$850K Price Tag For Blindness Drug Makes It One Of Most Expensive In World — But There’s A Twist
In a novel arrangement, drugmaker Spark Therapeutics will offer discounts based on whether or not the drug, Luxturna, works initially and remains effective.
The Associated Press:
Price Tag On Gene Therapy For Rare Form Of Blindness: $850K
A first-of-its kind genetic treatment for blindness will cost $850,000 per patient, making it one of the most expensive medicines in the world and raising questions about the affordability of a coming wave of similar gene-targeting therapies. The injectable treatment from Spark Therapeutics can improve the eyesight of patients with a rare genetic mutation that affects just a few thousand people in the U.S. Previously there has been no treatment for the condition, which eventually causes complete blindness by adulthood. (1/3)
The Washington Post:
Gene Therapy For Inherited Blindness Sets Precedent: $850,000 Price Tag
The drug, called Luxturna, is the realization of a long-sought scientific dream: The one-time treatment corrects a faulty gene to improve vision, allowing patients to see the stars or their parents' faces. Only 1,000 to 2,000 people in the United States are thought to have deteriorating vision caused by this errant gene, called RPE65, but Luxturna is widely expected to be the first in a wave of cutting-edge treatments that are targeted at fixing the causes of a wide range of genetic diseases — while also raising difficult questions about how to pay for them. (Johnson, 1/3)
The Wall Street Journal:
Drug Firm Spark Therapeutics Will Charge $850,000 For Vision-Loss Gene Therapy
To address concerns about the cost of the drug, Luxturna, Spark said it is offering alternative payment arrangements to health insurers, including partial refunds if a patient’s vision doesn’t improve significantly after treatment. The company also is seeking U.S. government clearance to allow insurers to spread out payments for Luxturna in installments. U.S. regulators approved Luxturna last month, making it the first therapy in the U.S. to deliver a functional gene to replace a faulty disease-causing one. (Loftus, 1/3)