”Patients with advanced HCC, who have progressed on at least one prior line of treatment, is a difficult-to-treat population. Achieving durable clinical benefit for the majority of the patients with a good safety and tolerability profile, enables patients to benefit from the combination treatment longer. It provides us with added confidence in accelerating the fostrox development program and we look forward to engaging further with FDA to discuss final study design of the planned, registrational phase 2b study with accelerated approval intent,” says Dr. Pia Baumann, CMO at Medivir.
