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NCT06730373RecruitingPhase 2

First-line Treatment With RC48 Plus Sintilimab and S-1 in Advanced Gastric Cancer (RCTS2)

A Phase II, Open-Label, Multicenter Trial Comparing Disitamab Vedotin Plus Sintilimab and S-1 With Trastuzumab Plus Chemotherapy ± Sintilimab for First-Line Treatment of HER2-Positive Advanced Gastric or Gastroesophageal Junction Adenocarcinoma (RCTS2)

Source: ClinicalTrials.gov · Last updated 15 Sept 2026

Brief summary (registry, in English)

This is a Phase II, randomized, multicenter, open-label clinical trial designed to compare Disitamab Vedotin plus Sintilimab and S-1 with Trastuzumab plus chemotherapy ± Sintilimab for first-line treatment of HER2-Positive advanced gastric or gastroesophageal junction adenocarcinoma.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
110 (estimated)
First submitted
4 Dec 2024
Start date
17 Oct 2024
Primary completion date
31 Dec 2026
Lead sponsor
Qilu Hospital of Shandong University
NCT number
NCT06730373

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 110
  • From 17 Oct 2024 to the primary completion date, 31 Dec 2026
  • 20 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

  • Has received systematic treatment with Chinese patent medicine or immunomodulatory drugs (including thymosin, interferon, interleukin, except for local use for ascites control) before the first administration within 2 weeks.
  • Clinically significant pleural effusion, pericardial effusion or ascites should be drained for many times within 2 weeks before the first administration of the trial drug;
  • Any major surgery was performed ≤ 28 days before the first trial drug administration;

Other illness

  • Allergy to any trial drug and its excipients, or serious allergy history, or contraindication of the trial drug;
  • Have a history of interstitial lung disease, non-infectious pneumonia, pulmonary fibrosis, acute lung disease, or systemic disease with poor control (including but not limited to diabetes, hypertension, etc.);
  • Have a history of active immune deficiency or autoimmune diseases, including HIV positive test, or have other acquired or congenital immune deficiency diseases, or have a history of organ transplantation or autoimmune diseases;
  • Severe chronic or active infection requires systemic antibacterial, antifungal or antiviral treatment, including tuberculosis infection.Have a history of active tuberculosis infection ≥ 1 year before recruitment should also be excluded, unless proved has been completed appropriate treatment;
  • Has a second clinically detectable primary malignant tumor at the time of recruitment, or there were other malignant tumors in the past 5 years (except for fully treated skin basal cell carcinoma or cervical carcinoma in situ);
  • History of allogeneic stem cell transplantation or organ transplantation;

Other

  • Cardiovascular and cerebrovascular events that are not well controlled;
  • Brain metastasis or leptomeningeal metastasis;

Who the study is looking for

  • Aged18-80 years, gender is not limited;
  • Pathologically confirmed locally advanced gastric or gastroesophageal junction adenocarcinoma that is inoperable or has distant metastasis;
  • HER2-Positive (IHC3+or IHC2+/FISH+) ;
  • Has at least 1 measurable lesion as determined by RECIST 1.1;
  • There is no systematic treatment in the past, or the patient has received neoadjuvant/adjuvant chemotherapy, but the disease progresses or relapses more than 6 months after the end of treatment;
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-1;
  • Adequate organ function;
  • The life expectancy is at least 3 months;

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

Full criteria on ClinicalTrials.gov

Sites (20)

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

SiteCityCountrySite status
Binzhou Medical University Hospital
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BinzhouChinaNot yet recruiting
Shengli Oilfield Central Hospital
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DongyingChinaRecruiting
Shandong Provincial Third Hospital
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JinanChinaRecruiting
Shandong Provincial Hospital Affiliated to Shandong First Medical University
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JinanChinaRecruiting
Shandong Univerisity Qilu Hospital
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JinanChinaRecruiting
Jinan Third People's Hospital
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JinanChinaRecruiting
Affiliated Hospital of Jining Medical College
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JiningChinaRecruiting
Liaocheng People's Hospital
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LiaochengChinaRecruiting
LinYi Cancer Hospital
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LinyiChinaRecruiting
The Affiliated Hospital of Qingdao University
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QingdaoChinaNot yet recruiting
Qilu Hospital of Shandong University (Qingdao)
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QingdaoChinaRecruiting
The Second Affiliated Hospital of Shandong First Medical University
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TaianChinaRecruiting
Taian City Central Hospital
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TaianChinaNot yet recruiting
Tengzhou Central People's Hospital
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TengzhouChinaRecruiting
Weifang Hospital of traditional Chinese Medicine
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WeifangChinaNot yet recruiting
Yantai Yuhuangding Hospital
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YantaiChinaRecruiting
Yantaishan Hospital
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YantaiChinaRecruiting
The First Affiliated Hospital of Zhengzhou University
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ZhengzhouChinaRecruiting
Zibo First People's Hospital
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ZiboChinaRecruiting
Zibo Central hospital
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ZiboChinaRecruiting

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