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La FDA Approva Utebzi per le Infezioni Complicate delle Vie Urinarie, Inclusa la Pielonefrite
Metabolic Health

La FDA Approva Utebzi per le Infezioni Complicate delle Vie Urinarie, Inclusa la Pielonefrite

Il tebipenem pivoxil diventa il primo carbapeneme orale approvato negli Stati Uniti, offrendo un'opzione non endovenosa per le infezioni urinarie gravi.

Approvazione farmaco
21 giu 2026 0
FDA Approva l'Aficamten per la Cardiomiopatia Ipertrofica Ostruttiva
Heart Health

FDA Approva l'Aficamten per la Cardiomiopatia Ipertrofica Ostruttiva

Myqorzo (aficamten) ottiene l'approvazione FDA per la cardiomiopatia ipertrofica ostruttiva sintomatica, offrendo una nuova opzione di inibitore della miosina cardiaca per i pazienti.

Approvazione farmaco
14 giu 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.

Approvazione farmaco
31 mag 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.

Approvazione farmaco
27 mag 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.

Approvazione farmaco
26 mag 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.

Approvazione farmaco
26 mag 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.

Approvazione farmaco
24 mag 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.

Approvazione farmaco
22 mag 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.

Approvazione farmaco
19 mag 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.

Approvazione farmaco
19 mag 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.

Approvazione farmaco
15 mag 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.

Approvazione farmaco
13 mag 2026 0
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