The USA-based Institute for Clinical and Economic Review (ICER) on Wednesday released a Final Evidence Report and Report-at-a-Glance on Luxturna (voretigene neparvovec; VN) for the treatment of vision loss associated with RPE65-mediated retinal disease.
US biotech firm Spark Therapeutics’ (Nasdaq: ONCE) gained US approval for Luxturna in December 2017, making it the first treatment for this condition, but also raising significant concerns about its extremely high price.
Spark set the price of Luxturna at $425,000 per eye or $850,000 for both, which was however below the $500,000 per eye that observers had been predicting. Actual payment has been linked to short- and long-term performance of the therapy
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