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

2026年11月8日 更新者: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.

調査の概要

研究の種類

介入

入学 (推定)

680

段階

  • フェーズ2
  • フェーズ 3

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国
        • Beijing Cancer Hospital
    • Shanghai Municipality
      • Shanghai、Shanghai Municipality、中国
        • Zhongshan Hospital, Fudan University

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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

実験的: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

実験的: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

アクティブコンパレータ: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)

実験的: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.

アクティブコンパレータ: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)

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
(phase II)Objective Response Rate assessed by the investigators according to RECIST v1.1
時間枠: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
時間枠: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.

二次結果の測定

結果測定
メジャーの説明
時間枠
(phase II/III)Safety
時間枠:24 months

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

24 months
(phase II/III)OS
時間枠: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
時間枠:24 months
24 months
(phase II/III)The incidence of NAbs
時間枠:24 months
24 months
(phase II/III)Describe the plasma concentrations of total antibodies, binding antibodies, free MMAE and RC148 at each time point.
時間枠:24 months
24 months
(phase III)Progression-Free Survival assessed by the investigators according to RECIST v1.1
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠:24 months
24 months
(phase II/III)Duration of anti-RC118 antibody
時間枠:24 months
24 months
(phase II/III)Titer of anti-RC118 antibody
時間枠:24 months
24 months
(phase II/III)The incidence of anti-RC148 antibody
時間枠:24 months
24 months
(phase II/III)Time to onset of anti-RC148 antibody
時間枠:24 months
24 months
(phase II/III)Duration of anti-RC148 antibody
時間枠:24 months
24 months
(phase II/III)Titer of anti-RC148 antibody
時間枠:24 months
24 months
(phase II/III)Area under the plasma concentration-time curve (AUC) of RC118 binding antibodies, free MMAE and RC148.
時間枠: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.
時間枠: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.
時間枠: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
時間枠:24 months
24 months
Change From Baseline in Gastric Cancer Symptom Scores Assessed by EORTC QLQ-STO22
時間枠:24 months
24 months
Change From Baseline in EQ-5D-5L Health Utility Index Score
時間枠:24 months
24 months
Change From Baseline in EQ-5D Visual Analogue Scale (EQ-VAS) Score
時間枠:24 months
24 months

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年11月1日

一次修了 (推定)

2030年4月30日

研究の完了 (推定)

2031年12月31日

試験登録日

最初に提出

2026年11月1日

QC基準を満たした最初の提出物

2026年11月8日

最初の投稿 (実際)

2026年11月13日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月13日

QC基準を満たした最後の更新が送信されました

2026年11月8日

最終確認日

2026年10月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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