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NCT Number: NCT06944496

A Study of Disitamab Vedotin Combined With Tislelizumab and Chemotherapy Versus Tislelizumab Combined With Chemotherapy in HER2-Low Advanced Gastric or Gastroesophageal Junction Adenocarcinoma

The purpose of this study is to evaluate the efficacy and safety of **Disitamab Vedotin combined with Tislelizumab and CAPOX versus Tislelizumab combined with CAPOX** as first-line treatment for patients with HER2-low advanced gastric or gastroesophageal junction adenocarcinoma.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Beijing Cancer Hospital

Beijing, BJ-Beijing, 100021, China

Location contact

shen lin shen, PhD

CONTACT

18018029623

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Voluntarily consent to participate in the study and sign the informed consent form
  • Expected survival period >12 weeks
  • ECOG Performance Status 0 or 1
  • Histologically confirmed unresectable locally advanced, metastatic, or recurrent gastric or gastroesophageal junction adenocarcinoma
  • No prior systemic therapy for locally advanced or metastatic gastric cancer
  • HER2-low expression
  • At least one assessable lesion according to RECIST v1.1 criteria
  • Adequate organ function
  • For female subjects: They should be surgically sterilized, postmenopausal, or agree to use a medically approved contraceptive method (such as an intrauterine device, contraceptive pill, or condom) during the study treatment period and for 6 months after the end of the study treatment. A blood pregnancy test must be negative within 7 days before the study medication is administered, and they must not be breastfeeding
  • For male subjects: They should be surgically sterilized or agree to use a medically approved contraceptive method during the study treatment period and for 6 months after the end of the study treatment
  • Able to understand the study requirements and willing to comply with the study and follow-up procedures

Exclusion criteria

  • Presence of central nervous system (CNS) metastasis and/or carcinomatous meningitis
  • Peripheral neuropathy > Grade 1
  • Tumor lesions with a tendency to bleed
  • Uncontrolled diarrhea
  • Bone metastases with a risk of paraplegia
  • Past or current interstitial lung disease, or presence of drug-induced pneumonia, radiation pneumonia, or severely impaired lung function
  • Other malignancies within 5 years before the first dose, except for those expected to be cured with treatment (e.g., adequately treated thyroid cancer, cervical carcinoma in situ, basal or squamous cell skin cancer, or ductal carcinoma in situ of the breast treated with curative surgery)
  • Pregnant or breastfeeding women

Treatment and study plan

Disitamab Vedotin+Tislelizumab+Oxaliplatin+Capecitabine

Biological

Disitamab Vedotin: 2.5 mg/kg, IV, D1, Q2W; Tislelizumab: 200 mg, IV, D1, Q3W Oxaliplatin: 100 mg/m², IV, D1, Q3W; Capecitabine: 750 mg/m², po, BID, D1-D14, Q3W

Tislelizumab+Oxaliplatin+Capecitabine

Biological

Tislelizumab: 200 mg, IV, D1, Q3W Oxaliplatin: 130 mg/m², IV, D1, Q3W; Capecitabine: 1000 mg/m², po, BID, D1-D14, Q3W

Primary outcomes

  1. Progression-Free Survival

    Time frame: 24 months

Secondary outcomes

  1. Overall Survival

    Time frame: up to 5 years

  2. Objective Response Rate

    Time frame: 24 months

  3. Disease Control Rate

    Time frame: 24 months

  4. Duration of Response

    Time frame: 24 months

  5. Patient-Reported Outcomes

    Time frame: 24 months

  6. Adverse Events

    Time frame: 24 months

Study contacts

Contact information is provided by the study sponsor or research team.

SU Xiaohong Study Director, M.D

CONTACT

[email protected]

+0810-65391479

Sponsors and collaborators

Lead sponsor

RemeGen Co., Ltd.

Industry

Registry information

Official study title

A Phase III, Randomized Trial Comparing RC48 Plus Chemotherapy and Tislelizumab With Tislelizumab Plus Chemotherapy as First-line Treatment in Participants With HER2 Low Advanced Gastric or Gastrioesophageal Junction Adenocarcinoma (RC48-C039)

Important dates

Study start
2025
Primary completion
2028
Study completion
2030
First posted
Apr 25, 2025
Registry last updated
Apr 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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