Combination of VG161 and Nivolumab for Advanced Metastatic Gastric Cancer

A Dose Ascending, Open Phase Ib/IIa Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics and Preliminary Efficacy of VG161 Combined With Nivolumab Injection in Subjects With Metastatic Gastric Cancer

This study is testing a new combination of two treatments for people with advanced stomach cancer to see if it is safe and effective after they have already tried other therapies.

Quick facts

• Phase: Phase1; Phase2
• Study type: Interventional
• Enrollment: 43 (estimated)
• Ages: 18 Years to 75 Years
• Sex: All
• Sponsor: CNBG-Virogin Biotech (Shanghai) Ltd. (Industry-sponsored)
• Drugs / interventions: nivolumab, chemotherapy, immunotherapy, prednisone
• Locations: 1 site (Beijing, Beijing Municipality)
• Trial ID: NCT06008925 on ClinicalTrials.gov

What this trial studies

This clinical trial evaluates the safety and efficacy of VG161, a recombinant human-IL12/15/PDL1B oncolytic HSV-1 injection, combined with nivolumab in patients with advanced metastatic gastric or gastroesophageal junction adenocarcinoma. The study is divided into two parts: the first part focuses on determining the recommended safe dose and assessing safety, while the second part investigates the preliminary efficacy of the combination at the established safe dose. Participants must have previously received two or more systemic treatments, including anti-PD-1 monoclonal antibodies, and the trial includes monitoring immunological responses and pharmacokinetics.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18 to 75 with advanced metastatic gastric or gastroesophageal junction adenocarcinoma who have failed multiple prior treatments.

Not a fit: Patients who have not received prior anti-PD-1 monoclonal antibodies or those with early-stage gastric cancer 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: Other studies have shown promising results with similar immunotherapy approaches, suggesting potential for success in this trial.

Eligibility criteria

Inclusion Criteria:

\- (Subjects must meet all of the following inclusion criteria to enter the trial)

1. Subjects must give informed consent to this study before the trial and voluntarily sign a written informed consent form.
2. aged 18 to 75 years (inclusive), male or female.
3. Patients with advanced metastatic gastric or gastroesophageal junction adenocarcinoma confirmed by histopathology or cytology.
4. According to the Guidelines for the Diagnosis and Treatment of Gastric Cancer (CSCO, version 2021), patients must have previously failed two or more systemic treatment regimens (which must include anti-PD-1 monoclonal antibodies), or patients who cannot continue treatment due to severe adverse reactions as judged by the investigator.
5. Be able to provide paraffin blocks and/or tissue sections of previously archived pathological tissues, or willing to undergo tumor tissue biopsy before administration.
6. The presence of at least one measurable CT scan according to RECIST 1.1 and meeting the requirements for an acceptable injection dose volume (or the first injection dose volume in Phase IIa) in the current dose group, tumor metastases that can be injected under ultrasound guidance (injected lesions are best major tumor burden lesions), and the baseline longest diameter of the injected lesion (lymph node lesions are short diameters) \> 1.5 cm.
7. Positive test result for herpes simplex virus I antibodies (HSV-1 IgG or HSV-1 IgM).
8. ECOG performance status score 0-1.
9. Expected survival time of more than 3 months.
10. adequate organ function: 1) blood routine (no blood transfusion or colony-stimulating factor treatment within 14 days): ANC ≥ 1.5 × 10\^9/L, PLT ≥ 100 × 10\^9/L, Hb ≥ 85 g/L, lymphocyte count ≥ 1.5 × 10\^9/L (for lymphocyte count 0.8 × 10\^9/L to 1.5 × 10\^9/L, the investigator judged whether to enroll); 2) liver function: TBIL ≤ 1.5 × ULN, ALT ≤ 3 × ULN, AST ≤ 3 × ULN; 3) renal function: Cr ≤ 1.5 × ULN, and creatinine clearance ≥ 45ml/min (calculated according to Cockcroft-Gault formula); 4) coagulation function: activated partial thromboplastin time (APTT) ≤ 1.5 × ULN, international normalized ratio (INR) ≤ 1.5 × ULN.
11. eligible subjects of childbearing potential (men and women) must agree to use a reliable method of contraception (hormonal or barrier method or abstinence) during the trial and for at least 90 days after the last dose (VG161 or nivolumab, calculated at the later of the day).
12. Female patients of childbearing age must have a negative blood pregnancy test within 1 day prior to enrollment.

