Phase 1 Study of VG2025 for Advanced Solid Tumors

This is a Phase 1 study testing a new treatment called VG2025, alone and in combination with nivolumab (Opdivo), for people with advanced solid tumors. These are cancers that have spread or returned, or for which standard treatments haven't worked. The study aims to find the safest dose of VG2025 and understand its side effects. VG2025 is an immunotherapy, meaning it works by using your body's immune system to fight cancer. You could be eligible if you are 18 or older, have a good performance status (meaning you can perform daily activities), and have advanced solid tumors. The study is currently unclear on its recruitment status and plans to enroll 12 participants.

Study design
This is a Phase 1, open-label study, meaning both you and your doctors will know which treatment you are receiving. It uses a dose-escalation design to find the right dose.
What's involved
You would receive VG2025 as injections into your tumor on specific days, either alone or with nivolumab. The treatment schedule varies depending on whether you are in the monotherapy or combination arm.
Compensation
Not stated in the trial record.
Follow-up
The study will track side effects and the maximum tolerated dose for 12 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05266612

Phase I Study VG2025 as a Single Agent and in Combination Therapy With Nivolumab in Subjects With Advanced Malignant Solid Tumors

UNKNOWN
PHASE1Ages 18+InterventionalTreatment
Virogin Biotech Canada Ltd
~12 participants
Updated 2024-08-09 on ClinicalTrials.gov
What's tested:VG2025Nivolumab Injection [Opdivo]

At a glance

Recruiting sites
2 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of Adverse Events
Measured over 12 months
+1 more outcome measured
Solid Tumor

NCT05266612

Where you'd take part

This study runs at 2 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Banner MD Anderson Cancer Center

    Gilbert, Arizonastudy coordinator listed

    Recruiting

  • MD Anderson

    Houston, Texasstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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  • Incidence of Adverse Events12 months

    Incidence of Adverse Events as assessed by National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE), version 5.0

  • MTD12 months

    Recommended Phase 2 Dose