line treatment for patients with EGFR mutation-positive NSCLC. PMID 37244266 ↗

release “贝福替尼组的由独立审查委员会评估的中位无进展生存期为22.1个月(95%CI 17.9-不可估计[NE]),埃克替尼组为13.8个月(95%CI12.4-15.2)(风险比0.49 [95%CI 0.36-0.68], p<0.0001)。” bettapharma.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Befotertinib Small molecule 75 mg Oral
Subject Befotertinib Small molecule 100 mg Oral
Comparator Icotinib Small molecule 125 mg Oral