NSCLC Clinical Trial
Official title:
A Randomized, Double-blind, Placebo-controlled, Multi-center Phase III Clinical Trial in Patients With Advanced Non-squamous Non-small Cell Lung Cancer Treated With Fruquintinib
Fruquintinib/Placebo 5 mg, QD, orally administered under fasting conditions for 3 consecutive weeks followed by one-week off to evaluate the survival benefit of patients with advanced non-squamous NSCLC treated with Fruquintinib.
This is a randomized, double-blind, placebo-controlled, multi-center Phase III clinical trial
in patients with advanced non-squamous non-small cell lung cancer (NSCLC) treated with
Fruquintinib who failed 2 lines of systemic chemotherapy or with non-tolerable toxicities.
Approximately 521 subjects will be randomized to Fruquintinib group or placebo group at a
ratio of 2:1. Patients in the two groups can receive supportive treatment.
Randomization will be stratified by EGFR gene status (mutant vs. wild type) and history of
treatment by VEGF inhibitors (yes vs no) .
All subjects will receive study treatment in 4-week cycles: Fruquintinib/placebo for 3
consecutive weeks, and then one week off. Tumor assessment will be performed every 4 weeks in
the first 2 cycles, and every 8 weeks since the 3rd cycle, until disease progression or
death. Subsequent anti-neoplastic treatment and survival status will be followed up after
disease progression.
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