• Theralase has launched new clinical study sites in the U.S. and Canada for its Phase II trial of Ruvidar™ in BCG-unresponsive NMIBC.
• Phase II data shows a 61.9% complete response rate among patients, with 43.6% maintaining this response for at least 12 months.
• The treatment has demonstrated a strong safety profile, with 100% of patients experiencing no serious adverse events related to the therapy.
• Theralase is actively seeking partnerships for the international commercialization of Ruvidar™, with regulatory approval targeted for 2026.