Recruiting nowPhase 1Ages 18 Years and up
IDOV-Immune for Advanced Solid Tumors
Sponsor: ViroMissile, Inc. · NCT06910657 on ClinicalTrials.gov ↗
Conditions studied
Colorectal CancerPancreatic CancerMelanomaOvarian CancerGastric CancerEsophageal CancerHepatocellular CarcinomaRenal Cell CarcinomaBreast CancerSarcomaBladder CancerLung CancerProstate CancerCervical CancersHead and Neck CancersAdrenal Gland Tumors
What it tests
- IDOV-Immune (oncolytic vaccinia virus)biological
Where it's running6 sites
- Opening soon
Washington University School of Medicine
St Louis, Missouri 63110
- Sara Mitchum(contact)314-273-8602[email protected]
- Opening soon
MD Anderson Cancer Center
Houston, Texas 77030
- Investigator(contact)877-632-6789[email protected]
- Recruiting now
South Texas Accelerated Research Therapeutics
San Antonio, Texas 78229
- Investigator(contact)210-593-5250[email protected]
3 international sites
- Opening soon
Royal North Shore Hospital
Saint Leonards, New South Wales, Australia 2065
- Investigator(contact)+61 (02) 9463 1199[email protected]
- Recruiting now
Westmead Hospital
Westmead, New South Wales, Australia 2145
- Investigator(contact)+61 2 8890 9945[email protected]
- Recruiting now
The Alfred Hospital
Melbourne, Victoria, Australia 3004
- Malaka Ameratunga, MD, PhD(contact)+61 03 9076 3129[email protected]
See the official eligibility language
Shown exactly as written on ClinicalTrials.gov. Your oncologist is the right person to judge whether it fits your situation.
Key Inclusion Criteria: * Age ≥ 18 years. * Histologically or cytologically confirmed advanced solid tumors that have progressed despite standard therapy, or for which no standard therapy exists. * ECOG performance status ≤ 1. * Measurable disease per RECIST v1.1. * Adequate organ and bone marrow function. * At least 28 days since major surgery, prior immunotherapy, or radiotherapy (with exceptions for minor procedures). * Negative pregnancy test for women of childbearing potential. * Agreement to use effective contraception during treatment and for 3 months after. * Ability to provide informed consent and comply with study requirements. Key Exclusion Criteria: * Prior treatment with an oncolytic virus. * Active or recent vaccinia virus infection or smallpox/monkeypox vaccination within 10 years. * Active uncontrolled infection requiring systemic treatment. * History of hepatitis B, hepatitis C, or HIV (unless meeting protocol-specific criteria). * Unresolved ≥ Grade 2 toxicities from prior therapies (except hair loss or stable chronic conditions). * Active or symptomatic autoimmune disease requiring systemic therapy. * Active or untreated CNS metastases (unless stable per protocol). * Significant cardiac disease (e.g., NYHA Class III/IV heart failure). * Interstitial lung disease or prior pneumonitis requiring steroids. * Conditions requiring chronic immunosuppressive therapy. * Severe skin disorders or history of pancreatitis. * Bleeding disorders or history of recent serious thromboembolic events. * Any medical or psychiatric condition that could interfere with study participation.
Updated 2026-03-02 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.