Clinical Study of VG161 in Advanced Intrahepatic Cholangiocarcinoma

A Single-Arm, Multicenter, Open-Label Phase IIa Clinical Study to Evaluate the Efficacy and Safety of VG161 in the Treatment of Advanced Intrahepatic Cholangiocarcinoma

VG161 is a recombinant human-IL12/15/PDL1B oncolytic HSV-1 Injectable. This trial is a single-agent, single-arm, multicenter, open-label design clinical trial for advanced intrahepatic cholangiocarcinoma who have failed standard therapy. To evaluate the efficacy of VG161 administered by ultrasound or CT-guided intratumoral injection in patients with advanced intrahepatic cholangiocarcinoma, with the primary outcome measure being objective response rate (ORR).

Study Overview

• Status: Recruiting
• Conditions: Advanced Intrahepatic Cholangiocarcinoma
• Intervention / Treatment: Drug: Recombinant Human IL12/15-PDL1B Oncolytic HSV-1 Injection (Vero Cell))

Detailed Description

The trial was conducted in two phases, and in the first phase, a total of 20 subjects were enrolled (per efficacy assessment analysis set). If 5 or more of the 20 subjects in Stage I achieve an objective response, i.e., the overall ORR is greater than 4/20, it suggests that the drug warrants further investigation and no additional subjects are required to enter Stage II. If only 1 or no subject out of 20 had an objective response, the trial was stopped, indicating that the trial drug had no apparent effect. Otherwise, continue to enter Stage II, add 13 subjects (as per efficacy evaluation analysis set), and the total number of subjects reaches 33. If 5 or more of 33 subjects achieve objective response, i.e., the overall ORR is greater than 4/33, it indicates that the drug has good anti-tumor efficacy and is worthy of entering confirmatory clinical trials.

• Study Type: Interventional
• Enrollment (Estimated): 33
• Phase: Phase 2

Contacts and Locations

• Study Contact: Name: Tingbo Liang, MD.PhD.; Phone Number: 0571-87236666; Email: liangtingbo@zju.edu.cn

Study Locations

• China
  • Zhejiang
    • Hangzhou, Zhejiang, China
      • Recruiting
      • The First Affiliated Hospital, Zhejiang University School of Medicine
      • Contact: Yinan Shen, MD. PhD.; Email: fysyn@163.com
      • Contact: Tingbo Liang, MD. PhD.

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• 1. Subjects must fully understand and 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 histologically or cytologically confirmed advanced intrahepatic cholangiocarcinoma.

  4. According to the Guidelines for the Diagnosis and Treatment of Biliary Malignant Tumors (CSCO), patients must have previously received at least systemic first-line therapy for advanced intrahepatic cholangiocarcinoma and failed, or cannot tolerate treatment. Patients who received preoperative neoadjuvant chemotherapy or postoperative adjuvant chemotherapy were counted as having failed first-line treatment if disease progression occurred during chemotherapy or within 6 months after stopping chemotherapy; 5. According to RECIST 1.1 criteria, one or more CT examinations are determined to be measurable and meet the requirements for the volume administered for the first injection, tumor lesions and/or metastases (the injected lesions should preferably be the main tumor burden lesions) that can be injected under ultrasound or CT guidance, and the baseline longest diameter of the injected lesions (lymph node lesions are short diameters) is > 1.5 cm.

  6. Herpes simplex virus type I (HSV-1) antibody test results (HSV-1 IgG or HSV-1 IgM) are positive.

  7. ECOG performance score 0-1. 8. Expected survival time of more than 3 months. 9.Adequate organ function:

  1. Blood routine (no blood transfusion or colony-stimulating factor treatment within 14 days): ANC ≥ 1.5 × 109/L, PLT ≥ 75 × 109/L, Hb ≥ 85 g/L;
  2. Liver function: TBIL ≤ 1.5 × ULN, ALT ≤ 3 × ULN, AST ≤ 3 × ULN;
  3. Child-Pugh A-B;
  4. Renal function: Cr ≤ 1.5 × ULN, and creatinine clearance ≥ 45ml/min (calculated according to Cockcroft-Gault formula);

  5. Coagulation function: activated partial thromboplastin time (APTT) ≤ 1.5 × ULN, prothrombin time (PT) ≤ 1.5 × ULN, international normalized ratio (INR) ≤ 1.5 × ULN; 10.Eligible patients 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; female patients of childbearing potential must have a negative blood pregnancy test within 7 days prior to enrollment.

     Exclusion Criteria:

• 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. Patients who have received transcatheter arterial chemoembolization (TACE) within 4 weeks before the first use of the study drug.

