Phase 2 Kidney Cancer Trial, Recruiting NCT07233252 Sponsor: Tianjin Medical University Second Hospital Condition: Kidney Cancer
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Phase 2 Kidney Cancer Trial, Recruiting

NCT07233252
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:

  • Adults aged 18 or older
  • People who are scheduled to have a procedure called ureteroscopic laser ablation to treat a tumour in the renal pelvis (the part of the kidney where urine collects)
  • People whose tumour is in the renal pelvis, has been confirmed as a type of cancer called upper tract urothelial carcinoma through biopsy, urine testing, or imaging scans (such as CT, MRI, or PET-CT), has not spread to lymph nodes or other parts of the body, is at an early-to-intermediate stage (T1–T2N0M0), and measures less than 3 cm across at its widest point
  • People with an expected survival of more than 12 weeks
  • People with a general health and activity level rated 0–2 on a standard medical scale, meaning they are able to carry out at least some daily activities (confirm with trial site)
  • People who agree to provide blood, urine, and tissue samples for laboratory testing during the trial
  • People whose blood counts, liver function, and kidney function meet specific minimum levels as measured by laboratory tests (confirm with trial site for exact values)
  • People who are willing to take part and able to follow the study requirements

Who may not be able to join:

  • People who currently have an active cancer in another part of the body (people with a past cancer that has been treated and is now stable may still be considered)
  • People who have this same type of cancer in both kidneys
  • People who have urothelial cancer in the ureter or bladder, unless the bladder cancer is a non-muscle-invasive type that can be fully removed with a standard bladder procedure
  • People who have received a live attenuated (weakened) vaccine within 4 weeks before starting treatment, or who plan to receive one during the study
  • People with an active or known autoimmune disease, or a suspected history of one
  • People with a known history of a primary immune system deficiency
  • People who have previously received an organ transplant or a stem cell transplant from another person
  • People who are pregnant or breastfeeding
  • People with untreated active Hepatitis B or Hepatitis C infection (people already receiving antiviral treatment with monitored viral levels may be considered at the treating doctor's discretion)
  • People who have taken immune-suppressing medications within 4 weeks before starting treatment, with the exception of certain low-dose or topical steroids (confirm with trial site)
  • People with a known or suspected allergy to the study drugs 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 of reproductive age who are not using effective contraception
  • People with certain serious uncontrolled health conditions, including HIV infection, severe uncontrolled infections, uncontrolled psychiatric or neurological conditions (such as epilepsy or dementia), unstable heart, lung, liver, or kidney disease, uncontrolled high blood pressure, active bleeding or new blood clots, 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 22 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: Hailong Hu, PhD, Tianjin Medical University Second Hospital

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
25 November 2025
Est. completion
30 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

One-year Nephron-Sparing Survival (1-year-NSS)

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: 22 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