Efficacy and Safety of Intravesical TARA-002 Compared With Investigator's Choice of Intravesical Chemotherapy in Participants With BCG-naïve High-grade Non-muscle Invasive Bladder Cancer
Sponsor: Protara Therapeutics
ClinicalTrials ID:NCT07480356
This trial evaluates TARA-002's efficacy and safety in treating high-grade NMIBC in BCG-naïve adults. Eligible participants must be 18+, with confirmed high-grade non-muscle invasive CIS. TARA-002 involves 6 weekly instillations, with maintenance or reinduction based on response. The comparator is investigator-chosen intravesical chemotherapy, also administered in a structured regimen.
Patient Parameters
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Program Overview
The goal of this clinical trial is to learn if TARA-002 can treat high-grade non-muscle invasive bladder cancer (NMIBC) in BCG-naïve adults 18 years of age or older.
The main questions it aims to answer are:
- Can the study drug help participants with this type of cancer?
- Is the study drug safe?
- What are the side effects of the study drug?
Researchers will compare TARA-002 to chemotherapy to see if TARA-002 works to treat NMIBC.
Eligibility Criteria
Inclusion Criteria
- Male or female participants 18 years of age or older at the time of signing informed consent
- Participants who have voluntarily given written informed consent after the nature of the study has been explained according to applicable requirements prior to study entry
- Central histologic confirmation of high-grade non-muscle invasive CIS (± Ta/T1) with active disease
- Participants who are BCG naive, or participants who are BCG exposed and have not received intravesical BCG for at least 24 months prior to the most recent CIS diagnosis, or participants who received ≤2 doses of BCG within the 24 months prior to the most recent CIS diagnosis
Exclusion Criteria
- Penicillin allergy (participants with a questionable history of allergy to penicillin will undergo penicillin blood allergy testing via central laboratory
- Central confirmed variant histology
- Concomitant prostatic or upper tract urothelial involvement per Investigator's assessment
- Nodal and metastatic disease are excluded if they existed at any time (whether present or in the past)
- Any history of ≥ T2 bladder cancer that existed at any point in time in the participant's history
For more information on eligibility criteria, please contact the Sponsor.
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| East Valley Urology Center of Arizona | 85140 | Queen Creek | Arizona |
| Arkansas Urology | 72211 | Little Rock | Arkansas |
| Michael Oefelein Clinical Trials | 93301 | Bakersfield | California |
| Renown Regional Medical Center | 63110 | St Louis | Missouri |
| START - Carolinas | 29572 | Myrtle Beach | South Carolina |
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