Phase 2 Kidney Cancer Trial, Recruiting NCT02830724 Sponsor: National Cancer Institute (NCI) Condition: Kidney Cancer
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Phase 2 Kidney Cancer Trial, Recruiting

NCT02830724
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:

  • Your cancer cannot be surgically removed and must test positive for a specific protein called CD70 at a certain level, based on a lab test of cancer tissue.
  • Your cancer diagnosis must be confirmed by the NCI Laboratory of Pathology.
  • You must have already tried at least one standard treatment for your cancer (if one was available), and either your cancer did not respond or it came back.
  • If you have 3 or fewer small tumors in the brain (each no bigger than 1 cm) that are not causing symptoms, you may still be eligible — including if those tumors were previously treated or surgically removed (confirm with trial site).
  • You must be between 18 and 72 years old.
  • You must be well enough to carry out daily activities with little or no limitation (this is measured on a standard scale called ECOG 0 or 1).
  • Both men and women must be willing to use birth control during the study and for 12 months after treatment ends (for women) or 4 months after treatment ends (for men).
  • Women who could become pregnant must be willing to take a pregnancy test before starting treatment.
  • You must test negative for HIV.
  • You must test negative for hepatitis B and hepatitis C (if a hepatitis C screening test comes back positive, a further test must confirm you do not have an active infection).
  • Your blood cell counts must meet certain minimum levels: enough white blood cells, infection-fighting cells (neutrophils), platelets, and red blood cells (a blood transfusion may be allowed to meet the red blood cell requirement).
  • Your liver and kidney function must be within acceptable ranges based on blood tests.
  • Any previous cancer treatment must be fully completed before you join the trial.
  • You must be able to understand and be willing to sign a written consent form agreeing to take part.
  • You must be willing to sign a document that names someone to make decisions on your behalf if needed (durable power of attorney).
  • You must also be enrolled in a related NCI study for cell collection (protocol 03-C-0277).

Who may not be able to join:

  • Women who are pregnant or breastfeeding.
  • People currently taking steroid medications on an ongoing basis.
  • People with active infections requiring treatment, blood clotting disorders, or other serious uncontrolled health conditions.
  • People with a condition where the immune system does not work properly from birth (such as Severe Combined Immunodeficiency Disease).
  • People with a history of immune system diseases affecting blood cells, or any autoimmune disease that requires medication to suppress the immune system.
  • People with active opportunistic infections (infections that occur when the immune system is weakened).
  • People who have had a severe allergic reaction to any of the drugs used in this trial: cyclophosphamide, fludarabine, or aldesleukin.
  • People with a history of heart bypass surgery or symptoms of reduced blood flow to the heart.
  • People whose heart pumping function is significantly reduced (45% or below), if a heart evaluation was done based on their medical history (confirm with trial site).
  • People whose lung breathing capacity is significantly reduced (50% or below of the expected level), if a lung evaluation was done based on their medical history (confirm with trial site).
  • People currently taking part in another clinical drug trial.

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 26 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: James C Yang, M.D., National Cancer Institute (NCI)

Phone: (866) 820-4505

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
Registry
ClinicalTrials.gov
Start date
6 April 2017
Est. completion
1 January 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Frequency and severity of treatment-related adverse events; Response rate

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: 26 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