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FDA genehmigt Utebzi zur Behandlung komplizierter Harnwegsinfektionen einschließlich Pyelonephritis
Metabolic Health

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.

Arzneimittelzulassung
21. Juni 2026 0
FDA genehmigt Aficamten für obstruktive hypertrophe Kardiomyopathie
Heart Health

FDA genehmigt Aficamten für obstruktive hypertrophe Kardiomyopathie

Myqorzo (aficamten) erhält FDA-Zulassung für symptomatische obstruktive HCM und bietet Patienten eine neuartige Therapieoption mit einem kardialen Myosin-Inhibitor.

Arzneimittelzulassung
14. Juni 2026 0
FDA Approves Leucovorin for Cerebral Folate Deficiency Caused by FOLR1 Variants
Brain Health

FDA Approves Leucovorin for Cerebral Folate Deficiency Caused by FOLR1 Variants

Wellcovorin becomes the first approved treatment for cerebral folate deficiency tied to FOLR1 gene variants, offering hope for a rare neurological condition.

Arzneimittelzulassung
31. Mai 2026 0
FDA Approves Nivolumab Combination Regimen for Classical Hodgkin Lymphoma
Cancer Research

FDA Approves Nivolumab Combination Regimen for Classical Hodgkin Lymphoma

Nivolumab plus standard chemotherapy receives FDA approval for classical Hodgkin lymphoma, expanding immunotherapy's role in blood cancers.

Arzneimittelzulassung
27. Mai 2026 0
Nivolumab Gets FDA Nod for Classical Hodgkin Lymphoma in 2025 Drug Approval Wave
Cancer Research

Nivolumab Gets FDA Nod for Classical Hodgkin Lymphoma in 2025 Drug Approval Wave

MSK-led research drove 10 FDA cancer drug approvals in 2025, including nivolumab combined with chemotherapy for classical Hodgkin lymphoma.

Arzneimittelzulassung
26. Mai 2026 0
FDA Approves Nivolumab Combo for Classical Hodgkin Lymphoma
Cancer Research

FDA Approves Nivolumab Combo for Classical Hodgkin Lymphoma

Nivolumab added to standard chemotherapy wins FDA approval, offering a new frontline option for classical Hodgkin lymphoma patients.

Arzneimittelzulassung
26. Mai 2026 0
FDA Approves Two New HER2-Targeted Lung Cancer Drugs in 2025
Cancer Research

FDA Approves Two New HER2-Targeted Lung Cancer Drugs in 2025

Sevabertinib and zongertinib win FDA approval for HER2-mutant NSCLC, expanding targeted therapy options for previously treated patients.

Arzneimittelzulassung
24. Mai 2026 0
FDA Approves Oral AML Therapy for Elderly Patients Unfit for Intensive Chemo
Cancer Research

FDA Approves Oral AML Therapy for Elderly Patients Unfit for Intensive Chemo

Inqovi gains approval for newly diagnosed AML in patients 75+ or with comorbidities, offering a gentler oral treatment route.

Arzneimittelzulassung
22. Mai 2026 0
FDA Approves Baxfendy, a New Aldosterone Synthase Inhibitor for Hypertension
Metabolic Health

FDA Approves Baxfendy, a New Aldosterone Synthase Inhibitor for Hypertension

Baxdrostat becomes the first-in-class aldosterone synthase inhibitor approved to treat resistant hypertension alongside existing drugs.

Arzneimittelzulassung
19. Mai 2026 0
MSK Research Drives 11 FDA Cancer Drug Approvals in 2025
Cancer Research

MSK Research Drives 11 FDA Cancer Drug Approvals in 2025

Memorial Sloan Kettering-led trials produced 11 new FDA-approved cancer therapies in a single year, spanning multiple tumor types.

Arzneimittelzulassung
19. Mai 2026 0
FDA Approves Sonrotoclax for Hard-to-Treat Mantle Cell Lymphoma
Cancer Research

FDA Approves Sonrotoclax for Hard-to-Treat Mantle Cell Lymphoma

Sonrotoclax (Beqalzi), a next-gen BCL-2 inhibitor, wins accelerated FDA approval for relapsed or refractory MCL after BTK inhibitor failure.

Arzneimittelzulassung
15. Mai 2026 0
FDA Approves Zenocutuzumab-zbco for Advanced Cholangiocarcinoma
Cancer Research

FDA Approves Zenocutuzumab-zbco for Advanced Cholangiocarcinoma

The FDA approved zenocutuzumab-zbco for adults with advanced, unresectable, or metastatic cholangiocarcinoma, a rare and aggressive bile duct cancer with limited treatment options.

Arzneimittelzulassung
13. Mai 2026 0
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