Exclusion Criteria:

\- (Any of the following criteria must be excluded)

1. received chemotherapy, radiotherapy, biological therapy, endocrine therapy, targeted therapy, immunotherapy and other anti-tumor drugs within 4 weeks before the first use of the study drug, of which oral fluorouracil and small molecule targeted drugs were within 2 weeks before the first use of the study drug or within 5 half-lives of the drug (whichever was longer).
2. received other unmarketed clinical trial treatment within 4 weeks before the first dose of study drug.
3. Major organ surgery (excluding needle biopsy) or significant trauma within 4 weeks before the first dose of study drug.
4. Patients who have received systemic corticosteroids (prednisone \> 10 mg/day or equivalent doses of the same class of drugs) or other immunosuppressive agents within 14 days before the first dose of study drug; except for the following: topical, ocular, intra-articular, intranasal, and inhaled corticosteroids; short-term corticosteroids (≤ 10 mg prednisone equivalent) for prophylaxis (e.g., prevention of contrast agent allergy).
5. Vaccination within 4 weeks prior to the first dose of study drug.
6. Adverse reactions of previous anti-tumor treatment have not recovered to CTCAE 5.0 grade evaluation ≤ 1 (except alopecia and other toxicities judged by the investigator as having no safety risk).
7. Patients with central nervous system metastasis, spinal cord metastasis and/or spinal cord compression.
8. patients with active diverticulitis or symptomatic gastrointestinal ulcers;
9. in the herpes simplex virus recurrence infection period, and there are corresponding clinical manifestations, such as oral herpes labialis, herpes keratitis herpeticum, genital herpes, etc., or there are herpes infection-related complications (herpes keratitis, encephalitis, nerve injury, etc.), and intermittent or long-term use of anti-herpes drugs (e.g., acyclovir) treatment, except intermittent local use.
10. other active uncontrolled infections.
11. History of immunodeficiency, including positive HIV antibody test and positive Treponema pallidum antibody test.
12. Patients with active chronic hepatitis B or active hepatitis C (except hepatitis B virus carriers, stable hepatitis B after drug treatment \[HBV-DNA test negative or \< 50 IU/ml\] and cured hepatitis C patients \[HCV RNA test negative\]);
13. history of serious cardiovascular disease: 1) ventricular arrhythmia requiring clinical intervention; 2) QTc interval \> 480 ms; 3) Acute coronary syndrome, congestive heart failure, stroke or other Grade III or higher cardiovascular events within 6 months; 4) New York Heart Association (NYHA) functional classification ≥ II or left ventricular ejection fraction (LVEF) \< 40%; 5) uncontrolled hypertension after treatment (as judged by the investigator).
14. Patients with active, or have had and have had autoimmune diseases that may recur (such as interstitial pneumonia, colitis, hepatitis, hypophysitis, vasculitis, nephritis, hyperthyroidism, hypothyroidism, including but not limited to these diseases or syndromes, etc.); but excluding patients with clinically stable autoimmune thyroiditis, autoimmune-mediated hypothyroidism treated with stable doses of thyroid replacement hormone; type I diabetes using stable doses of insulin; vitiligo or recovered childhood asthma/allergy, and patients who do not require any intervention in adulthood.
15. Having received immunotherapy and have experienced immune-related adverse events (irAEs) such as immune-related pneumonia and myocarditis, which may affect the safety of the investigational drug as judged by the investigator.
16. Patients who have received immune checkpoint inhibitors and develop serious adverse reactions after treatment and need to be permanently disabled.
17. Known alcohol or drug dependence.
18. Mental disorders or poor compliance.
19. Pregnant or lactating women.
20. subjects with pleural effusion or pericardial effusion or ascites requiring clinical intervention.
21. The investigator believes that the subject has other serious systemic diseases or other reasons and is not suitable for this clinical study.

Where this trial is running

Beijing, Beijing Municipality

• Peking University Cancer Hospital — Beijing, Beijing Municipality, China (Recruiting)

Study contacts

• Principal investigator: Lin Shen — Peking University Cancer Hospital & Institute
• Study coordinator: Lin Shen, Professor

Conditions Metastatic Gastric Cancer; Gastric cancer