Takeda seeks EMA approval for type-II variation of Rienso broad IDA indication
The approval will allow the use of Rienso in all adult iron deficiency anemia patients who cannot take oral iron, in addition to current indication for the treatment
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.
Pharmavite chief operating officer Mark Walsh said, "At 330,000 square feet, the Opelika-based Pharmavite facility is one of the largest vitamin, mineral and supplement (VMS) manufacturing facilities built