  3. Received other clinical trial drugs that are not approved for marketing within 4 weeks before the first use of the study drug.

  4. Major organ surgery (excluding needle biopsy) or significant trauma within 4 weeks before the first dose of study drug.

  5. Have received a vaccine within 4 weeks prior to the first dose of study drug.

  6. 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).

  7. The adverse reactions of previous anti-tumor treatment have not recovered to CTCAE 5.0 grade evaluation ≤ 1 (except alopecia and other toxicities that are judged by the investigator to have no safety risk); 8. Patients with central nervous system metastasis, spinal cord metastasis and/or spinal cord compression.

  9. in the herpes simplex virus recurrence and infection period, and there are corresponding clinical manifestations, such as oral herpes labialis, herpetic keratitis, herpetic dermatitis, genital herpes and so on.

  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, hepatitis B virus stable after drug treatment [HBV-DNA negative or < 500 IU/ml] and cured hepatitis C patients [HCV RNA 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 and above cardiovascular events within 6 months before the first use of study drugs;
  4. New York Heart Association (NYHA) functional classification ≥ II or left ventricular ejection fraction (LVEF) < 40%;
  5. Uncontrolled hypertension after treatment (judged by the investigator); 14. Patients with active, or have had and have the possibility of relapse of autoimmune diseases (such as systemic lupus erythematosus, rheumatoid arthritis, vasculitis, etc.); except for clinically stable autoimmune thyroiditis, autoimmune-mediated hypothyroidism treated with stable doses of thyroid replacement hormone, type I diabetes treated with stable doses of insulin, vitiligo or recovered childhood asthma/allergy, without any intervention in adults.

  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. Known alcohol or drug dependence. 17. Patients with mental disorders or poor compliance. 18. Pregnant or lactating women. 19. The investigator believes that the subject has other serious systemic diseases or other reasons and is not suitable for this clinical study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Single Arm; 1.0 × 10^8 PFU/day per cycle, intratumoral injection for 3 consecutive days in 28-day cycles.	Drug: Recombinant Human IL12/15-PDL1B Oncolytic HSV-1 Injection (Vero Cell)); Intratumoral injection only. The dosing date is Days 1 through 3.; Other Names: VG161

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
ORR	Efficacy evaluation endpoint measures will be evaluated according to iRECIST criteria and refer to RECIST 1.1 criteria.	27 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
PFS	Evaluate medium Progression Free Survival by iRECIST	27 months
6-month survival rates (OS rate)	Evaluate Overall Survival rate	33 months
6-month overall survival (OS)	Overall Survival	33 months
12-month survival rates (OS rate)	Evaluate Overall Survival rate	39 months
12-month overall survival (OS)	Overall Survival	39 months
DOR	Evaluate Disease Control Rate by iRECIST	27 months
peripheral blood lymphocyte subsets (CD3 +, CD4 +, CD8 +, CD4 +/CD8 + ratio, NK, CD19 +, CD56 + cells)	Concentration of CD3+, CD4+, CD8+, CD4 +/CD8 + ratio, NK, CD19 +, CD56 + cells	27 months
cytokines (IL-6, TNF-α, IFN-γ)	Concentration of IL-6, TNF-α, IFN-γ	27 months
T cell-related parameters (PD-L1, PD-1, CD69, CD8 + Ki67high)	Concentration of PD-L1, PD-1, CD69, CD8 + Ki67high	27 months
Safety indicators：laboratory tests results	Incidence of abnormal laboratory tests results	27 months

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Exploratory Endpoints	Single-cell sequencing was performed on tumor biopsy samples to explore biomarkers predictive of clinical response to VG161.	27 months

Collaborators and Investigators

• Sponsor: CNBG-Virogin Biotech (Shanghai) Ltd.
• Investigators: Principal Investigator: Tingbo Liang, Zhejiang University

Study record dates

Study Major Dates

• Study Start (Actual): March 19, 2022
• Primary Completion (Estimated): September 30, 2025
• Study Completion (Estimated): December 1, 2025

Study Registration Dates

• First Submitted: February 19, 2023
• First Submitted That Met QC Criteria: December 19, 2024
• First Posted (Actual): March 25, 2025

Study Record Updates

• Last Update Posted (Actual): March 25, 2025
• Last Update Submitted That Met QC Criteria: December 19, 2024
• Last Verified: December 1, 2024

More Information

Terms related to this study

• Keywords: Advanced intrahepatic cholangiocarcinoma
• Additional Relevant MeSH Terms: Neoplasms; Neoplasms by Histologic Type; Neoplasms, Glandular and Epithelial; Adenocarcinoma; Carcinoma; Cholangiocarcinoma
• Other Study ID Numbers: VG161-C201

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No