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

8. november 2026 oppdatert av: 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.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

680

Fase

  • Fase 2
  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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

Eksperimentell: 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

Eksperimentell: 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

Aktiv 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)

Eksperimentell: 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.

Aktiv 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)

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
(phase II)Objective Response Rate assessed by the investigators according to RECIST v1.1
Tidsramme: 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
Tidsramme: 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.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
(phase II/III)Safety
Tidsramme: 24 months

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

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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. november 2026

Primær fullføring (Antatt)

30. april 2030

Studiet fullført (Antatt)

31. desember 2031

Datoer for studieregistrering

Først innsendt

1. november 2026

Først innsendt som oppfylte QC-kriteriene

8. november 2026

Først lagt ut (Faktiske)

13. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

13. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

8. november 2026

Sist bekreftet

1. oktober 2026

Mer informasjon

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