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RC118 Combined With RC148 as First-Line Treatment for Claudin 18.2-Positive, HER2-Negative Advanced G/GEJ Adenocarcinoma

2026년 11월 8일 업데이트: RemeGen Co., Ltd.

A Randomized, Controlled, Open-Label, Multicenter Phase II/III Study to Evaluate the Efficacy and Safety of RC118 in Combination With RC148 Versus PD-1 Inhibitor Plus Chemotherapy as First-Line Treatment for Claudin 18.2-Positive, HER2-Negative Locally Advanced Unresectable or Metastatic Gastric/Gastroesophageal Junction Adenocarcinoma

This is a randomized, controlled, open-label, multicenter Phase II/III study evaluating the efficacy and safety of RC118 (an antibody-drug conjugate targeting Claudin 18.2) in combination with RC148 versus PD-1 inhibitor (Tislelizumab) plus chemotherapy (CAPOX) as first-line treatment in patients with Claudin 18.2-positive and HER2-negative locally advanced unresectable or metastatic gastric or gastroesophageal junction (G/GEJ) adenocarcinoma.

The study consists of two phases: Phase II will explore the optimal dose combination of RC118 and RC148 across three experimental arms versus a standard comparator arm. Phase III will evaluate the efficacy (progression-free survival) of the recommended Phase III dose (RP3D) combination versus standard of care.

연구 개요

상태

아직 모집하지 않음

정황

개입 / 치료

연구 유형

중재적

등록 (추정된)

680

단계

  • 2 단계
  • 3단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Beijing Municipality
      • Beijing, Beijing Municipality, 중국
        • Beijing Cancer Hospital
    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, 중국
        • Zhongshan Hospital, Fudan University

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  1. Voluntarily consent to participate and sign the informed consent form.
  2. Age ≥ 18 years.
  3. Expected survival > 12 weeks.
  4. ECOG performance status of 0 or 1.
  5. Histologically confirmed unresectable locally advanced or metastatic gastric/gastroesophageal junction adenocarcinoma.
  6. No prior systemic antitumor therapy for locally advanced or metastatic gastric cancer. If neoadjuvant or adjuvant therapy has been received, disease recurrence or metastasis must occur ≥ 6 months after the end of such therapy.
  7. The participant agrees to provide adequate fresh tumor tissue samples or archival paraffin tissue samples collected within the previous 3 years for Claudin 18.2 expression testing. The Claudin 18.2 test result from the central laboratory shows positive Claudin 18.2 expression.
  8. Have a local laboratory report confirming HER2 negativity; have a qualified PD-L1 expression test result from a local laboratory or central laboratory.
  9. Have at least one measurable lesion per RECIST v1.1.
  10. Adequate bone marrow, hepatic and renal function.
  11. Male and female participants of reproductive potential must use medically acceptable contraceptive measures from the signing of informed consent until 12 months after the last study treatment. Female participants of reproductive potential must have a negative serum pregnancy test within 7 days before the first dose of study treatment, and agree not to breastfeed or donate oocytes from signing informed consent until 12 months after the last study treatment. Male participants must agree not to donate sperm from signing informed consent until 12 months after the last study treatment.
  12. Able to understand the study requirements, and be willing and able to comply with study and follow-up procedures.

Exclusion Criteria:

  1. Prior receipt of any antibody drug conjugate, Claudin 18.2 targeted therapy, or concurrent antitumor therapy targeting vascular endothelial growth factor / vascular endothelial growth factor receptor and PD 1/PD L1.
  2. Received palliative therapy for localized lesions within 2 weeks prior to randomization, or radiotherapy to the primary gastric lesion within 4 weeks prior to randomization.
  3. Received traditional Chinese medicines with antitumor indications, or chemical drugs or biological products with immunomodulatory effects within 2 weeks prior to randomization.
  4. Participated in another drug clinical trial and received investigational product within 4 weeks prior to randomization.
  5. Underwent major surgery or tumor interventional therapy within 4 weeks prior to randomization, with incomplete recovery, or major surgery anticipated during study treatment.
  6. Received live vaccines within 4 weeks prior to randomization or planned to receive any live vaccine during the study.
  7. Systemic treatment with corticosteroids or other immunosuppressive agents, either ongoing use or requiring chronic use, within 2 weeks prior to randomization.
  8. Presence of leptomeningeal metastasis, spinal cord compression or brainstem metastasis; symptomatic brain metastasis; untreated brain metastasis; symptomatic treatment such as corticosteroids for brain metastasis within 4 weeks prior to randomization; radiotherapy and/or surgery for brain metastasis within 4 weeks prior to randomization; progression of brain metastasis during or after local therapy.
  9. Bone metastases with risk of paraplegia.
  10. Per CTCAE Version 6.0: peripheral neuropathy ≥ Grade 2; residual toxicity from prior antitumor therapy ≥ Grade 2.
  11. Clinically significant bleeding events or bleeding diathesis within 2 months prior to randomization.
  12. Severe gastrointestinal dysfunction that may affect drug intake, transit or absorption; significant malnutrition.
  13. History of gastrointestinal perforation or fistula, bowel obstruction, inflammatory bowel disease or bowel resection within 6 months prior to randomization.
  14. Clinically symptomatic third space effusion requiring intervention within 2 weeks prior to randomization.
  15. Active autoimmune disease requiring systemic therapy within 2 years prior to randomization.
  16. History of other acquired or congenital immunodeficiency disorders, allogeneic hematopoietic stem cell transplantation or solid organ transplantation.
  17. Active or uncontrolled infection within 2 weeks prior to randomization.
  18. Severe or inadequately controlled systemic disease.
  19. Diagnosis of interstitial lung disease (ILD); or moderate or worse impairment of pulmonary function.
  20. History of active or severe cardiac disease.
  21. Severe arterial/venous thromboembolic events, or cerebrovascular accidents within 6 months prior to randomization.
  22. History of severe coagulopathy, and receiving anticoagulants for therapeutic purposes (prophylactic anticoagulation is excluded).
  23. Concurrent second primary malignancy.
  24. Hypersensitivity or intolerance to known components of the investigational product or analogous agents.
  25. Active infectious disease.
  26. Known dihydropyrimidine dehydrogenase (DPD) deficiency.
  27. Pregnant or lactating women.
  28. Any other disease, metabolic abnormality, abnormal physical finding or laboratory abnormality that raises suspicion of a condition rendering the participant unsuitable for the investigational product, that would confound the interpretation of study results, or that places the participant at substantial risk.
  29. Psychiatric disorder, history of substance abuse or social circumstances that may compromise study compliance. Participants judged to have inadequate adherence to this clinical trial, or with other factors making participation inappropriate.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: RC118(Dose 1) plus RC148(Dose 1)

RC118 and RC148 each have 2 dose levels. This study is designed with 3 arms to screen and confirm the dose.

Dose1+Dose1

실험적: RC118(Dose 1) plus RC148(Dose 2)

RC118 and RC148 each have 2 dose levels. This study is designed with 3 arms to screen and confirm the dose.

Dose1+Dose2

실험적: RC118(Dose 2) plus RC148(Dose 1)

C118 and RC148 each have 2 dose levels. This study is designed with 3 arms to screen and confirm the dose.

Dose2+Dose1

활성 비교기: Tislelizumab+ Oxaliplatin + Capecitabine

Tislelizumab (200 mg Q3W) + Oxaliplatin (130 mg/m² Q3W, max 6 cycles) + Capecitabine (1000 mg/m² BID, D1-14 Q3W)

Tislelizumab (200 mg Q3W) + Oxaliplatin (130 mg/m² Q3W, max 6 cycles) + Capecitabine (1000 mg/m² BID, D1-14 Q3W)

실험적: RC118 plus RC148(phase III)

The dose for Phase III will be determined based on Phase II results.

The dose for Phase III will be determined based on Phase II results.

