Technology Prognosis: Luxturna (Voretigene Neparvovec-rzyl)



Proposed Use Gene therapy for treatment of vision loss due to RPE65 gene mutation
Regulatory Status Phase I/II Trials Complete Phase III Trials in Progress Phase III Trials Published FDA Filing Complete FDA Approved
Estimated Commercial Availability Unable to Determine >2 years 1 to 2 years <6 months Currently Available

Check out this case study to see how we’ve saved a large hospital system millions of dollars.

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