TARA-002 demonstrates 72% complete response rate at any time, 67% complete response rate at the 6-month landmark and 55% complete response rate at the 12-month landmark in BCG-Naïve patients
Favorable safety and tolerability profile with no Grade 3 or greater treatment-related adverse events
Company remains on track to initiate the ADVANCED-3 registrational trial in BCG-Naïve patients in 2H 2026
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