Phase 2 Melanoma Trial, Recruiting NCT03842943 Sponsor: University of Louisville Condition: Melanoma
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Phase 2 Melanoma Trial, Recruiting

NCT03842943
Recruiting Phase 2

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 9 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 2
Sponsor
University of Louisville
Registry
ClinicalTrials.gov
Start date
3 July 2019
Est. completion
1 June 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Pathologic Complete Response

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov