About this trial

This study was designed to evaluate the safety and efficacy of fruquintinib plus trastuzumab, and XELOX as first-line treatment for HER2-positive advanced gastric or gastroesophageal junction (GEJ) adenocarcinoma.

Eligibility criteria

Qualifiers

Have fully understood the study and voluntarily signed the informed consent;

18-75 years old (including 18 and 75 years old);

Pathologically determined advanced gastric or gastroesophageal junction adenocarcinoma;

No previous anti-tumor treatment for metastatic diseases;

Disqualifiers

Failure to comply with the study protocol or study procedure;

Previous treatment with vascular endothelial growth factor receptor (VEGFR) inhibitors, chemotherapy or immune checkpoint inhibitors;

Have had other malignancies within the past 5 years, except basal cell or squamous cell carcinoma of the skin after radical surgery, or carcinoma in situ of the cervix;

Known presence of symptomatic central nervous system metastasis or brain metastases;

Trial design

Treatments tested in this trial

  • fruquintinib+trastuzumab + XELOX

Treatment groups

45 Participants
are divided into 1 treatment group

Locations

1
Henan Cancer Hospital (Affiliated Cancer Hospital of Zhengzhou University)210000, ZhengzhouHenan, China

Sponsors and collaborators

Henan Cancer Hospital

Lead sponsor