Biothera anticancer drug shows safety in trial
The single-dose, dose-escalating phase I study examined the safety and tolerability of a single injection of the drug in 24 healthy volunteers. Biothera plans to initiate a multiple-dose,
The US Food and Drug Administration (FDA) has approved two Jazz Pharmaceuticals regimens containing Ziihera (zanidatamab-hrii) for the first-line treatment of adults with unresectable, locally advanced or metastatic human epidermal growth factor receptor 2 (HER2)-positive gastroesophageal adenocarcinoma (GEA).