Phase 2 Bladder Cancer Trial, Recruiting NCT06704191 Sponsor: Mayo Clinic Condition: Bladder Cancer
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Phase 2 Bladder Cancer Trial, Recruiting

NCT06704191
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:

  • (Phase 1b only) People of any gender who have been diagnosed with non-muscle invasive bladder cancer (an early stage of bladder cancer that has not spread into the bladder muscle, classified as stage Ta, Tis, or T1) and are currently in the early treatment phase using one of these treatments: Gemcitabine, sequential gemcitabine/docetaxel, Bacillus Calmette-Guerin (BCG), or Mitomycin C delivered directly into the bladder
  • (Phase 2 only) People of any gender who have been diagnosed with non-muscle invasive bladder cancer (stage Ta, Tis, or T1) and are in the ongoing maintenance phase of one of the eligible treatment programs
  • (Phase 1b only) People who are able to have a catheter inserted and who have been able to tolerate their first bladder treatment at an outpatient clinic
  • People who live within the area covered by the trial's supplier network
  • People whose home has access to Wi-Fi or mobile data to support virtual telehealth appointments
  • People aged 18 or older at the time of registration
  • People who have signed the informed consent form for the trial
  • People who are willing and able to follow the study protocol, as judged by the investigating doctor
  • People who are able to complete questionnaires on their own or with help from someone else
  • People who are willing to follow the required birth control guidelines (applicable to those who could potentially father or become pregnant)

Who may not be able to join:

  • People who are receiving any other investigational or standard treatment for bladder cancer that is not one of the eligible treatment regimens listed in this trial
  • People who are actively receiving treatment for any other cancer, except hormone therapy for breast or prostate cancer, or treatment for non-invasive skin cancer
  • People who require around-the-clock assistance with basic daily activities such as eating, bathing, or dressing
  • People who are currently admitted to a hospital (unless they are already enrolled in an Advanced Care at Home program)
  • People who have other serious illnesses or conditions that, in the investigating doctor's judgment, would make participation unsafe or affect the accurate assessment of the treatment
  • People with uncontrolled health conditions, including but not limited to: an active or ongoing infection, heart failure with symptoms, unstable chest pain, irregular heart rhythm, a heart attack within the past 6 months, a wound healing disorder, or a psychiatric or social situation that would make it difficult to follow the study requirements
  • People who are expected to need major surgery during the course of the trial
  • People who are known to have had an allergic reaction or intolerance to the drug regimens used in the trial
  • People who are pregnant or breastfeeding
  • People who have a known allergy or sensitivity to polysorbate 80 or paclitaxel (specific substances used in some medications)

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
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: Timothy D. Lyon, MD, Mayo Clinic

Phone: 855-776-0015

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
Registry
ClinicalTrials.gov
Start date
21 April 2025
Est. completion
31 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Incidence and severity of adverse events (AEs); Feasibility of in-home intravesical therapy

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