Phase 2 Melanoma Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are 18 years of age or older, of any race or sex, and have been diagnosed with skin melanoma confirmed by a medical test (such as a biopsy)
- You are generally able to carry out daily activities with little to no limitation (your doctor will assess this using a standard scale)
- Your blood, liver, kidney, and clotting functions are at healthy enough levels (your doctor will check this with tests)
- You have measurable areas of melanoma and have at least one lymph node that can be injected as part of the treatment
- Your original (primary) melanoma tumour has already been surgically removed
- Your melanoma is at stage III and a surgeon who specialises in melanoma has confirmed it can be operated on
- Your stage III melanoma can either be a new diagnosis or a return of melanoma that was previously treated at an earlier stage (stage I or II)
- You may have any type of BRAF gene status — this does not need to be known before joining
- You are willing and able to sign a consent form agreeing to take part
Who may not be able to join:
- You have melanoma that has spread to distant parts of the body (stage M1/metastatic melanoma)
- Your melanoma started in the mucous membranes (such as the mouth or nasal passages) or in the eye
- You have a history of another cancer (other than common skin cancer) within the past 3 years, or your melanoma is linked to a weakened immune system
- You have previously been treated with T-VEC, any other oncolytic virus therapy, pembrolizumab, or any similar immune checkpoint drug targeting PD-1, PD-L1, or PD-L2
- You have a history of certain autoimmune conditions affecting the lungs, kidneys, or blood vessels, or any autoimmune disease that required ongoing medical treatment in the past two years — though vitiligo or childhood asthma that has fully resolved may be acceptable (confirm with trial site)
- You currently have active cold sore or herpes-related skin outbreaks, have had serious complications from a herpes infection in the past, or regularly need antiviral medication (such as acyclovir) to manage herpes — occasional use of a topical antiviral cream may be acceptable (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Michael Egger, MD, University of Louisville
Phone: 502-629-6950
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Pathologic Complete Response
Can't join this trial?
Data last synced from ClinicalTrials.gov: 9 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.