• Pfizer, PTC Therapeutics International, Roche, Sarepta Therapeutics, Solid Biosciences, Summit Therapeutics plc, and Wave Life Sciences are sponsoring Project HERCULES, which will generate and share critical disease level data across an entire condition
  • New approach has the potential to improve the chances of medicines for rare and orphan diseases receiving positive decisions from NICE and other pricing watchdogs

For the first time, pharmaceutical companies are sponsoring a project, led by Duchenne UK, to generate, align and share disease-level data across an entire condition for health technology assessments (HTA). The collaboration, known as HERCULES, will focus on medicines for Duchenne muscular dystrophy.

The HERCULES industry partners announced today are:

  • Pfizer Inc
  • PTC Therapeutics International Ltd
  • Roche
  • Sarepta Therapeutics, Inc
  • Solid Biosciences
  • Summit Therapeutics Plc
  • Wave Life Sciences USA, Inc

The unique initiative, launched by the Duchenne muscular dystrophy research charity Duchenne UK, aims to radically simplify the way evidence is generated for submissions to HTA bodies, such as the National Institute for Health and Care Excellence (NICE) and the Haute Autorité de Santé (HAS). The University of Leicester and University of Sheffield have also partnered on HERCULES in the development of a quality of life metric and data analysis. 

While this new initiative focuses on Duchenne muscular dystrophy, it paves the way for similar approaches in other rare diseases, and has the potential to better demonstrate the value of medicines for rare and orphan diseases. It is hoped that greater certainty over the value of these medicines could help to improve their chances of receiving positive HTA decisions.

Rare conditions affect around 3.5 million people in the UK[1] and 30 million people across Europe[2]. Yet only 5 per cent of rare diseases have a licensed treatment option in the UK[3]. Small patient populations and limited resources to build a robust evidence base are key hurdles in developing treatments for rare diseases. These obstacles tend to hinder the HTA approval of potentially life-changing treatments for rare diseases and their subsequent availability to NHS patients, even for medicines that have received regulatory approval.

Emily Crossley, Co-CEO of Duchenne UK, said: “As a parent of a child with Duchenne, it can be heartbreaking to know that access to life-changing treatments might be delayed because the assessment bodies don’t have the right evidence to make a decision. By pooling evidence through HERCULES, all partners involved can avoid ‘reinventing the wheel’ by producing evidence for similar submissions.

“We’re delighted that our industry partners have joined us to lead the way in this collaborative approach. HERCULES has the potential to transform health technology assessment submissions in Duchenne muscular dystrophy and other rare diseases. This could not only help industry and assessment bodies such as a NICE, but ultimately ensure that new treatments for DMD get to the boys who need them the most.”

Fleur Chandler, Future Pipeline Head, VEO at GSK R&D and a member of Duchenne UK’s Patient Advisory Board added: “With HERCULES, we have a patient organisation taking the lead to solve a problem that the industry has talked about for a long time, but where limited progress has been made to date. HERCULES gives us the opportunity to develop a much more robust evidence base for Duchenne muscular dystrophy. