ClinicalTrials.gg
Not yet recruitingNCT07935369Updated Nov 13, 2026

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

A Phase 2/3 interventional study of RC118(Dose 1) plus RC148(Dose 1) and RC118(Dose 1) plus RC148(Dose 2) in Advanced Gastric or Gastroesophageal Junction Adenocarcinoma, sponsored by RemeGen Co., Ltd.. Not yet recruiting at 2 sites in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-13.

Sponsored by RemeGen Co., Ltd. · Phase 2/3, Interventional, and Treatment

Updated Nov 13, 2026Newly registeredGo to Updates ↓

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Phase
Phase 2/3
Study type
Interventional
Enrollment
680
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Advanced Gastric or Gastroesophageal Junction Adenocarcinoma
03

In context

Lead sponsor

RemeGen Co., Ltd. is the lead sponsor of 83 studies on the registry; 42 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Voluntarily consent to participate and sign the form.
  2. Age ≥ 18 years.
  3. Expected survival > 12 weeks.
  4. performance status of 0 or 1.
  5. confirmed unresectable locally advanced or gastric/gastroesophageal junction adenocarcinoma.
  6. No prior systemic antitumor therapy for locally advanced or metastatic gastric cancer. If 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 negativity; have a qualified expression test result from a local laboratory or central laboratory.
  9. Have at least one per v1.1.
  10. Adequate bone marrow, hepatic and renal function.
  11. Male and female participants of must use medically acceptable 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

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 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 within 4 weeks prior to randomization or planned to receive any live vaccine during the study.
  7. Systemic treatment with or other agents, either ongoing use or requiring chronic use, within 2 weeks prior to randomization.
  8. Presence of , spinal cord compression or brainstem ; symptomatic ; 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 Version 6.0: peripheral neuropathy ≥ Grade 2; residual toxicity from prior antitumor therapy ≥ Grade 2.
  11. 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 disease requiring systemic therapy within 2 years prior to randomization.
  16. History of other acquired or congenital immunodeficiency disorders, 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 .
  24. 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.
Terms in these criteria, in plain language(23)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

Adjuvant and neoadjuvant

Neoadjuvant treatment is given before the main treatment (usually surgery), often to shrink a tumour. Adjuvant treatment is given after it, to lower the chance of the cancer coming back.

HER2

HER2 is a protein, made from the ERBB2 gene, that drives the growth of some cancers. A study may look for a level of the protein, extra copies of the gene, or a particular change in it.

In breast cancer, protein tests are read as HER2-positive, HER2-low or HER2-negative; other cancers use their own rules. Check which test result the study requires.

PD-1, PD-L1 and checkpoint inhibitors

PD-1, PD-L1 and CTLA-4 are proteins that act as brakes on the immune system. Checkpoint inhibitors, such as pembrolizumab or nivolumab, block them so the immune system can attack a cancer.

PD-L1 can also be measured in a tumour sample. Some scores count stained tumour cells only (TPS); others also count certain immune cells (CPS). The study names the score and the minimum it uses.

Measurable disease

The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.

The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.

RECIST

The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.

“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.

Reproductive potential

Able to have children. For women this usually means from the first period until menopause, unless permanently unable to through surgery; for men, unless permanently sterile. Read who the line is about — participants, women, men, or their partners.

Criteria about it usually ask for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Live vaccines

Vaccines made with a weakened form of the germ, such as measles–mumps–rubella (MMR), chickenpox and yellow fever. They can be risky when the immune system is weakened. Flu injections are not live; the nasal flu spray is.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Leptomeningeal disease

Cancer that has spread to the leptomeninges, the thin layers covering the brain and spinal cord, and the fluid between them. It is not the same as brain metastases.

Criteria often treat it separately, and many studies leave it out even where treated brain metastases are allowed.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

Studies differ: some leave out any brain metastases, some accept ones treated and stable for some weeks. Check what this study allows.

CTCAE grade

The US National Cancer Institute’s scale of how severe an adverse event is — any unwanted medical event during a study, such as a symptom, an illness or an abnormal test result, whether or not a treatment caused it. Whether it did is judged separately.

1
Mild.
2
Moderate.
3
Severe.
4
Life-threatening.
5
Death due to the event.

“Side effects of earlier treatment resolved to grade 1 or less” means they have settled to mild or gone.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Allogeneic and autologous transplant

Stem cell (bone marrow) transplants. Allogeneic uses cells from a donor; autologous uses your own cells, collected earlier and given back.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
680 participants (estimated)

Study arms

  • Experimental
    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.

    Drug: RC118(Dose 1) plus RC148(Dose 1)

  • Experimental
    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.

    Drug: RC118(Dose 1) plus RC148(Dose 2)

  • Experimental
    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.

