Novartis Luxturna®, a novel gene therapy treatment for rare inherited eye disorder, has been recommended by NICE for use on the NHS.
The draft highly-specialised technologies guidance recommends voretigene neparvovec (also called Luxturna and made by Novartis Pharmaceuticals UK) for people with vision loss caused by inherited retinal dystrophy from confirmed RPE65 gene mutations and who have enough viable retinal cells.
Voretigene neparvovec is the first licensed gene therapy for vision loss caused by RPE65-mediated inherited retinal dystrophy.
Inherited retinal dystrophies are a group of eye diseases caused by gene mutations which result in the gradual degeneration of the light sensitive cells (photoreceptor cells) on the back of the eye.
The RPE65 gene provides instructions for making a protein that is essential for normal vision. RPE65-mediated inherited retinal dystrophies are rare and serious. Usually diagnosed in childhood, they involve progressive loss of vision which ultimately leads to near-total blindness and severely affects the quality of life of people with the condition, their families and carers. Current treatment is supportive care, such as the use of low-vision aids.
The voretigene neparvovec evaluation at NICE has taken 20 weeks instead of the average of 38 weeks within the Highly Specialised Technologies programme.
Voretigene neparvovec is a gene therapy injected directly into the retina by a surgeon. It works by introducing a healthy copy of the defective RPE65 gene into the retinal cells, enabling people with the condition to produce functional RPE65 protein.
Evidence from clinical trials shows that, in the short term, voretigene neparvovec improves vision and prevents the condition from getting worse. There is no long-term clinical evidence, but the committee considered it is biologically plausible that the treatment effect is likely to continue for decades.
The exact number of people living with the condition is uncertain. The company estimates that 86 people would be eligible for treatment with voretigene neparvovec in England.
Voretigene neparvovec is being recommended for people with inherited retinal dystrophies, after the company worked with NHS England to reach a commercial arrangement which ensured the technology did not breach the Budget Impact Test.
Voretigene neparvovec is the second innovative gene therapy which NICE has produced positive guidance on in its highly specialised technology programme – after Strimvelis for treating adenosine deaminase deficiency–severe combined immunodeficiency was recommended in February 2018.
The list price of voretigene neparvovec is £613,410 per patient. This technology breached the Budget Impact Test, meaning it would have cost the NHS more than £20 million in one of the first three years after being introduced. However, the company has a commercial arrangement with NHS England making the treatment available to the NHS at a discount, the size of which is commercial in confidence.
The draft guidance is now with consultees, including the company, healthcare professionals and patient/carer organisations who have the opportunity to appeal against the draft recommendations. If no appeals are received NICE expects to publish final guidance next month.
Meindert Boysen, Director of the Centre for Health Technology Evaluation at NICE, said: “This is a highly innovative treatment for a very distressing, inherited condition so we are pleased the company has worked with us and NHS England and Improvement to allow us to offer these families hope for the future.
“The company’s willingness to work with us early and constructively has allowed us to publish this guidance on a much faster timeline than normal which is good news for patients.”
“We are delighted with today’s decision by NICE to recommend voretigene neparvovec for use in patients with vision loss due to a genetic mutation in both copies of the RPE65 gene” said Haseeb Ahmad, Country President of Novartis UK and Managing Director (UK, Ireland and Nordics) of Novartis Pharmaceuticals. “Through effective collaboration with NICE and NHS England, it has been possible to secure rapid access to the first and only one-time gene therapy for patients living with this condition.”