FDA rejects Akzo Nobel’s menopause drug
As a result, Akzo Nobel has decided not to launch the drug in the US and has accordingly withdrawn its application with the FDA. The decision by the
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).