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Gastric Cancer (Diagnosis)Phase 2NCT07669740

A Study on the Efficacy and Safety of Sintilimab Combined With Ramucirumab and Paclitaxel in the Treatment of Gastric Cancer Patients With Short-term Recurrence After Adjuvant Therapy

A Phase 2 study testing Sintilimab Combined with Ramucirumab and Paclitaxel in people with Gastric Cancer (Diagnosis), run by The First Affiliated Hospital with Nanjing Medical University at 1 site in China.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial summary

To explore the efficacy and safety of sintilimab combined with ramucirumab and paclitaxel in the treatment of advanced gastric cancer patients with short-term recurrence after postoperative adjuvant therapy, and to identify efficacy-related biomarkers to guide subsequent individualized treatment. Read more about this study

Who is it for?
Ages 15 to 75 years
Conditions the study is for
Gastric Cancer (Diagnosis)
What is being tested?
Sintilimab Combined with Ramucirumab and Paclitaxel
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteChina
Study dates
1 Jul 2026to 30 Dec 2028
Phase
Phase 2

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 75 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Age ≥18 years at the time of informed consent.
  • Histologically confirmed gastric or gastroesophageal junction (GEJ)adenocarcinoma.
  • HER2-negative disease, as determined by standard testing methods.
  • Prior D2 radical gastrectomy with R0 resection.
  • Disease recurrence during adjuvant chemotherapy or within 6 months after completion of adjuvant chemotherapy.
  • At least one measurable lesion according to RECIST version 1.1.
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  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
  • Adequate organ and bone marrow function.
  • Life expectancy of at least 3 months.
  • Ability to understand and willingness to sign written informed consent.

Who cannot join

  • Active malignancy within the past 5 years, except for adequately treated in situ carcinoma or other cancers with a negligible risk of recurrence.
  • Prior participation in another investigational drug study within 4 weeks prior to enrollment.
  • Symptomatic central nervous system (CNS) metastases.
  • Active autoimmune disease requiring systemic treatment.
  • Uncontrolled cardiovascular disease or uncontrolled hypertension.
  • History of thromboembolic events or clinically significant bleeding disorders within 6 months prior to enrollment.
  • Active tuberculosis or interstitial lung disease.
  • Known hypersensitivity to monoclonal antibodies or any excipients of the study drug.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

China1 site
  • The First Affiliated Hospital of Nanjing Medical University

    Nanjing, Jiangsu

    Hao Wu, +86 13913855335, whdactor@njmu.edu.cn

Other trials in China

About this study

Official title: A Study on the Efficacy and Safety of Sintilimab Combined With Ramucirumab and Paclitaxel in the Treatment of Gastric Cancer Patients With Short-Term Recurrence After Adjuvant Therapy

To explore the efficacy and safety of sintilimab combined with ramucirumab and paclitaxel in the treatment of advanced gastric cancer patients with short-term recurrence after postoperative adjuvant therapy, and to identify efficacy-related biomarkers to guide subsequent individualized treatment.

Read the detailed description

The treatment of gastric cancer relies first on surgical resection. Especially for patients with early-stage and locally advanced gastric cancer, surgical resection of the tumor and regional lymph nodes constitutes the most effective therapeutic approach. The goal of surgery is to maximize survival rates and prolong patients' disease-free survival (DFS) by completely eradicating cancer cells . However, due to the high metastatic potential of gastric cancer-particularly lymph node metastasis and peritoneal metastasis-the postoperative recurrence rate remains considerable . Therefore, postoperative adjuvant therapy has become crucial for reducing recurence and improving survival outcomes.

According to the clinical guidelines of the Chinese Society of Clinical Oncology (CSCO) and the European Society for Medical Oncology (ESMO), postoperative adjuvant therapy typically adopts chemotherapy regimens, such as oxaliplatin plus S-1 (SOX), oxaliplatin plus capecitabine (CAPOX), and oxaliplatin plus 5-fluorouracil plus leucovorin (FOLFOX) . These chemotherapy regimens have achieved remarkable results by inhibiting residual micrometastatic tumor cells and reducing the risk of postoperative recurrence.

