A Single-arm, Open-label Clinical Study to Evaluate the Efficacy and Safety of VRT106 in Combination With Chemotherapy for Resectable Pancreatic Cancer

Last updated: August 13, 2025
Sponsor: Guangdong Provincial People's Hospital
Overall Status: Active - Recruiting

Phase

1/2

Condition

Pancreatitis

Pancreatic Cancer

Pancreatic Disorders

Treatment

Chemotherapy

Oncolytic virus VRT106

Clinical Study ID

NCT06758544
VRT106-C05
  • Ages 18-75
  • All Genders

Study Summary

This is a single-center, single-arm, open investigator-initiated clinical study to evaluate the efficacy and safety of VRT106 in combination with chemotherapy in the treatment of resectable pancreatic cancer.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Subject voluntarily agrees to participate in this study and signs an InstitutionalReview Board -approved informed consent prior to performing any of the ScreeningVisit procedures.

  2. Males and females at 18-75 years of age, inclusive, at the Screening Visit.

  3. Have a clinical diagnosis of pancreatic cancer.

  4. An Eastern Cooperative Oncology Group (ECOG) score of 0 or 1.

  5. Expected survival time of≥6 months.

  6. No serious hematologic and cardiac abnormalities of the liver, kidneys, orcoagulation functions.

Exclusion

Exclusion Criteria:

  1. Prior treatment with other oncolytic virus or systemic therapy for pancreaticcancer.

  2. Previous allogeneic hematopoietic stem cell transplantation or organtransplantation.

  3. Immunocompromised patients.

  4. Known alcohol or drug dependency.

  5. Women who are pregnant or breastfeeding.

Study Design

Total Participants: 18
Treatment Group(s): 2
Primary Treatment: Chemotherapy
Phase: 1/2
Study Start date:
March 17, 2025
Estimated Completion Date:
November 30, 2026

Study Description

This is a single-center, single-arm, open investigator-initiated clinical study to evaluate the efficacy and safety of VRT106 in combination with chemotherapy in the treatment of resectable pancreatic cancer.

The study is planned to enroll 18 subjects. The entire study consists of a screening period of up to 28 days, treatment period, and a follow-up period (safety follow-up 28 days after the final study dose and survival follow-up once every 3 months).

Connect with a study center

  • Guangdong Provincial People's Hospital

    Guangzhou, Guangdong
    China

    Active - Recruiting

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.