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Study identifier: NCT06329973 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Fruquintinib in Combination With Sintilimab and CAPEOX as First-line Treatment for G/GEJ Cancer

Condition: Metastatic Gastroesophageal Junction Adenocarcinoma  ·  Sponsor: Henan Cancer Hospital

PhasePhase 1/Phase 2
Planned participants70
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Based on the current status and progress in the treatment of gastric cancer, our center prospectively designed a first-line comprehensive treatment plan for unresectable or postoperative recurrent advanced gastric/gastroesophageal conjoint adenocarcinoma, fruquintinib + sintilimab + oxaliplatin + Capecitabine (CAPEOX), which utilizes the tumor immunomodulation and vascular normalization effects of fruquintinib. While improving the effective perfusion of intravenous chemotherapy with CAPEOX regimen, further combining with PD-1 monoclonal antibody to regulate the immunosuppressive microenvironment and reactivate the anti-tumor immune response of the body. An exploratory dose-climbing trial was designed to evaluate the clinical efficacy and safety of fruquintinib in combination with Sintilimab and CAPEOX in clinical practice. At the same time, changes in genome, pathology and immune microenvironment of tumor-related tissues before and after treatment were observed, and molecular markers related to curative effect were screened to explore the molecular mechanism affecting the curative effect of combination therapy, and further enrichment of therapeutic advantage groups to improve the surgical conversion rate laid the foundation for future large-scale clinical studies

This description comes directly from the study's public registry record.

Talk to the study team

Xiaobing Chen  ·  +8613937100233  ·  zlyychenxb0807@zzu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Henan Cancer HospitalZhengzhou, Henan, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06329973