The Medical Letter n.23 / 2020
Nr. 23 del 01/12/2020TML n. 23/2020 TEMPISTICHE DI SOMMINISTRAZIONE DEL REMDESIVIR NELLA COVID-19
Il remdesivir (Veklury-Gilead Sciences), un farmaco antivirale in fase sperimentale somministrato tramite infusione EV, è ora disponibile negli Stati Uniti grazie a un’autorizzazione all’uso in...
TML n. 23/2020 UNA NUOVA INSULINA LISPRO PER IL DIABETE
La US Food and Drug Administration (FDA) ha approvato l’insulina lispro-aabc (Lyumjev-Eli Lilly; il farmaco ha ottenuto l’autorizzazione all’immissione in commercio da parte dell’EMA tramite...
TML n. 23/2020 CAPLACIZUMAB PER L’iTTP
La US Food and Drug Administration (FDA) ha approvato il caplacizumab-yhdp (Cablivi-Sanofi), un frammento anticorpale diretto contro il fattore di von Willebrand, per l’uso in associazione a...
TML n. 23/2020 APOMORFINA PER VIA SUBLINGUALE PER LA MALATTIA DI PARKINSON
La US Food and Drug Administration (FDA) ha approvato una formulazione sublinguale sotto forma di pellicola dell’agonista dopaminergico non ergolinico apomorfina (Kynmobi-Sunovion negli USA; non...
TML n. 23/2020 VILTOLARSEN PER LA DISTROFIA MUSCOLARE DI DUCHENNE
L’oligonucleotide antisenso viltolarsen (Viltepso-NS Pharma negli USA; il farmaco ha ricevuto la designazione di farmaco orfano dalla Commissione Europea in data 4 giugno 2020; non disponibile in...
TML n. 23/2020 DUE NUOVI DOSAGGI DI DULAGLUTIDE PER IL DIABETE
La US Food and Drug Administration (FDA) ha approvato due nuovi dosaggi (3 mg e 4,5 mg) dell’agonista del recettore del peptide-1 glucagone-simile (GLP-1) dulaglutide (Trulicity-Eli Lilly) per il...
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