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Clinical trial to evaluate the efficacy and safety of erdafitinib TAR-210 intravesical delivery system compared to intravesical chemotherapy monotherapy in patients with non-muscle-invasive bladder cancer.
THE MAIN OBJECTIVE OF THIS STUDY IS TO COMPARE PROGRESSION-FREE DISEASE (PFS) BETWEEN PATIENTS RECEIVING ART-210 AND INTRAVESICAL CHEMOTHERAPY OF THE INVESTIGATOR'S CHOICE.
Technical Summary
- PHASE III RANDOMIZED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ERDAFITINIB TAR-210 INTRAVESICAL DELIVERY SYSTEM COMPARED TO INTRAVESICAL CHEMOTHERAPY MONOTHERAPY IN PATIENTS WITH INTERMEDIATE-RISK NON-MUSCLE-INVASIVE BLADDER CANCER (IR-NMIBC) AND SENSITIVE FGFR ALTERATIONS
- Code EudraCT: 2023-507684-19
- Protocol number: 42756493BLC3004
- Promoter: Janssen Research & Development
* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.
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