Phase 2 Melanoma Trial, Recruiting NCT01898039 Sponsor: Hadassah Medical Organization Condition: Melanoma
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Phase 2 Melanoma Trial, Recruiting

NCT01898039
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 must carry at least one of certain specific genetic tissue markers (called HLA types: A2, A24, A33, B35, B49, or CW04/12) — the trial team will test for these (confirm with trial site).
  • You have been diagnosed with skin melanoma that is at a certain stage of seriousness (thick tumors over 4mm, or ulcerated tumors over 4mm).
  • You have melanoma that has spread to nearby lymph nodes and those lymph nodes have been surgically removed.
  • You have melanoma that has spread to distant parts of the body but has been completely removed by surgery.
  • You have melanoma that has spread but cannot be fully removed by surgery, your disease is at a low level, your LDH blood levels are normal, and you have already tried at least two types of treatment (confirm with trial site).
  • You have a non-skin form of melanoma, such as eye (uveal) or mucosal melanoma, at the relevant stages.
  • Your melanoma can have either the BRAF gene mutation or not — both are eligible.
  • You are generally well enough to carry out normal activities, even if some effort is required (Karnofsky score above 80).
  • You do not have any active heart or breathing conditions.
  • You are not pregnant or breastfeeding, and women must use contraception during treatment.
  • Your basic blood count results (red and white blood cells) meet minimum levels.
  • You are willing and able to give your informed consent to participate.

Who may not be able to join:

  • You have received chemotherapy or extensive radiotherapy within the last 28 days.
  • You have active cancer that has spread to the brain and currently requires steroid medication to manage it.
  • You have another active cancer at the same time (except certain minor skin cancers, early-stage cervical abnormalities, or early-stage prostate cancer).
  • You have a serious active infection.
  • You have an allergy to penicillin.
  • You do not wish to continue participating in the study.
  • You are a carrier of HIV, or have chronic Hepatitis B or Hepatitis C.

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 19 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

Phone: 972507874292

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
Hadassah Medical Organization
Registry
ClinicalTrials.gov
Start date
1 May 2013
Est. completion
1 April 2027

Where this trial is recruiting

🇮🇱 Israel

Primary endpoints

grade 2-4 adverse events according to CTCEA criteria; monitoring anti-tumor immune response; grade 2-4 adverse events according to CTCEA criteria; grade 2-4 adverse events according to CTCEA criteria; grade 2-4 adverse events according to CTCEA criteria; grade 2-4 adverse events according to CTCEA criteria; grade 2-4 adverse events according to CTCEA criteria; grade 2-4 adverse events according to CTCEA criteria; monitoring anti-tumor immune response; monitoring anti-tumor immune response; monitoring anti-tumor immune response; monitoring anti-tumor immune response; monitoring anti-tumor immun...

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: 19 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