Non-Muscle Invasive Bladder Neoplasms

6

Review clinical trials related to Non-Muscle Invasive Bladder Neoplasms. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Clinical Study of Intismeran Autogene (V940) and BCG in People With Bladder Cancer (V940-011/INTerpath-011)

Researchers are looking for new ways to treat people with high-risk non-muscle invasive bladder cancer (HR NMIBC). NMIBC is cancer in the tissue that lines the inside of the bladder but has not spread to the bladder muscle or outside of the bladder. High-risk means NMIBC may have a high chance of getting worse or coming back after treatment. HR NMIBC can also include carcinoma in situ (CIS). CIS is bladder cancer that appears flat and is only in the inner layer (surface) of the bladder. CIS is not raised and is not growing toward the center of the bladder. The standard treatment for HR NMIBC is a procedure to remove the tumor called transurethral resection of the bladder tumor (TURBT) followed by Bacillus Calmette-Guerin (BCG). Standard treatment is something that is considered the first line of treatment for a condition. BCG is an immunotherapy, which is a treatment that helps the immune system fight cancer. However, BCG may not work to treat HR NMIBC in some people. Researchers want to learn if adding intismeran autogene, the study treatment, to standard treatment can help treat HR NMIBC. Intismeran autogene is designed to help a person's immune system attack their specific cancer. The goal of this study are to learn if people who receive V940 with BCG live longer and without the cancer growing, spreading, or coming back compared to people who receive BCG alone.

Participants needed: 308
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Merck Sharp & Dohme LLCUpdated: Oct 1, 2026Locations: 89
Eligibility criteria

Has high-risk non-muscle invasive (HG Ta, T1, and/or CIS) UC of the bladder [+5]

Has a history of or concurrent locally-advanced (ie, T2, T3, T4) or metastatic U... [+10]

Status: Recruiting

A Study to Evaluate TAR-210 Versus Intravesical Chemotherapy Treatment in Participants With High Risk Non-Muscle-Invasive Bladder Cancer

The main purpose of this study is to compare the disease-free survival (the length of time after randomization that a participant survives without any signs or symptoms of the cancer returning, or progressing) between Bacillus Calmette-Guérin (BCG) treated participants receiving treatment with TAR-210 versus investigator's choice of intravesical chemotherapy for treatment of high-risk non-muscle-invasive bladder cancer (HR-NMIBC).

Participants needed: 220
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Janssen Research & Development, LLCUpdated: Sep 28, 2026Locations: 114
Eligibility criteria

Histologically confirmed diagnosis by local pathology of papillary-only HR-NMIBC... [+5]

Presence of CIS at any point from time of diagnosis of papillary-only HR-NMIBC r... [+4]

Status: Recruiting

A Study to Assess Real-World Use and Outcomes of TAR-200 for Participants With Non-Muscle Invasive Bladder Cancer (NMIBC) in the United States

The purpose of this study is to assess how well TAR-200 works in real-word by measuring the time taken from the first TAR-200 insertion to worsening of cancer or until the signs and symptoms of cancer occur again (disease-free survival) in participants with non-muscle invasive bladder cancer (NMIBC; an early-stage bladder cancer that is limited to the inner lining of bladder).

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Janssen Research & Development, LLCUpdated: Sep 25, 2026Locations: 19
Eligibility criteria

Has a confirmed diagnosis of NMIBC based on TURBT or cold cup biopsy [+3]

Has any medical condition deemed by the health care practitioner (HCP) as contra... [+4]

Status: Recruiting

A Study to Evaluate TAR-210 Versus Single Agent Intravesical Cancer Treatment in Participants With Bladder Cancer

The main purpose of this study is to compare the disease-free survival between participants receiving treatment with TAR-210 versus investigator's choice of intravesical chemotherapy for treatment of intermediate-risk NMIBC.

Participants needed: 641
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Janssen Research & Development, LLCUpdated: Sep 25, 2026Locations: 193
Eligibility criteria

Main study only: Have a histologically confirmed diagnosis (within 90 days of ra... [+6]

Known allergies, hypersensitivity, or intolerance to any study component or its... [+4]

Status: Not yet recruiting

Feasibility of HISA During TURBT for NMIBC

The goal of this prospective pilot study is to evaluate the safety and feasibility of using heated saline during bladder tumor surgery in patients with non-muscle invasive bladder cancer. The main questions it aims to answer are: Can heated saline be given during bladder tumor removal surgery safely? Does using heated saline keep the bladder tumor from coming back? Researchers will compare the heated saline to room temperature saline to see if the heated saline works to prevent the bladder tumor from coming back. Participants will: * Have heated saline or room temperature saline during bladder tumor surgery * Visit the clinic at 2 weeks, 3 and 6 months after bladder tumor surgery * Complete questionnaires about quality of their life and symptoms before and after surgery * Provide urine samples to test your urine at each visit before and after surgery * To have a cystoscopy to check your bladder for tumors

Participants needed: 40
Trial details
Age: 18-89Biological sex: AllType: InterventionalSponsor: CAMC Health SystemUpdated: Sep 14, 2026Locations: 1
Eligibility criteria

Male or female patients [+5]

Ages less than 18 years of age [+10]

Status: Recruiting

Study on the Occurrence of Possible Relapses and on the Quality of Life in Patients Who Underwent TURBK.

A database has been created and will be used in which data will be collected in electronic format relating to adult patients who underwent one of the following endoscopic resection surgeries: TURBK, MAPPING, TURBK SECOND LOOK, BLADDER BIOPSIES.

Participants needed: 20,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: IRCCS San RaffaeleUpdated: Dec 12, 2023Locations: 1
Eligibility criteria

18 years or older [+3]

Age <18 years [+1]