We are delighted to announce that the MHRA have decided to maintain a positive opinion on the Early Access to Medicines Scheme for Raxone to treat people living with Duchenne muscular dystrophy. This means that Raxone remains on course to have its EAMS award renewed, so that patients over 10 years of age, showing a decline in respiratory function and who are currently not taking glucocorticoid steroids, can continue to access Raxone until June 2019.

This was a joint effort from the entire Duchenne community and Action DuchenneDMD PathfindersDuchenne Family Support GroupDuchenne UK and Muscular Dystrophy UK cannot thank enough, all of you who provided vital feedback to this process.

Each and every organisation appreciates how much effort and courage goes into providing this testimony, whether it is delivered in writing or in person, and we have no doubt this had a positive impact on the committee’s decision.

The UK Commission on Human Medicines (CHM) determined from the evidence and testimony received, that the risk/benefit profile was acceptable and there is a clear high unmet medical need for patients with Duchenne. Receiving feedback from such a wide spectrum of the community was integral to this.

Kaye Hemming's 23 year old son, Dominic, is awaiting Raxone from Queens Square, she said:

'To say that I am pleased with the decision made by MHRA would be a huge understatement. They listened to myself, other parents and people living with DMD and now hopefully my son and others waiting for Raxone will get is dispensed very shortly. I can't emphasis how important this drug is. Any treatment that potentially could increase respiratory function of a patient with a life limited illness is a godsend. Brilliant decision."

The Early Access to Medicines Scheme (EAMS) for Raxone

  • The aim of the EAMS is to provide earlier availability of promising medicines to patients in the UK where there is high unmet clinical need.
  • It is to slow the decline of respiratory function in patients with Duchenne from the age of 10 years who are currently not taking glucocorticoids.
  • At the same time more data is able to be captured, to evaluate the effectiveness of the medicine.
  • Treatment will only be provided in specialist centres that are experienced in managing Duchenne and there is the requirement for careful monitoring to ensure the safety of patients during the EAMS.
  • People with Duchenne may discuss together with their doctor whether they are suitable for this treatment.

This Frequently Asked Questions document provides more detail.