Ph. 1b patients #5 and #6 still cancer free after 2 years24-months (2y or 730 days) cancer free:
MD&A of Nov. 29, 2021:
Theralase®’s Study successfully achieved the primary objective of safety and tolerability, secondary objective of pharmacokinetics and exploratory objective of efficacy. The Study results demonstrated a strong efficacy signal with a 67% Complete Response (“CR”) rate in the Therapeutic Dose group (0.70 mg/cm2 ) after only a single Study treatment, with patients five and six demonstrating a Complete Response (“CR”) (indicated by negative cystoscopy and negative urine cytology) with no presence, recurrence or progression of the disease at up to 24 months post treatment.
MD&A of April 29, 2022:
Theralase®’s Study successfully achieved the primary objective of safety and tolerability, secondary objective of pharmacokinetics and exploratory objective of efficacy. The Study results demonstrated a strong efficacy signal with a 67% Complete Response (“CR”) rate in the Therapeutic Dose group (0.70 mg/cm2 ) after only a single Study treatment, with patients five and six demonstrating a Complete Response (“CR”) (indicated by negative cystoscopy and negative urine cytology) with no presence, recurrence or progression of the disease at up to 24 months post treatment.
MD&A of May 30, 2022:
Theralase®’s Study successfully achieved the primary objective of safety and tolerability, secondary objective of pharmacokinetics and exploratory objective of efficacy. The Study results demonstrated a strong efficacy signal with a 67% Complete Response (“CR”) rate in the Therapeutic Dose group (0.70 mg/cm2 ) after only a single Study treatment, with patients five and six demonstrating a Complete Response (“CR”) (indicated by negative cystoscopy and negative urine cytology) with no presence, recurrence or progression of the disease at up to 24 months post treatment.