drugset / Trial / NCT00949650

BIBW 2992 (Afatinib) Versus Chemotherapy as First Line Treatment in NSCLC With EGFR Mutation

NCT00949650 ↗

Phase 3 Completed 345 enrolled Boehringer Ingelheim
RandomizedParallel-groupOpen-labelTreatment

Summary

This randomised, open label phase III trial will be performed in patients with adenocarcinoma of the lung with tumours harbouring an Epidermal Growth Factor Receptor activating mutation. The objectives of the trial are to compare the efficacy of single agent BIBW 2992, Arm A, with Pemetrexed/Cisplatin chemotherapy, Arm B, as first line treatment for this group of patients.

Timeline

Start
2009-08-14
Primary completion
2012-02-09
Completion
2017-03-16

Outcome

Met primary endpoint

paper Median PFS was 11.1 months for afatinib and 6.9 months for chemotherapy (hazard ratio [HR], 0.58; 95% CI, 0.43 to 0.78; P = .001). PMID 37235976 ↗

registry analysis (superiority or other test); Afatinib 40 mg vs Pemetrexed/Cisplatin Chemotherapy; p = 0.0002; Hazard Ratio (HR) 0.576 (95% CI 0.426 to 0.778); Regression, Cox NCT00949650 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Afatinib Small molecule 40 mg Oral
Comparator Cisplatin Other / unclassified — Intravenous
Comparator Pemetrexed Small molecule — Intravenous