Evaluating a new treatment for advanced gastric cancer

A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of Disitamab Vedotin Combined With RC98 in the Treatment of Subjects With HER2-expressing Locally Advanced or Metastatic Gastric Cancer (Including AEG).

This study is testing a new combination treatment for people with advanced gastric cancer who haven't had success with standard therapies to see if it can help them feel better.

Quick facts

• Phase: Phase 1
• Study type: Interventional
• Enrollment: 24 (estimated)
• Ages: 18 Years to 70 Years
• Sex: All
• Sponsor: RemeGen Co., Ltd. (Industry-sponsored)
• Drugs / interventions: chemotherapy, radiation, prednisone
• Locations: 1 site (Beijing, Beijing)
• Trial ID: NCT05514158 on ClinicalTrials.gov

What this trial studies

This clinical trial is a single-center, open-label, dose-escalation phase I study aimed at assessing the safety, tolerability, pharmacokinetics, and preliminary efficacy of a combination therapy involving Disitamab Vedotin (RC48-ADC) and RC98 in patients with HER2-expressing locally advanced or metastatic gastric cancer. The study will enroll subjects who have experienced disease progression after standard treatments or are intolerant to them. Participants will receive escalating doses of RC98 alongside a fixed dose of RC48-ADC, with careful monitoring for dose-limiting toxicities and overall treatment response.

Who should consider this trial

Good fit: Ideal candidates for this study are adults aged 18-70 with HER2-expressing locally advanced or metastatic gastric cancer who have progressed after standard treatment.

Not a fit: Patients with early-stage gastric cancer or those who have not yet undergone standard treatment may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could provide a new therapeutic option for patients with advanced gastric cancer who have limited treatment alternatives.

How similar studies have performed: While this approach is novel in its specific combination, similar studies involving HER2-targeted therapies have shown promise in treating gastric cancer.

Eligibility criteria

Inclusion Criteria:

1. Voluntarily agree to participate in the research and sign the informed consent;
2. Age 18-70 (including 18 and 70);
3. Expected survival period ≥ 12 weeks;
4. ECOG performance status of 0 or 1 within 3 days before the first dose of study treatment;
5. Patients with metastatic or unresectable locally advanced or metastatic gastric cancer (including gastroesophageal junction adenocarcinoma) confirmed by histology or cytology with disease progression after standard treatment or intolerant to standard treatment;
6. Female subjects should be surgically sterilized, postmenopausal patients, or agree to use at least one medically approved contraceptive measure (such as an intrauterine device, contraceptives) during the study treatment period and within 6 months after the end of the study treatment period. pills or condoms), must have a negative blood pregnancy test within 7 days prior to study enrollment, and must be non-nursing. Male subjects should agree to use at least one medically approved contraceptive method during the study treatment period and within 6 months after the end of the study treatment period;
7. Able to understand trial requirements, willing and able to comply with trial and follow-up procedures.

Adequate organ and bone marrow hematopoiesis 8. Bone marrow function:

* Hemoglobin≥90g/L;
* Absolute neutrophil count ≥1.5×109/L;
* Platelets≥100 × 109/L; 9. Liver function (subject to the normal value of the clinical trial center):
* In the absence of liver metastases, the total serum bilirubin is ≤1.5 times the ULN; in the presence of liver metastases, the total serum bilirubin is ≤3 times the ULN;
* In the absence of liver metastases, both ALT and AST are ≤3 times ULN, and in the presence of liver metastases, both ALT and AST are ≤5 times ULN; 10. Renal function (subject to the normal value of the clinical trial center):
* Serum creatinine ≤ 1.5 times ULN, or creatinine clearance (CrCl) ≥ 60 mL/min calculated by the Cockcroft-Gault formula, or 24-hour urine CrCl ≥ 60 mL/min; 11. Coagulation function: International normalized ratio (INR), activated partial thromboplastin time (APTT) and prothrombin time (PT) are all ≤1.5 times ULN; 12. Endocrine function: Thyroid-stimulating hormone (TSH) or free thyroxine (FT4) or free triiodothyronine (FT3) are within the normal range of ±10%; 13. Heart function:
* New York Heart Association (NYHA) class \<3;
* Left ventricular ejection fraction ≥50%; 14. At least one measurable lesion according to RECIST 1.1 criteria; 15. The HER2 IHC test results are IHC 1+, IHC 2+ or IHC 3+, the subject's previous test results (confirmed by the investigator) or the test results of the research center are acceptable, and can provide a diagnosis of locally advanced or metastatic gastric cancer of tumor tissue specimens, as well as a sufficient number of paraffin blocks, tissue sections (5-10 unstained) for biomarker detection.

