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NCT06247956Active, not recruitingPhase 2

Study of SHR-8068 Combined With Adebrelimab and Platinum-containing Chemotherapy in the Treatment of Advanced Gastric and Esophageal Cancer

A Randomized, Open, Multicenter Phase II Clinical Study of SHR-8068 Combined With Adebrelimab and Platinum-containing Chemotherapy in the First-line Treatment of Advanced Gastric and Esophageal Cancer

Source: ClinicalTrials.gov · Last updated 3 Sept 2025

Brief summary (registry, in English)

Objective response rate (ORR) was evaluated to evaluate the efficacy of SHR-8068 combined with adebrelimab and platinum-containing chemotherapy in first-line treatment of advanced gastric and esophageal cancer.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
153 (actual)
First submitted
30 Jan 2024
Start date
11 Mar 2024
Primary completion date
30 Dec 2025
Lead sponsor
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
NCT number
NCT06247956

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 153
  • From 11 Mar 2024 to the primary completion date, 30 Dec 2025
  • 1 site 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

  • Untreated (radiation or surgery) central nervous system metastasis, or accompanied by meningeal metastasis, spinal cord compression, etc.;
  • Previous or co-existing malignant neoplasms;
  • People who have previously received an organ transplant;
  • Known allergic reactions to adebrelimab or other monoclonal antibodies or investigational drugs;

Other illness

  • The presence of any active or known autoimmune disease;
  • Have clinical symptoms or diseases of the heart that are not well controlled;

Other

  • Her2-positive patients;
  • Uncontrolled pleural effusion, pericardial effusion, or peritoneal effusion with clinical symptoms;

Who the study is looking for

  • Volunteer to join the clinical study, and sign the informed consent, compliance is good, can cooperate with follow-up;
  • Aged 18-75 at the time of signing the informed consent;
  • Histologically or cytologically confirmed, unresectable, advanced or recurrent/metastatic adenocarcinoma of the gastric or gastroesophageal junction, or unresectable or recurrent/metastatic esophageal squamous cell carcinoma without radical chemoradiation;
  • At least one measurable lesion consistent with RECIST v1.1;
  • ECOG PS score: 0-1;
  • The organ function level is good;

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Chinese PLA General Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

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