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IDOV-Immune for Advanced Solid Tumors

StatusRecruiting
PhasePhase 1
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Minor Site details revised at 1 of 5 sitesv12
  2. Minor Study sites: 6 to 5v11
  3. Minor Site details revised at 1 of 6 sitesv10
  4. Minor Site details revised at 1 of 6 sitesv9
  5. Notable Primary endpoints revised (4)
    • Secondary endpoints: 9 to 8
    v8
Show 6 earlier versionsHide 6 earlier versions
  1. Minor Site details revised at 1 of 6 sitesv7
  2. Minor Site contacts updated at 1 of 6 sitesv6
  3. Minor Site contacts updated at 1 of 6 sitesv5
  4. Minor Site contacts updated at 1 of 6 sitesv4
  5. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 5 to 6
    • Start date changed from estimate of Jun 1, 2025 to Aug 25, 2025
    v3
  6. Minor Study title shortened, about 12 wordsv2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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This is a Phase I clinical trial evaluating an investigational treatment called IDOV-Immune, a type of oncolytic virus therapy, for adults with advanced solid tumors that have not responded to standard treatments. Oncolytic viruses are designed to infect and destroy cancer cells and have the potential to stimulate the immune system to fight the tumor. The purpose of this study is to determine the safety of IDOV-Immune, how well it is tolerated, and to identify the highest dose that can be safely given. Researchers will also study how the drug behaves in the body, how the immune system responds to it, and whether it shows any signs of shrinking tumors. Participants will receive a single intravenous (IV) infusion of IDOV-Immune and will be closely monitored for side effects and any changes in their cancer. This study is being conducted at multiple sites in the United States and Australia.
Trial Details
NCT Number NCT06910657
Lead Sponsor ViroMissile, Inc.
Conditions
(from sponsor)
Colorectal Cancer, Pancreatic Cancer, Melanoma, Ovarian Cancer, Gastric Cancer, Esophageal Cancer, Hepatocellular Carcinoma, Renal Cell Carcinoma +8 more
Related terms Adrenal Gland Neoplasms, Breast Neoplasms, Carcinoma, Hepatocellular, Carcinoma, Renal Cell, Colorectal Neoplasms, Esophageal Neoplasms, Head and Neck Neoplasms, Lung Neoplasms, Melanoma, Neoplasm Metastasis, Neoplasms, Ovarian Neoplasms, Pancreatic Neoplasms, Prostatic Neoplasms, Sarcoma, Stomach Neoplasms, Urinary Bladder Neoplasms, Uterine Cervical Neoplasms, Vaccinia
Enrollment 78 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov