Phase 2 Kidney Cancer Trial, Recruiting NCT07125547 Sponsor: Tianjin Medical University Second Hospital Condition: Kidney Cancer
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Phase 2 Kidney Cancer Trial, Recruiting

NCT07125547
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 aged 18 years or older
  • People who have been diagnosed with cancer of the ureter, confirmed by a scope procedure (ureteroscopy) and imaging scans (such as CT, MRI, or PET-CT), with no signs that the cancer has spread to other parts of the body
  • People whose biopsy results show that more than half of the cancer tissue is a type called urothelial carcinoma
  • People whose medical team has determined that a specific surgical procedure to remove part of the ureter and reconnect the urinary system is appropriate and planned for them
  • People whose expected survival is more than 12 weeks
  • People who have a general health and activity level rated at 0, 1, or 2 on a standard medical scale (meaning able to carry out at least some daily activities independently)
  • People who agree to provide blood, urine, and tissue samples for laboratory testing during the trial
  • People whose blood cell counts, liver function, and kidney function meet specific minimum levels set by the trial (confirm with trial site for exact values)
  • People who are willing to take part and are able to follow the study requirements

Who may not be able to join:

  • People who currently have another active cancer in a different part of the body (people with a previous cancer that has been treated and is now stable may still be considered)
  • People who have urothelial cancer affecting both ureters
  • People who also have urothelial cancer in the kidney's collecting area (renal pelvis) or in the bladder, unless it is an early-stage bladder cancer that can be fully removed by a standard bladder procedure
  • People who have received a live vaccine within 4 weeks before starting the trial, or who plan to receive one during the study
  • People who have an active or known autoimmune disease (a condition where the immune system attacks the body)
  • People with a known history of a primary immune system deficiency
  • People who have previously received an organ transplant or a bone marrow/stem cell transplant from another person
  • People who are pregnant or breastfeeding
  • People with untreated active Hepatitis B or Hepatitis C infection (people receiving antiviral treatment and whose virus levels are being monitored may be considered at the treating doctor's discretion)
  • People who have been taking immune-suppressing medications within 4 weeks before starting the trial, with some exceptions for low-dose or topical steroids (confirm with trial site)
  • People with a known allergy to either of the study medications, Tislelizumab or Nab-Paclitaxel
  • People with active tuberculosis
  • People who have previously been treated with certain types of immunotherapy drugs (PD-1, PD-L1, or CTLA-4 inhibitors)
  • People who are currently taking part in another clinical trial
  • People who are capable of having children and are not using effective contraception
  • People with certain serious uncontrolled health conditions, including HIV infection, severe uncontrolled infections, uncontrolled heart or lung or liver or kidney disease, severe neurological or psychiatric conditions, uncontrolled high blood pressure, active bleeding or new blood clotting problems, or kidney failure requiring dialysis

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 28 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 13662096232

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
Tianjin Medical University Second Hospital
Registry
ClinicalTrials.gov
Start date
5 July 2025
Est. completion
30 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathological Complete Response (pCR)

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: 28 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