Phase 3 Bladder Cancer Trial, Recruiting NCT07106762 Sponsor: Bristol-Myers Squibb Condition: Bladder Cancer
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Phase 3 Bladder Cancer Trial, Recruiting

NCT07106762
Recruiting Phase 3 🇦🇺 Australian site

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 have been diagnosed with advanced bladder or urinary tract cancer that has been confirmed by a lab test (biopsy).
  • You are able to receive a type of chemotherapy that contains platinum (such as cisplatin or carboplatin).
  • You have previously been treated with a type of immunotherapy drug called an anti-PD-(L)1 therapy (for example, pembrolizumab or atezolizumab) for advanced or spreading cancer.
  • If your immunotherapy was given around the time of surgery, your cancer must have come back within 12 months of your last dose.
  • You have at least one area of cancer that can be measured on a scan.
  • You are generally well enough to carry out light activity and care for yourself (confirm with trial site for exact fitness level required).

Who may not be able to join:

  • You have received platinum-based chemotherapy within the last 12 months.
  • You have already had more than 2 different cancer treatment regimens in total.
  • You have previously received a type of targeted drug therapy (called an ADC) that targets EGFR or HER3.
  • You have previously been treated with a drug that belongs to a group called topoisomerase 1 inhibitors (confirm with trial site for specific examples).
  • You currently have cancer that has spread to the brain and is not being treated.
  • There are additional criteria set by the trial team that may also affect eligibility (confirm with trial site).

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 5 July 2026
Phase 3: approximately ~65% 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: Bristol-Myers Squibb, Bristol-Myers Squibb

Phone: 855-907-3286

Australian sites

Macquarie University, Macquarie University, New South Wales
+61298122956
GenesisCare North Shore, St Leonards, New South Wales
61294631172
Austin Health, Heidelberg, Victoria
+61394965000

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 3
Registry
ClinicalTrials.gov
Start date
30 September 2025
Est. completion
26 January 2029

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇦🇹 Austria 🇧🇪 Belgium 🇧🇷 Brazil 🇨🇦 Canada 🇨🇳 China 🇨🇿 Czechia 🇫🇷 France 🇩🇪 Germany 🇮🇪 Ireland 🇮🇱 Israel 🇮🇹 Italy 🇯🇵 Japan 🇳🇱 Netherlands 🇳🇴 Norway 🇷🇴 Romania 🇪🇸 Spain 🇸🇪 Sweden 🇨🇭 Switzerland 🇬🇧 United Kingdom 🇺🇸 United States

3 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Phase 2: Recommended Phase 3 Dose (RP3D) of BMS-986507; Phase 3: Progression-Free Survival (PFS); Phase 3: Overall Survival (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: 5 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