Safety and Toxicity Study of Intravesical Instillation of TARA-002 in Adults with High-grade Non-muscle Invasive Bladder Cancer (Phase 1a)

Completed · Phase 1

Conditions studied: Non-muscle Invasive Bladder Cancer

In brief

This study is an open-label dose escalation study (Phase 1a) to investigate the safety and toxicity of intravesical treatment of high-grade NMIBC (HGTa or CIS, including CIS with concomitant Ta) after transurethral resection of bladder tumor (TURBT) and/or biopsy using TARA-002 in adults unable to obtain intravesical Bacillus Calmette-Guérin (BCG), adults who have received at least one dose of intravesical BCG or adults who have received at least one dose of intravesical chemotherapy. Dosing will start in subjects with HGTa or CIS (including CIS with concomitant Ta), and all subjects will receive 6 weeks of treatment at a fixed volume with varying dose levels.

Key facts

Study ID

NCT05085977

Run by

Protara Therapeutics

People needed

12

Starts

2022-03-10

Expected to finish

2024-10-30

Last updated by the study team

2025-01-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female subjects 18 years of age or older at the time of signing the informed consent
• Subjects who have voluntarily given written informed consent after the nature of the study has been explained according to applicable requirements prior to study entry
• Subjects with a histologically confirmed, high-grade Ta or CIS (including CIS with concomitant Ta) urothelial cell carcinoma of the bladder on central review
• Subjects who are treatment naïve, are unable to obtain intravesical BCG for the treatment of NMIBC, have received at least one dose of intravesical BCG, or at least one dose of intravesical chemotherapy

You may not qualify if…

• Penicillin allergy (subjects with a questionable history of allergy to penicillin or no history of penicillin use will undergo penicillin blood allergy testing prior to inclusion in the study)
• Predominant (defined as > 50%) adenocarcinoma, squamous cell carcinoma, or histological variants including plasmacytoid, sarcomatoid, or squamous components according to central review
• Concomitant prostatic or upper tract urothelial involvement, per Investigator's assessment
• Nodal involvement or metastatic disease that existed at any time (past or present disease)
• Bladder cancer stage ≥ T1 within the last 36 months according to central histology review
• Bladder cancer stage CIS with concomitant T1
• For more information on eligibility criteria, please contact the sponsor.

Where it is running

• USC Norris Cancer Center — Los Angeles, California, United States
• Mayo Clinic — Jacksonville, Florida, United States
• Tulane Medical Center — New Orleans, Louisiana, United States
• Chesapeake Urology Research Associates — Baltimore, Maryland, United States
• Mayo Clinic — Rochester, Minnesota, United States
• New Jersey Urology — Mount Laurel, New Jersey, United States
• Premier Medical Group of the Hudson Valley — Poughkeepsie, New York, United States
• University of Rochester, Department of Urology — Rochester, New York, United States
• Carolina Urologic Research Center — Myrtle Beach, South Carolina, United States
• Urology Associates PC — Nashville, Tennessee, United States
• UT Health San Antonio — San Antonio, Texas, United States
• PMSI Republican Clinical Hospital "T. Mosneaga," ARENSIA Exploratory Medicine Phase I Unit — Chisinau, Moldova
• Spitalul Clinic de Nefrologie Carol Davila — Bucharest, Romania
• Arensia Kapitanivka — Kapitanivka, Ukraine

Full record on ClinicalTrials.gov

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