Exclusion Criteria:

1. The study drug has been used within 4 weeks before the start of the study drug;
2. Major surgery has been performed within 4 weeks before the start of the study drug and the patient has not fully recovered;
3. Have been vaccinated with live vaccines within 4 weeks before the start of the study drug or plan to receive any vaccines during the study period (except for the new coronavirus vaccine);
4. Arterial/venous thrombotic events, such as cerebrovascular accident (including temporary ischemic attack), deep vein thrombosis and pulmonary embolism, occurred within 6 months before the study drug;
5. Major cardiovascular disease (NYHA grade 3 or 4 heart failure, second-degree or higher heart block, myocardial infarction within the past 12 months, unstable arrhythmia or unstable angina pectoris, cerebral infarction within 6 months infarction, etc.);
6. Active autoimmune disease requiring systemic treatment (such as the use of immunomodulatory drugs, corticosteroids or immunosuppressants) within 2 years before the start of study administration, allowing related replacement therapy (such as thyroxine, insulin, or renal or Physiological corticosteroid replacement therapy for pituitary insufficiency);
7. Subjects who need to receive glucocorticoid (prednisone\>10 mg/day or other similar drugs at an equivalent dose) or other immunosuppressive therapy due to certain conditions within 14 days before the start of the study drug;
8. Suffering from uncontrolled systemic diseases, including diabetes, hypertension, pulmonary fibrosis, acute lung disease, interstitial lung disease, liver cirrhosis, etc.;
9. Suffering from active infection requiring systemic treatment;
10. History of active tuberculosis;
11. Positive human immunodeficiency virus (HIV) test result;
12. Hepatitis B surface antigen (HBsAg) positive and HBV DNA copy number greater than the upper limit of the normal value of the laboratory department of the research center; or hepatitis C virus (HCV) antibody positive and the HCV RNA copy number greater than the upper limit of the normal value of the laboratory department of the research center;
13. Conditions that the investigator believes will affect the safety or compliance of the drug treatment in this study, including but not limited to moderate to large amounts of pleural/ascites/pericardial effusion, difficult-to-correct pleural/ascites/pericardial effusion, mental illness, etc.;
14. Known to have hypersensitivity reactions or delayed allergic reactions to certain components of RC98 for injection or similar drugs;
15. Those who are known to be allergic to recombinant humanized anti-HER2 monoclonal antibody-MMAE conjugate drugs and their components;
16. Previously received PD-(L)1 inhibitor or other antibody-conjugated drug therapy;
17. Suffering from any other disease, metabolic abnormality, abnormal physical examination or abnormal laboratory test, according to the judgment of the investigator, there is reason to suspect that the subject has a certain disease or condition that is not suitable for the use of the study drug, or will affect the research results interpretations, or situations that place the subject at high risk;
18. Women who are pregnant or breastfeeding or women/men who are planning to give birth;
19. It is estimated that the subjects' compliance to participate in this clinical study is insufficient or the investigators believe that there are other factors that are not suitable for participating in this study; tumor related
20. Suffering from central nervous system metastases and/or cancerous meningitis. Subjects who have previously received treatment for brain metastases may be considered for participation in this study, provided that their disease has been stable for at least 3 months, no disease progression has been confirmed by imaging within 4 weeks prior to the first dose of the study, and all neurological symptoms have recovered At baseline, there was no evidence of new or enlarging brain metastases, and radiation, surgery, or steroid therapy was discontinued at least 28 days prior to the first dose of study treatment. This exception does not include cancerous meningitis, which should be excluded regardless of its clinically stable status;
21. Suffering from other malignant tumors within 5 years before signing the informed consent form (non-melanoma skin cancer, cervical carcinoma in situ or other tumors that have been effectively treated, except for malignant tumors that are considered cured);
22. Received chemotherapy and radiotherapy within 4 weeks before the start of the study drug;
23. Subjects who have received immune-enhancing therapy (such as alpha-interferon, interleukin-2) within 2 weeks before the start of the study drug.
24. Received hormone therapy for the tumor within 2 weeks before the start of the study drug;
25. Received palliative radiotherapy for bone metastases within 2 weeks before the start of the study drug;
26. Received anti-tumor traditional Chinese medicine treatment within 2 weeks before the start of the study drug;
27. The toxicity caused by previous anti-tumor therapy has not recovered to CTCAE (version 5.0) grade 0-1 (except for 2nd degree alopecia);

Where this trial is running

Beijing, Beijing

• Remegen — Beijing, Beijing, China (Recruiting)

Study contacts

• Principal investigator: yi Ba, ph.D — Tianjin Cancer Hospital
• Study coordinator: Jianming Fang, ph.D

Conditions Gastric Cancer