Phase 2 Kidney Cancer Trial, Recruiting
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.
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
Where this trial is recruiting
Primary endpoints
Frequency and severity of treatment-related adverse events; Response rate
Can't join this trial?
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.