NICE recommends PTC Therapeutics Duchenne muscular dystrophy treatment

pharmafile | July 20, 2016 | News story | Research and Development, Sales and Marketing Duchenne Muscular Dystrophy, PTC Therapeutics 

PTC Therapeutics has announced that the National Institute for Health and Care Excellence has issued final guidance recommending Translarna (ataluren) for ambulatory patients aged five and over with nonsense mutation Duchenne muscular dystrophy in connection with a managed access agreement with NHS England.

A rare genetic disease, primarily affecting males, Duchenne muscular dystrophy is a progressive muscular disorder caused by the lack of functional dystrophin protein. Disease sufferers lose the ability to walk from as early as 10 years old, and may begin to experience to potentially fatal lung and heart complications in their late teens and early twenties.

While rejected by the FDA in the US, Translarna has been approved by the EMA. NICE had backed the drug in initial guidance, and this latest guidance will mean Duchenne patients can now access the first approved therapy to treat the underlying causes of the disease.

Paul Lenihan, CEO of Action Duchenne, says: “We are delighted that this positive recommendation from NICE has now been published. This is such an important day for the Duchenne community, which has been working hard to make this ground-breaking drug available to boys with nonsense mutation Duchenne muscular dystrophy.”

Janis Clayon, General Manager for UK and Ireland at PTC Therapeutics, comments: “Translarna is the first and only licensed treatment to address the underlying cause of Duchenne muscular dystrophy. I am very pleased that the completion of this important review process undertaken by NICE and NHS England now ensures that a much-needed therapy is available for the children and young adults with nonsense mutation DMD that meet the requirements for the MAA.”

Sean Murray

Related Content

FDA pre-meeting report raises concerns over Sarepta’s gene therapy for Duchenne muscular dystrophy

The US Food and Drug Administration (FDA) has released a report in preparation for its …

Roche building

Roche’s Evrysdi drug for SMA shown to significantly increase survival

Roche’s Evrysdi therapy for the treatment of children with type 1 spinal muscular atrophy (SMA) …

Roche building

Roche’s SMA treatment Evrysdi approved by European Commission

The European Commission has granted marketing authorisation to Roche and PTC Therapeutics’ Evrysdi, for the …

Latest content