drugset / Trial / NCT03779191

Alectinib in Combination With Bevacizumab in ALK Positive NSCLC

NCT03779191

NaSingle-groupOpen-labelTreatment

Summary

This single-arm, open-label, phase II clinical study aims to evaluate the progression-Free Survival (PFS) of the combination of Alectinib plus Bevacizumab in untreated and first and second-line chemotherapy failed subjects with stage IIIB/IV or recurrent disease after receiving radiation therapy or surgical resection. The main question to be answered is: Whether the combination of Alectinib plus Bevacizumab will improve PFS in untreated and previously treated subjects with advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) and positive ALK translocation. Participants will be treated with Alectinib and Bevacizumab every three weeks until disease progression, unacceptable toxicity, or patient withdrawal of consent.

Timeline

Start
2020-04-08
Primary completion
2022-08-01
Completion
2022-10-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Alectinib Small molecule 600 mg Oral
Subject Bevacizumab Monoclonal antibody 15 mg/kg Intravenous