Japan allows Takeda to change CPP drug dosage
According to the latest move, the maximum allowable dosage of the drug for CPP changes from 90µg/kg/4 weeks to 180µg/kg/4 weeks. The Committee on Drug I, Pharmaceutical Affairs
The US Food and Drug Administration (FDA) has granted breakthrough therapy designation to Eli Lilly and Company’s (Lilly) olomorasib as a potential treatment for adults with advanced pancreatic cancer who have already received at least one prior systemic therapy.