Oculis’ Privosegtor wins FDA breakthrough therapy status for Optic Neuritis
The FDA designation follows visual-function results from the Phase 2 ACUITY trial
The FDA designation follows visual-function results from the Phase 2 ACUITY trial
Applications include detailed scientific rationale and supporting clinical evidence
Under the agreement, AVT06 is licensed to enter the US market in the fourth quarter of 2026
Ranibizumab is a recombinant humanized IgG1 monoclonal antibody fragment that binds to and inhibits vascular endothelial growth factor A
Seeing well-controlled Phase 3 data that shows a marked slowing of lesion growth in Stargardt disease is deeply encouraging
ADX-248, which replaces ADX-743, is being developed for the treatment of metabolic inflammation, including obesity and hypertriglyceridemia
Vamikibart is the first targeted, non-steroid treatment designed to address the underlying inflammation driving UME
The study further confirmed that GAL-101 effectively crosses the blood-brain barrier
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