Phase 2 Kidney Cancer Trial, Recruiting NCT06690697 Sponsor: Fudan University Condition: Kidney Cancer
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Phase 2 Kidney Cancer Trial, Recruiting

NCT06690697
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 are willing to take part voluntarily, are able to follow the study requirements, and agree to sign a consent form
  • You are 18 years of age or older
  • You have been diagnosed with kidney cancer (renal cell carcinoma) that has come back or spread, and this was confirmed through a tissue biopsy after surgery to remove the original tumour
  • You have already received one type of systemic (whole-body) treatment that either stopped working or caused side effects you could not tolerate, or your cancer came back within 6 months of completing an earlier course of treatment given before or after surgery
  • You are able to provide stored tumour tissue samples from your previous surgery (either a tissue block or at least 20 tissue slices) for testing purposes, and the tissue must show a specific pattern of immune cells called TLS (confirm with trial site)
  • You have at least one area of cancer that can be measured on a scan, according to standard guidelines
  • Your general health and ability to carry out daily activities is rated as good (a score of 0 or 1 on a standard scale used by doctors)
  • Your blood counts, liver function, kidney function, blood clotting, and thyroid hormone levels all meet specific minimum standards set by the trial (confirm exact values with trial site)
  • If you are a woman who could become pregnant, you must confirm you are not pregnant before joining, and all participants must use reliable contraception throughout treatment and for 4 weeks after treatment ends

Who may not be able to join:

  • You have a known allergy to any of the medicines or ingredients used in this trial
  • You have received other cancer treatments, local tumour treatments, or taken part in another clinical trial within the 4 weeks before starting this trial (a shorter gap may be allowed in some cases — confirm with trial site)
  • You have previously been treated with a specific type of drug that targets BTLA or HVEM (confirm with trial site)
  • You have a reason why you cannot take the specific study drugs used in this trial (confirm with trial site)
  • You have had or currently have another type of cancer, unless it was cervical cancer, basal cell skin cancer, or squamous cell skin cancer that has been fully cured
  • You have an active autoimmune disease (where the immune system attacks the body) that has required treatment in the past 3 months, or a history of a severe autoimmune condition, or need to take steroids or immune-suppressing medicines regularly
  • You are known to be HIV positive
  • You are pregnant, breastfeeding, or planning to become pregnant during the study
  • You have a tendency to bleed (for example, from active stomach ulcers) or are taking blood-thinning medicines such as warfarin or heparin
  • You have a history of lung inflammation or scarring (such as interstitial lung disease or radiation damage to the lungs), or there are signs of active lung inflammation on a recent chest scan
  • You have other serious health conditions that your doctor feels could put you at risk or affect the study results

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 16 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: +862164175590

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
1 June 2024
Est. completion
30 June 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall Response Rate (ORR)

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: 16 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