The US Food and Drug Administration (FDA) is expected to make a Prescription Drug User Fee Act (PDUFA) decision by mid-2025.
A treatment approach harnessing bispecific antibodies to target cancerous cells unlocks new possibilities for patients, says ...
The study compared CARVYKTI's efficacy and safety against standard-of-care regimens in patients with multiple myeloma.
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 ...
Cesar Rodriguez, MD, discussed several key aspects of talquetamab use in the treatment of relapsed/refractory multiple ...
GSK plc (GSK, GSK.L) announced that the US Food and Drug Administration has accepted for review a Biologics License Application (BLA) ...
The American Journal of Managed Care provides insights into the latest news and research in managed care across multimedia ...
Santhosh K. Sadashiv, MD, discusses the role of chimeric antigen receptor T-cell therapy in patients with multiple myeloma.
The American Journal of Managed Care provides insights into the latest news and research in managed care across multimedia platforms.
A ground breaking study mapping the immune microenvironment in Multiple Myeloma identifies critical immune changes and ...
GlaxoSmithKline (GB:GSK) has released an update.Don't Miss our Black Friday Offers:Unlock your investing potential with TipRanks Premium - Now ...