Novartis announced that the European Commission has approved Farydak (panobinostat, previously known as LBH589) capsules, in combination with bortezomib and...
This article summarizes the scientific review of the application leading to regulatory approval in the European Union.
Novartis has presented results from a pivotal Phase III clinical trial exploratory subgroup analysis showing a 7.8-month improvement in median...
The National Institute for Health and Care Excellence (NICE) in a final appraisal now recommends Farydak + Velcade (panobinostat +...
Novartis announced that the FDA has approved Farydak (panobinostat, previously known as LBH 589) capsules in combination with bortezomib and...
The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion for...
Novartis presented results from a pivotal Phase III trial showing a 37% improvement in progression-free survival (PFS) when using the...
Novartis has announced that the FDA Oncologic Drugs Advisory Committee (ODAC) did not recommend the investigational compound LBH 589 (panobinostat),...
Novartis has announced that results of a Phase III trial of the investigational compound LBH 589 (panobinostat) in combination with...
Purpose: Oral melphalan and dexamethasone (MDex) were considered a standard of care in light-chain (AL) amyloidosis. In the past decade, bortezomib has been increasingly used in combination with alkylating agents and dexamethasone. We prospectively compared the efficacy and safety of MDex and MDex with the addition of bortezomib (BMDex).