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Brief Title: To Evaluate the Efficacy and Safety of Afatinib for Advanced ALTRK-negative ESCC
Official Title: A Multicenter, Open-label, Randomized, Controlled Phase II Study to Evaluate the Efficacy and Safety of Afatinib Versus Irinotecan as a Second-line and Above Treatment for Advanced ALTRK-negative ESCC
Study ID: NCT05818982
Brief Summary: This is a phase II study to evaluate the effectiveness and safety of Afininib compared to irinotecan in the 3-gene RNA sequencing (ALTRK) negative advanced esophageal squamous squamous carcinoma.
Detailed Description: Participants were assigned to either group A or group B at 2:1 randomization (block randomization). Group A received afatinib (40 mg orally/day) every 6 weeks; Group B received irinotecan (140-180mg/m2 intravenous) every 2 weeks.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Beijing Cancer Hospital, Beijing, China, Beijing, , China
First Hospital of Xiamen University Affiliated Hospital,Xiamen,China, Xiamen, , China
Xinxiang Central Hospital of Henan Province, Xinxiang, China, Xinxiang, , China