Health Canada clears Pfizer cholesterol therapy
The approval is based on evidence available to date and reinforces the previous indication for reduction of cardiovascular events, such as myocardial infarction and stroke, in patients without
The US Food and Drug Administration (FDA) has granted accelerated approval to Bristol Myers Squibb’s (BMS) Zenbexus (iberdomide), along with daratumumab and hyaluronidase-fihj and dexamethasone (ZDd), to treat adult multiple myeloma (MM) patients.
The study results indicate bioequivalent pharmacokinetics between ANX-514 and the FDA-approved version of Taxotere. Furthermore, ANX-514, administered intravenously, did not cause hypersensitivity reactions in this study, as opposed