drugset / Trial / NCT04415853

Study of Larotinib in Unresectable Advanced or Recurrent Esophageal Cancer

NCT04415853

Phase 3 Recruiting 416 enrolled Sunshine Lake Pharma Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a randomized, controlled, multi-center, open trial, unresectable locally advanced or metastatic esophageal squamous cell carcinoma patients that failed at least second-line treatment and overexpressed EGFR were enrolled and randomly assigned to the experimental group and control group at a 1: 1 ratio.,who received Larotinib and the chemotherapy regimen chosen by the investigator (Irinotecan Hydrochloride Injection or Tegafur Gimeracil Oteracil Potassium Capsule),respecitively. Subjects are administered until disease progression assessed by the RECIST V1.1 standard (unless the investigator evaluates that the subject continues to have clinical benefit from continuing treatment, the subject may be allowed to continue treatment), and begins to receive new anti-tumor treatment, unacceptable toxicity, withdrawal of informed consent, or other conditions that meet the criteria for terminating trial treatment / withdrawal from the trial. The research phase of this study is divided into pre-screening period (\~ D-28), screening period (D-28 \~ D-1), treatment period, treatment end visit (± 7 days after the last dose), safety follow-up ( Until 28 ± 7 days after the last dose) and survival follow-up.

Timeline

Start
2021-01-21
Primary completion
2026-08
Completion
2026-12-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Irinotecan Small molecule 180 mg/m2 Intravenous
Subject Larotinib Unknown 350 mg Oral
Comparator S-1 Small molecule 40 mg Oral
Comparator S-1 Small molecule 60 mg Oral

Indications