The US Food and Drug Administration (FDA) is expected to make a Prescription Drug User Fee Act (PDUFA) decision by mid-2025.
US FDA accepts for review GSK’s Blenrep combinations for the treatment of relapsed/refractory multiple myeloma: London, UK Tuesday, November 26, 2024, 09:00 Hrs [IST] GSK plc an ...
The US Food and Drug Administration (FDA) has accepted for review a Biologics License Application (BLA) for belantamab ...
Pharma titan GSK has announced that US regulators have accepted for review Blenrep combinations for the treatment of relapsed ...
GlaxoSmithKline (GB:GSK) has released an update.Don't Miss our Black Friday Offers:Unlock your investing potential with TipRanks Premium - Now ...
The presumptive new CDC director, Dave Weldon, is a known vaccine safety skeptic. In contrast, the FDA choice — Johns Hopkins ...
Bioline RX Ltd Sponsored ADR ( (BLRX) ) has released its Q3 earnings. Here is a breakdown of the information Bioline RX Ltd Sponsored ADR ...
Acquisition supports Roche’s Pharma Strategy and allows for a range of potentially first and best-in-class therapies across ...
Former Wisconsin Rapids Lincoln baseball assistant Dan O'Connell recently lost an 18-year battle with leukemia. Here is how ...
BioLineRx (NASDAQ:BLRX – Free Report) had its target price trimmed by HC Wainwright from $21.00 to $9.00 in a report issued on Monday morning,Benzinga reports. The firm currently has a buy rating on ...
Poseida Therapeutics, Inc. (Nasdaq: PSTX) ("Poseida"), a clinical-stage allogeneic cell therapy and genetic medicines company ...
The Lehigh Valley Topper Cancer institute has announced that it is now offering treatment using autologous chimeric antigen ...