Ta strona została przetłumaczona automatycznie i dokładność tłumaczenia nie jest gwarantowana. Proszę odnieść się do angielska wersja za tekst źródłowy.

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

8 listopada 2026 zaktualizowane przez: 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.

Przegląd badań

Status

Jeszcze nie rekrutacja

Warunki

Interwencja / Leczenie

Typ studiów

Interwencyjne

Zapisy (Szacowany)

680

Faza

  • Faza 2
  • Faza 3

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

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

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat i starsze (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Opis

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.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: 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

Eksperymentalny: 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

Eksperymentalny: 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

Aktywny komparator: 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)

Eksperymentalny: 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.

Aktywny komparator: 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)

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Ramy czasowe
(phase II)Objective Response Rate assessed by the investigators according to RECIST v1.1
Ramy czasowe: 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
Ramy czasowe: 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.

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
(phase II/III)Safety
Ramy czasowe: 24 months

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

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

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 listopada 2026

Zakończenie podstawowe (Szacowany)

30 kwietnia 2030

Ukończenie studiów (Szacowany)

31 grudnia 2031

Daty rejestracji na studia

Pierwszy przesłany

1 listopada 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

8 listopada 2026

Pierwszy wysłany (Rzeczywisty)

13 listopada 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

13 listopada 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

8 listopada 2026

Ostatnia weryfikacja

1 października 2026

Więcej informacji

Terminy związane z tym badaniem

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .