Phase 2 Melanoma Trial, Recruiting NCT07193966 Sponsor: Shenzhen Geno-Immune Medical Institute Condition: Melanoma
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Phase 2 Melanoma Trial, Recruiting

NCT07193966
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:

  • People whose cancer has already received standard first-line treatment and has been confirmed as unable to be removed by surgery, has spread to other parts of the body, has continued to grow, or has come back.
  • People whose tumor has been tested and shows positive expression of specific proteins called NG2 and DLL3, confirmed through laboratory testing of tumor tissue or cells.
  • People who weigh at least 40 kg (approximately 88 pounds).
  • People aged 18 to 75 years old at the time of joining the trial.
  • People with a life expectancy of at least 8 weeks.
  • People whose serious side effects from any previous cancer treatment have reduced to a mild-to-moderate level (grade 2 or lower).
  • People who have not received blood cell growth-stimulating injections for at least 1 week before a specific cell collection procedure.
  • People for whom at least 7 days have passed since completing certain targeted cancer therapies or low-dose chemotherapy regimens.
  • People for whom at least 4 weeks have passed since receiving a monoclonal antibody treatment.
  • People for whom at least 1 week has passed since any radiation therapy.
  • People who are in a reasonably good general physical condition, as measured by a standard performance score of 70% or higher (confirm with trial site).
  • People whose heart pumping function meets a minimum threshold, as measured by a specific heart scan (confirm with trial site).
  • People whose blood oxygen level on room air is 90% or above.
  • People whose liver function blood test results are within acceptable ranges as defined by the trial (confirm with trial site).
  • People whose kidney function blood test results are within acceptable ranges as defined by the trial (confirm with trial site).
  • People whose blood cell counts meet minimum levels, including white blood cells, infection-fighting cells, immune cells, and platelets — where the platelet count has not been achieved through a transfusion.
  • People with cancer that has spread to the bone marrow may still be considered, provided their blood count results meet the required levels.
  • People for whom a parent or legal guardian has signed the required consent and agreement forms on their behalf.

Who may not be able to join:

  • People with serious existing illness affecting major organs such as the heart, lungs, or liver, or with significant loss of function in a major organ (except for certain blood-related side effects at a specific grade level).
  • People with untreated cancer that has spread to the brain or spinal cord — though people whose brain or spinal cord involvement has been treated and has been stable for at least 6 weeks may still be considered.
  • People who have previously received a different type of genetically engineered CAR T cell therapy.
  • People with an active HIV, Hepatitis B, or Hepatitis C infection, or any other infection that is not currently under control.
  • People who require ongoing steroid medication or other treatments that suppress the immune system.
  • People whose tumor appears to be at risk of blocking the airway.
  • People who would not be able to follow the requirements of the trial.
  • People for whom an insufficient number of the specialised CAR T cells can be produced for treatment.

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 14 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: +86 0755-86573763

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
Shenzhen Geno-Immune Medical Institute
Registry
ClinicalTrials.gov
Start date
1 September 2025
Est. completion
31 December 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Number of patients with adverse events.

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: 14 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