Phase 3 Melanoma Trial, Recruiting NCT07530887 Sponsor: Marieke Goodijk Condition: Melanoma
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Phase 3 Melanoma Trial, Recruiting

NCT07530887
Recruiting Phase 3

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:

  • People who are 18 years of age or older at the time of giving consent
  • People whose general health and ability to carry out daily activities falls within a certain range, as measured by a standard medical scoring tool called the ECOG scale (scores 0–2, meaning fully active to capable of self-care) (confirm with trial site)
  • People who have been diagnosed with a specific type of skin melanoma — either Superficial Spreading Melanoma or Nodular Melanoma — confirmed by laboratory analysis of tissue, at a stage between pT1b and pT4b according to a standard medical staging system
  • People whose melanoma was fully removed by a diagnostic surgical excision with at least 1 mm of clear (tumour-free) tissue around the entire removal, including any melanoma that had not yet grown deep into the skin
  • People who are willing and able to follow the treatment plan and attend follow-up appointments, and who have given their informed consent to participate
  • People whose general health (not counting the current melanoma) means a doctor estimates they are likely to live at least 5 more years
  • People who have had a previous cancer may still be considered, provided that: all previous cancers were treated with the intention of curing them, their expected lifespan is at least 5 years, and their treating doctor considers them to be at low risk of that previous cancer returning

Who may not be able to join:

  • People whose melanoma started somewhere other than the skin, such as in the eye or in mucous membranes (for example, mouth or nasal passages)
  • People with acral melanoma (a type found on the palms, soles, or under nails)
  • People with a type of melanoma called Lentigo Maligna Melanoma
  • People with desmoplastic melanoma
  • People with neurotropic melanoma (a type that tends to spread along nerves)
  • People with Spitz melanoma or malignant Spitz tumour
  • People whose melanoma has already spread to nearby skin or lymph nodes, or where visible spread to other parts of the body has been detected
  • People where the diagnosis of melanoma is uncertain — for example, lesions described as being of unknown malignant potential
  • People with a melanoma subtype other than Superficial Spreading Melanoma or Nodular Melanoma
  • People whose melanoma was removed using a shave excision, a scraping technique, or a core biopsy (rather than a full surgical excision)
  • People who have already had reconstructive surgery using a local skin flap at the site where the melanoma was removed
  • People who have a history of a previous or second separate invasive melanoma
  • People with more than one melanoma
  • People who have previously had lymph node removal surgery in the area likely to drain from the melanoma site, unless that surgery was a sentinel lymph node biopsy only
  • People who have had any other cancer (solid tumour or blood cancer) in the past 5 years where life expectancy is estimated at less than 5 years
  • People who have had an organ transplant

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 22 July 2026
Phase 3: approximately ~65% 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

Phone: 020 512 9111

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 3
Sponsor
Marieke Goodijk
Registry
ClinicalTrials.gov
Start date
13 November 2025
Est. completion
1 November 2033

Where this trial is recruiting

🇳🇱 Netherlands

Primary endpoints

Relapse-Free Survival (RFS)

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: 22 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