Bladder Cancer Trial, Recruiting NCT07379255 Sponsor: Qilu Hospital of Shandong University Condition: Bladder Cancer
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Bladder Cancer Trial, Recruiting

NCT07379255
Recruiting Not Applicable

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 between 18 and 80 years, of any gender
  • People who have had surgery to remove the bladder (radical cystectomy), where tissue from the removed bladder will be used to grow laboratory cell cultures called organoids
  • People whose bladder cancer has been found to have spread beyond the bladder wall or into nearby lymph nodes (stages pT3–pT4 and/or lymph node-positive), and who need chemotherapy after surgery
  • People whose overall health is good enough to tolerate platinum-based chemotherapy (a common type of cancer chemotherapy)
  • People with a general health and activity level rated at 0, 1, or 2 on a standard medical scale, meaning they are able to carry out at least some daily activities (confirm with trial site)
  • People who are willing and able to follow the study plan, attend check-ups, and report any side effects or changes in health
  • People who have understood the study and have signed a consent form agreeing to take part

Who may not be able to join:

  • People who experienced serious, life-threatening complications after bladder removal surgery, such as heart problems, kidney failure, breathing failure, liver failure, severe infection, blood clots in the lungs, or major bleeding
  • People with a weakened immune system, such as those living with AIDS, or those receiving treatments that suppress the immune system or radiotherapy
  • People known to have an allergy to the study drug, similar drugs, or their ingredients, or people who have a history of severe allergic reactions in general
  • People who take corticosteroid medicines long-term, or who have a history of drug misuse or dependence
  • People who are pregnant, breastfeeding, or planning to become pregnant in the near future
  • People whose blood test results fall outside acceptable levels, including low counts of white blood cells, red blood cells, or platelets, abnormal liver or kidney function, or abnormal blood clotting results (confirm with trial site for specific values)
  • People who have ever been diagnosed with certain blood or bone marrow conditions, including myelodysplastic syndrome (MDS) or acute myeloid leukaemia (AML)
  • People with a known history of neurological or psychiatric conditions, such as epilepsy or dementia
  • People with other serious health conditions that could put them at risk or affect their ability to complete the study, such as severe high blood pressure, diabetes, or thyroid disorders
  • People with other serious illnesses that require additional treatment or that have significantly abnormal test results
  • People whose personal or family circumstances could affect their safety or the collection of study data and samples
  • People with ongoing or uncontrolled health conditions, including active infections needing treatment, heart failure with symptoms, unstable chest pain, or irregular heartbeat
  • People considered by the trial doctors to be unsuitable for the study for any other reason

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 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: +86 18560084873

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
Not Applicable
Sponsor
Qilu Hospital of Shandong University
Registry
ClinicalTrials.gov
Start date
1 January 2025
Est. completion
31 December 2030

Where this trial is recruiting

🇨🇳 China

Primary endpoints

One-year OS ,Three-year OS and five-year OS

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: 27 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