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The Safety Monitoring Committee Concluded Its Planned Safety Review For All Patients Treated With The INTASYL compound PH-762 In Phio Pharmaceuticals' Phase 1b Trial, No Serious Adverse Events Or Dose-limiting Toxicities Identified
Maximum Dose Concentration in Final Cohort Yields 85% Pathological Response (6 of 7 Patients); Complete Response (100% Tumor Clearance) in 4 of 6 Responders
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