Phase 2 Bladder Cancer Trial, Recruiting NCT07025174 Sponsor: First Affiliated Hospital of Zhejiang University Condition: Bladder Cancer
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Phase 2 Bladder Cancer Trial, Recruiting

NCT07025174
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 who are between 18 and 75 years old at the time of joining the trial
  • People who have been diagnosed (confirmed by laboratory testing of tissue or cell samples) with advanced or spread-out bile duct or gallbladder cancer (specifically intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma, or gallbladder carcinoma)
  • People whose cancer cannot be removed by surgery and is not able to be cured
  • People who have at least one tumour that can be measured using standard imaging guidelines
  • People who are reasonably active and able to carry out daily activities, as assessed by a standard medical scoring system (ECOG score of 0 or 1 — confirm with trial site)
  • People who are expected to live for at least 12 weeks
  • People who have not previously received chemotherapy, immunotherapy, or anti-blood-vessel-targeting therapy for their advanced cancer (people who completed a prior preventative course of therapy more than 6 months ago may still be eligible — confirm with trial site)
  • People whose blood counts and bone marrow are working well enough, based on specific blood test results
  • People whose liver is functioning well enough, based on specific blood test results
  • People whose kidneys are functioning well enough, based on specific blood test results
  • People who have read and signed a consent form agreeing to take part

Who may not be able to join:

  • People whose cancer is a mixed tumour type or contains a specific rare cell type called neuroendocrine
  • People who have active cancer spread to the brain or spinal cord (people with previously treated and stable brain metastases for more than 4 weeks may still be considered — confirm with trial site)
  • People who have had another type of cancer in the past 5 years, with some exceptions such as certain treated skin cancers or early-stage cancers that were fully treated
  • People who have an active autoimmune disease (where the immune system attacks the body) that requires ongoing medical treatment
  • People who have had a severe allergic reaction to medicines similar to those used in this trial
  • People with high blood pressure that remains above 140/90 mmHg even with medication
  • People with serious heart conditions, including unstable chest pain, a heart attack within the past 6 months, or significant heart failure
  • People who have active bleeding, a tendency to bleed, blood clots, or who are taking blood-thinning medicines
  • People who have had major surgery in the past 4 weeks or minor surgery in the past 2 weeks
  • People who have an active infection currently being treated with medicines
  • People who are pregnant or breastfeeding
  • People who have HIV, or active hepatitis B or C infection
  • People with a psychiatric condition that may make it difficult to follow the trial requirements

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

Principal Investigator: Tingbo Liang, MD, Department of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine

Phone: 86-571-87235407

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
First Affiliated Hospital of Zhejiang University
Registry
ClinicalTrials.gov
Start date
1 June 2025
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-Free Survival (PFS) of Second-Line Treatment

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