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Protara Therapeutics Announces Updated Interim Data from Phase 2 ADVANCED-2 Trial of TARA-002 in BCG-Naïve NMIBC Patients

TARA-002 demonstrates 72% complete response rate at any time in BCG-Naïve patientsTARA-002 demonstrates a 69% complete response rate at the 6-month landmark and a 50% complete response rate at the 12-month landmark in BCG-Naïve patientsFavorable safety and tolerability profile observed with no Grade 3 or greater treatment-related adverse events reportedCompany obtained written feedback from FDA on registrational path forward for TARA-002 in BCG-Naïve patientsCompany remains on track to report in

articleProtara Therapeutics, Inc.December 3, 20259/company/protara-therapeutics-inc/news/protara-therapeutics-announces-updated-interim-130000153
Protara Therapeutics Announces Updated Interim Data from Phase 2 ADVANCED-2 Trial of TARA-002 in BCG-Naïve NMIBC Patients

About this update from Protara Therapeutics, Inc.

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More updates from Protara Therapeutics, Inc.

Protara Therapeutics, Inc.carcinoma in situBCGbladder cancerBacillus Calmette-GuérinProtaraCISProtara TherapeuticsThe CompanyNMIBCFood and Drug AdministrationInterim Results