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NCT07384234RecruitingPhase 2

SHR-1701 Combined With Chemotherapy for Gastric or Gastroesophageal Junction Adenocarcinoma With Peritoneal Metastasis

SHR-1701 Combined With Chemotherapy for Gastric or Gastroesophageal Junction Adenocarcinoma With Peritoneal Metastasis: an Exploratory Study

Source: ClinicalTrials.gov · Last updated 23 Jul 2026

Brief summary (registry, in English)

This study is a prospective, randomized, two-cohort trial designed to evaluate the efficacy and safety of two regimens in the treatment of gastric or gastroesophageal junction adenocarcinoma with peritoneal metastasis: SHR-1701 combined with intravenous and intraperitoneal paclitaxel plus S-1, or SHR-1701 combined with CAPOX.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
60 (estimated)
First submitted
26 Jan 2026
Start date
24 Apr 2026
Primary completion date
30 Dec 2028
Lead sponsor
Ruijin Hospital
NCT number
NCT07384234

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 60
  • From 24 Apr 2026 to the primary completion date, 30 Dec 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous history of gastric cancer surgery.
  • Contraindications to surgical treatment or chemotherapy, or poor physical status and organ function precluding major abdominal surgery.
  • Active autoimmune disease within 4 weeks prior to enrollment or a history of autoimmune disease.
  • Significant cardiovascular disease within 6 months prior to enrollment, including unstable angina or myocardial infarction.

Other

  • Known HER2-positive.
  • Presence of distant metastases other than peritoneal metastases (e.g., liver, lung, ovarian, para-aortic lymph node, brain metastases, etc.).

Who the study is looking for

  • Age ≥ 18 years old.
  • Pathologically confirmed gastric or gastroesophageal junction adenocarcinoma (Siewert typeⅡ and type Ⅲ gastroesophageal junction adenocarcinoma are eligible for inclusion).
  • Definitively diagnosed with peritoneal metastasis by exploratory laparoscopy and/peritoneal lavage cytology (CY0P1/CY1P0/CY1P1 are eligible, ovarian metastasis is permitted), and without gastric outlet obstruction or intestinal obstruction.
  • No prior anti-tumor treatment history (including radiotherapy, chemotherapy, targeted therapy, immunotherapy, etc.).
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1.
  • Normal function of major organs.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Changhai Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting
Ruijin Hospital Shanghai Jiaotong University School of Medicine
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.