Protara Therapeutics Inc.(TARA) announced updated results from its Phase 2 open-label ADVANCED-2 trial assessing intravesical TARA-002, the Company's investigational cell-based therapy, in high-risk Non-Muscle Invasive Bladder Cancer (NMIBC) patients with carcinoma in situ, or CIS (Ta/T1), who are Bacillus Calmette-Gurin (BCG)-Unresponsive
or BCG-Nave.
According to the company, TARA-002 has shown remarkable efficacy, achieving a 100% complete response rate at any time and a 67% 12-month landmark complete response rate in BCG-unresponsive patients. Additionally, it demonstrated a 76% complete response rate at any time and a 43% 12-month landmark complete response rate in BCG-naïve patients. The treatment also boasts a favorable safety and tolerability profile, with no reported Grade 3 or higher treatment-related adverse events.
The company continues to expect to present an interim update with results from about 25 six-month evaluable BCG-Unresponsive patients by the end of 2025.
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