Nonetheless, despite the certain success of postoperative adjuvant therapy, some patients still experience recurrence either during adjuvant treatment or within 6 months after its completion. Once recurrence occurs, tumor treatment becomes more challenging. Such recurrence usually indicates resistance of the gastric cancer to initial therapy, and the treatment strategy post-recurrence is more complex. For patients with short-term recurrence after postoperative adjuvant therapy, the adjuvant therapy is defined as first-line treatment, and recurrence signifies progression to the second-line treatment phase.The choice of second-line treatment for this specific patient population is generally based on the patients' HER2 expression status. For HER2-positive gastric cancer patients, the trastuzumab plus chemotherapy regimen is usually administered . Multiple clinical trial results have demonstrated that trastuzumab combined with chemotherapy can significantly enhance the efficacy and survival rates of HER2-positive gastric cancer patients . For HER2-negative patients, the RAINBOW study has provided a novel therapeutic regimen of paclitaxel combined with ramucirumab for gastric cancer. The study indicated that the combination of paclitaxel and ramucirumab can significantly prolong patients' median overall survival (OS) and improve their progression-free survival (PFS). This treatment regimen has been recommended by guidelines as the standard second-line treatment option .

In recent years, the emergence of immune checkpoint inhibitors (ICIs)-especially those targeting programmed cell death protein 1 (PD-1) and programmed death-ligand 1 (PD-L1)-has brought revolutionary changes to cancer treatment. Immunotherapy activates the patients' own immune system to recognize and eliminate tumor cells, and it has exhibited significant clinical efficacy in various malignancies, including non-small cell lung cancer, melanoma, and hepatocellular carcinoma . Clinical trials such as ORIENT-16, CheckMate-649, and ATTRACTION-4 have shown that immunotherapy combined with chemotherapy can significantly improve the OS and PFS of patients with PD-L1-positive tumors.The choice of second-line treatment for this specific patient population is generally based on the patients' HER2 expression status. For HER2-positive gastric cancer patients, the trastuzumab plus chemotherapy regimen is usually administered . Multiple clinical trial results have demonstrated that trastuzumab combined with chemotherapy can significantly enhance the efficacy and survival rates of HER2-positive gastric cancer patients . For HER2-negative patients, the RAINBOW study has provided a novel therapeutic regimen of paclitaxel combined with ramucirumab for gastric cancer. The study indicated that the combination of paclitaxel and ramucirumab can significantly prolong patients' median overall survival (OS) and improve their progression-free survival (PFS). This treatment regimen has been recommended by guidelines as the standard second-line treatment option .

In recent years, the emergence of immune checkpoint inhibitors (ICIs)-especially those targeting programmed cell death protein 1 (PD-1) and programmed death-ligand 1 (PD-L1)-has brought revolutionary changes to cancer treatment. Immunotherapy activates the patients' own immune system to recognize and eliminate tumor cells, and it has exhibited significant clinical efficacy in various malignancies, including non-small cell lung cancer, melanoma, and hepatocellular carcinoma . Clinical trials such as ORIENT-16, CheckMate-649, and ATTRACTION-4 have shown that immunotherapy combined with chemotherapy can significantly improve the OS and PFS of patients with PD-L1-positive tumors

Being tested
Sintilimab Combined with Ramucirumab and Paclitaxel
Keywords
gastric cancer
Medical subject headings
Stomach Neoplasms, Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Sintilimab Combined with Ramucirumab and PaclitaxelDrug

    Sintilimab Combined with Ramucirumab and Paclitaxel in the Treatment of Gastric Cancer Patients with Short-term Recurrence after Adjuvant Therapy

Study groups in NCT07669740
Study groupRoleWhat they receive
A Study on the Efficacy and Safety of Sintilimab Combined with Ramucirumab and Paclitaxel in the TreExperimentalA Study on the Efficacy and Safety of Sintilimab Combined with Ramucirumab and Paclitaxel in the Treatment of Gastric Cancer Patients with Short-term Recurrence after Adjuvant Therapy
Receives: Drug: Sintilimab Combined with Ramucirumab and Paclitaxel

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Objective Response Rate (ORR)

    Proportion of patients achieving complete response (CR) or partial response (PR) according to RECIST v1.1.

    Measured: From baseline until disease progression or study completion, assessed up to 24 months

Secondary outcomes (1)
  1. Progression-Free Survival (PFS)

    Progression-free survival is defined as the time from baseline to the first documented disease progression according to RECIST v1.1 or death from any cause, whichever occurs first.

    Measured: From treatment initiation until disease progression or death, whichever occurs first, assessed up to 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Jun 2026
  2. Study start1 Jul 2026 (estimated)
  3. Primary completion1 Jun 2027 (estimated)
  4. Study completion30 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07669740
Sponsor's protocol ID
2025-SR-1145
Status last verified
Jan 2026
First submitted
9 Jan 2026
Last updated
25 Jun 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

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