    Drug: RC118(Dose 2) plus RC148(Dose 1)

  • Active comparator
    Tislelizumab+ Oxaliplatin + Capecitabine

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

    Drug: Tislelizumab Injection plus Oxaliplatin for Injection plus Capecitabine Tablets

  • Experimental
    RC118 plus RC148(phase III)

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

    Drug: RC118 plus RC148 (phase III)

  • Active comparator
    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)

    Drug: Tislelizumab Injection plus Oxaliplatin for Injection plus Capecitabine Tablets (phase III)(phase III)

Interventions

  • DrugRC118(Dose 1) plus RC148(Dose 1)

    Dose1+Dose1

  • DrugRC118(Dose 1) plus RC148(Dose 2)

    Dose1+Dose2

  • DrugRC118(Dose 2) plus RC148(Dose 1)

    Dose2+Dose1

  • DrugTislelizumab Injection plus Oxaliplatin for Injection plus Capecitabine Tablets

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

  • DrugRC118 plus RC148 (phase III)

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

  • DrugTislelizumab Injection plus Oxaliplatin for Injection plus Capecitabine Tablets (phase III)(phase III)

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

06

What researchers measure

Primary outcomes

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

    Time frame: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.

  2. (phase III)Progression-Free Survival assessed by the BIRC according to RECIST v1.1

    Time frame: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.

Secondary outcomes

  1. (phase II/III)Safety

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

    Time frame: 24 months

  2. (phase II/III)OS

    Time frame: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.

  3. (phase II/III)The incidence of anti-RC118 antibody

    Time frame: 24 months

  4. (phase II/III)The incidence of NAbs

    Time frame: 24 months

  5. (phase II/III)Describe the plasma concentrations of total antibodies, binding antibodies, free MMAE and RC148 at each time point.

    Time frame: 24 months

  6. (phase III)Progression-Free Survival assessed by the investigators according to RECIST v1.1

    Time frame: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months.

  7. (phase III)ORR assessed by BIRC and investigators per RECIST v1.1

    Time frame: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months

  8. (phase III)DCR assessed by BIRC and investigators per RECIST v1.1

    Time frame: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months

  9. (phase III)DoR assessed by BIRC and investigators per RECIST v1.1

    Time frame: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months

  10. (phase II)DoR assessed by investigators per RECIST v1.1

    Time frame: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months

  11. (phase II)DCR assessed by investigators per RECIST v1.1

    Time frame: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months

  12. (phase II)PFS assessed by investigators per RECIST v1.1

    Time frame: From randomization date until disease progression, lost to follow-up, withdrawal of informed consent or death, assessed up to approximately 24 months

  13. (phase II/III)Time to onset of anti-RC118 antibody

    Time frame: 24 months

  14. (phase II/III)Duration of anti-RC118 antibody

    Time frame: 24 months

  15. (phase II/III)Titer of anti-RC118 antibody

    Time frame: 24 months

  16. (phase II/III)The incidence of anti-RC148 antibody

    Time frame: 24 months

  17. (phase II/III)Time to onset of anti-RC148 antibody

    Time frame: 24 months

  18. (phase II/III)Duration of anti-RC148 antibody

    Time frame: 24 months

  19. (phase II/III)Titer of anti-RC148 antibody

    Time frame: 24 months

  20. (phase II/III)Area under the plasma concentration-time curve (AUC) of RC118 binding antibodies, free MMAE and RC148.

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

    Time frame: 24 months

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

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

    Time frame: 24 months

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

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

    Time frame: 24 months

  23. Change From Baseline in Global Health Status/Quality of Life (GHS/QoL) Score Assessed by EORTC QLQ-C30

    Time frame: 24 months

  24. Change From Baseline in Gastric Cancer Symptom Scores Assessed by EORTC QLQ-STO22

    Time frame: 24 months

  25. Change From Baseline in EQ-5D-5L Health Utility Index Score

    Time frame: 24 months

  26. Change From Baseline in EQ-5D Visual Analogue Scale (EQ-VAS) Score

    Time frame: 24 months

07

Study locations

2 sites
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Nov 2026; primary completion for Apr 2030, 41 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 1, 2026
First posted
Nov 13, 2026
StartEst.
Nov 2026
Primary completionEst.
Apr 30, 2030
CompletionEst.
Dec 31, 2031
Last update
Nov 13, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 13, 2026
Show all 1 update
  1. Nov 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07935369
Lead sponsor
RemeGen Co., Ltd.
Responsible party
Sponsor
First posted
Nov 13, 2026
Start date
Nov 2026 (estimated)
Primary completion
Apr 30, 2030 (estimated)
Completion
Dec 31, 2031 (estimated)
Last update
Nov 13, 2026

Study contacts

Hongfang Li
Contact
Hongfang.li@remegen.com
010-65384976

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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