활성 비교기: Tislelizumab + Oxaliplatin + Capecitabine (phase III)

Tislelizumab (200 mg Q3W) + Oxaliplatin (130 mg/m² Q3W, max 6 cycles) + Capecitabine (1000 mg/m² BID, D1-14 Q3W)

Tislelizumab (200 mg Q3W) + Oxaliplatin (130 mg/m² Q3W, max 6 cycles) + Capecitabine (1000 mg/m² BID, D1-14 Q3W)

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
(phase II)Objective Response Rate assessed by the investigators according to RECIST v1.1
기간: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.
From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.
(phase III)Progression-Free Survival assessed by the BIRC according to RECIST v1.1
기간: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.
From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.

2차 결과 측정

결과 측정
측정값 설명
기간
(phase II/III)Safety
기간: 24 months

Safety and tolerability as evaluated in terms of incidence of AEs and SAEs

24 months
(phase II/III)OS
기간: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.
From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.
(phase II/III)The incidence of anti-RC118 antibody
기간: 24 months
24 months
(phase II/III)The incidence of NAbs
기간: 24 months
24 months
(phase II/III)Describe the plasma concentrations of total antibodies, binding antibodies, free MMAE and RC148 at each time point.
기간: 24 months
24 months
(phase III)Progression-Free Survival assessed by the investigators according to RECIST v1.1
기간: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.
From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.
(phase III)ORR assessed by BIRC and investigators per RECIST v1.1
기간: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
(phase III)DCR assessed by BIRC and investigators per RECIST v1.1
기간: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
(phase III)DoR assessed by BIRC and investigators per RECIST v1.1
기간: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
(phase II)DoR assessed by investigators per RECIST v1.1
기간: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
(phase II)DCR assessed by investigators per RECIST v1.1
기간: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
(phase II)PFS assessed by investigators per RECIST v1.1
기간: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months
(phase II/III)Time to onset of anti-RC118 antibody
기간: 24 months
24 months
(phase II/III)Duration of anti-RC118 antibody
기간: 24 months
24 months
(phase II/III)Titer of anti-RC118 antibody
기간: 24 months
24 months
(phase II/III)The incidence of anti-RC148 antibody
기간: 24 months
24 months
(phase II/III)Time to onset of anti-RC148 antibody
기간: 24 months
24 months
(phase II/III)Duration of anti-RC148 antibody
기간: 24 months
24 months
(phase II/III)Titer of anti-RC148 antibody
기간: 24 months
24 months
(phase II/III)Area under the plasma concentration-time curve (AUC) of RC118 binding antibodies, free MMAE and RC148.
기간: 24 months

AUC derived via population pharmacokinetic (PopPK) analysis, if data permit.

24 months
(phase II/III)Time to maximum plasma concentration (Tmax) of RC118 binding antibodies, free MMAE and RC148.
기간: 24 months

Tmax derived via population pharmacokinetic (PopPK) analysis, if data permit.

24 months
(phase II/III)Maximum observed plasma concentration (Cmax) of RC118 binding antibodies, free MMAE and RC148.
기간: 24 months

Cmax derived via population pharmacokinetic (PopPK) analysis, if data permit.

24 months
Change From Baseline in Global Health Status/Quality of Life (GHS/QoL) Score Assessed by EORTC QLQ-C30
기간: 24 months
24 months
Change From Baseline in Gastric Cancer Symptom Scores Assessed by EORTC QLQ-STO22
기간: 24 months
24 months
Change From Baseline in EQ-5D-5L Health Utility Index Score
기간: 24 months
24 months
Change From Baseline in EQ-5D Visual Analogue Scale (EQ-VAS) Score
기간: 24 months
24 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 11월 1일

기본 완료 (추정된)

2030년 4월 30일

연구 완료 (추정된)

2031년 12월 31일

연구 등록 날짜

최초 제출

2026년 11월 1일

QC 기준을 충족하는 최초 제출

2026년 11월 8일

처음 게시됨 (실제)

2026년 11월 13일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 11월 13일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 11월 8일

마지막으로 확인됨

2026년 10월 1일

추가 정보

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약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

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미국 FDA 규제 기기 제품 연구

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