FDA genehmigt Utebzi zur Behandlung komplizierter Harnwegsinfektionen einschließlich Pyelonephritis
Tebipenem pivoxil wird das erste in den USA zugelassene orale Carbapenem und bietet eine nicht-intravenöse Option bei schweren Harnwegsinfektionen.
31 Artikel
Tebipenem pivoxil wird das erste in den USA zugelassene orale Carbapenem und bietet eine nicht-intravenöse Option bei schweren Harnwegsinfektionen.
Myqorzo (aficamten) erhält FDA-Zulassung für symptomatische obstruktive HCM und bietet Patienten eine neuartige Therapieoption mit einem kardialen Myosin-Inhibitor.
Wellcovorin becomes the first approved treatment for cerebral folate deficiency tied to FOLR1 gene variants, offering hope for a rare neurological condition.
Nivolumab plus standard chemotherapy receives FDA approval for classical Hodgkin lymphoma, expanding immunotherapy's role in blood cancers.
MSK-led research drove 10 FDA cancer drug approvals in 2025, including nivolumab combined with chemotherapy for classical Hodgkin lymphoma.
Nivolumab added to standard chemotherapy wins FDA approval, offering a new frontline option for classical Hodgkin lymphoma patients.
Sevabertinib and zongertinib win FDA approval for HER2-mutant NSCLC, expanding targeted therapy options for previously treated patients.
Inqovi gains approval for newly diagnosed AML in patients 75+ or with comorbidities, offering a gentler oral treatment route.
Baxdrostat becomes the first-in-class aldosterone synthase inhibitor approved to treat resistant hypertension alongside existing drugs.
Memorial Sloan Kettering-led trials produced 11 new FDA-approved cancer therapies in a single year, spanning multiple tumor types.
Sonrotoclax (Beqalzi), a next-gen BCL-2 inhibitor, wins accelerated FDA approval for relapsed or refractory MCL after BTK inhibitor failure.
The FDA approved zenocutuzumab-zbco for adults with advanced, unresectable, or metastatic cholangiocarcinoma, a rare and aggressive bile duct cancer with limited treatment options.