A Clinical Study to Evaluate the Efficacy and Safety of VG2025 in Intrahepatic Cholangiocarcinoma

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorVirogin Biotech Ltd.

About this trial

VG2025 is a Recombinant Human IL12/15 Dual-Regulated Oncolytic HSV-1 Injection. Currently, one phase I dose escalation safety study has been completed in China and the United States respectively, both demonstrating excellent safety profiles with no dose-limiting toxicities (DLTs) observed and no maximum tolerated dose (MTD) identified. Moreover, it has shown preliminary efficacy in treating advanced tumors. Considering the actual clinical needs and the volume of intratumoral administration, a more appropriate recommended phase 2 dose (RP2D) level has been selected for the phase II clinical trial.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Signed written informed consent form.

Age 18 to 75 years (inclusive), male or female.

Histologically or cytologically confirmed advanced intrahepatic cholangiocarcinoma.

Eligible participants of childbearing participants(male and female) must agree to use a reliable method of contraception during the trial and for at least 90 days after dosing; females of childbearing potential must have a negative blood pregnancy test 7 days before enrollment.

Disqualifiers

Participants who have received other unlisted drugs clinical trial treatment 4 weeks before the first dose of the study drug.

Participants who underwent major organ surgery (excluding needle biopsy) or had significant trauma 4 weeks before the first dose of the study drug.

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.

Other active uncontrolled infection.

Trial design

Design model

Single group

Treatments tested in this trial

  • VG2025

    Drug

    Recommended Phase II Dose, Intratumoral Injection, Q4W

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: Single ArmExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

ORR

Objective response rate (ORR)

Time frame
up to 36 months
2

DCR

Disease control rate (DCR)

Time frame
up to 36 months

Secondary outcomes

1

PFS

Progression-free survival (PFS)

Time frame
up to 36 months
2

OS

Overall Survival (OS)

Time frame
up to 36 months
3

Correlation between VG2025 efficacy and CEA levels

Preliminary analysis of the correlation between the efficacy of VG2025 and peripheral blood carcinoembryonic antigen (CEA) levels

Time frame
up to 36 months
4

Immune-related indicators

Peripheral blood lymphocyte subsets, plasma cytokines, T cell immunity, and other immune-related indicators

Time frame
up to 36 months

Other outcomes

Sponsors and contacts

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