Actively Recruiting

Phase 1
Phase 2
Age: 18Years - 75Years
All Genders
NCT06758544

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

Led by Guangdong Provincial People's Hospital · Updated on 2025-08-17

18

Participants Needed

1

Research Sites

89 weeks

Total Duration

On this page

Sponsors

G

Guangdong Provincial People's Hospital

Lead Sponsor

G

Guangzhou Virotech Pharmaceutical Co., Ltd.

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subject voluntarily agrees to participate and signs informed consent before screening
  • Male or female aged 18 to 75 years at screening
  • Clinical diagnosis of pancreatic cancer
  • Eastern Cooperative Oncology Group (ECOG) score of 0 or 1
  • Expected survival time of at least 6 months
  • No serious blood, heart, liver, kidney, or coagulation problems
Not Eligible

You will not qualify if you...

  • Previous treatment with oncolytic virus or systemic therapy for pancreatic cancer
  • Prior allogeneic hematopoietic stem cell or organ transplantation
  • Immunocompromised condition
  • Known alcohol or drug dependency
  • Pregnant or breastfeeding women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Guangdong Provincial People's Hospital

Guangzhou, Guangdong, China

Actively Recruiting

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Research Team

C

Chen RF Prof.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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