Phase 1 Kidney Cancer Trial, Recruiting NCT07647744 Sponsor: Hrain Biotechnology Co., Ltd. Condition: Kidney Cancer
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Phase 1 Kidney Cancer Trial, Recruiting

NCT07647744
Recruiting Phase 1

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 are between 18 and 70 years old (inclusive), regardless of gender
  • Your doctor expects you to live for more than 12 weeks
  • You are generally able to carry out normal daily activities, or have only mild limitations due to your illness (confirm with trial site)
  • You have been diagnosed with advanced or spreading kidney cancer (specifically the "clear cell" type) that is considered intermediate or high risk by your doctor
  • You have at least one area of cancer that can be measured on a scan
  • A biopsy or tissue sample from your tumor has tested positive for a protein called CD70
  • You have already received at least one previous treatment for your kidney cancer, which must have included either a combination of two immunotherapy drugs targeting PD-1 and CTLA-4, or an immunotherapy drug combined with a targeted therapy aimed at blood vessel growth
  • You have suitable veins for a blood collection procedure, and your blood counts (red cells, white cells, and platelets) meet minimum levels set by the trial
  • Your kidneys, liver, heart, and lungs are working well enough to meet specific test thresholds set by the trial (confirm exact values with trial site)
  • You are willing to take part voluntarily, have understood the study information, and have signed a consent form agreeing to follow all study procedures

Who may not be able to join:

  • You have previously received a treatment that specifically targets CD70
  • Your kidney cancer has spread to your brain
  • You currently have another cancer that is not under control (some early-stage or surgically treated cancers may be exceptions — confirm with trial site)
  • You have an active infection that is not controlled, or you have needed intravenous antibiotics or other infection treatments in the 14 days before joining the trial
  • You have active hepatitis B, hepatitis C, HIV, or syphilis based on blood tests
  • You have certain unstable or serious health conditions, such as recent heart attack or stroke (within the last 6 months), severe heart failure, poorly controlled diabetes, serious irregular heartbeat, or poorly controlled liver, kidney, or metabolic disease
  • You are pregnant, currently breastfeeding, or planning to become pregnant within one year after receiving the treatment — or your partner is planning a pregnancy within that time (unless you are willing to use highly effective contraception throughout)
  • You have previously been treated with CAR-T therapy or any other type of genetically modified cell therapy
  • You have a cardiac pacemaker or a deep brain stimulator implanted
  • You have received a live vaccine within 4 weeks before the blood collection procedure
  • You have had an autoimmune disease (such as Crohn's disease, rheumatoid arthritis, or lupus) in the past 2 years that caused organ damage or required immune-suppressing medication
  • You have a history of significant brain or nervous system conditions, such as seizures, stroke, severe brain injury, dementia, Parkinson's disease, or serious psychiatric disorders
  • You are currently taking steroid tablets or injections and are expected to need them long-term during the study (inhaled or skin-applied steroids may be acceptable — confirm with trial site)
  • You have a condition that would prevent you from understanding or signing the consent form, or from following the study requirements
  • You have had a severe allergic reaction to any medication that would be used in this study
  • Your doctor believes there is any other reason that makes it unsafe or unsuitable for you to take part

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 23 July 2026
Phase 1: approximately ~10% 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: 86-21-58552006

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 1
Sponsor
Hrain Biotechnology Co., Ltd.
Registry
ClinicalTrials.gov
Start date
30 June 2026
Est. completion
1 June 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Dose limited toxicity (DLT)

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: 23 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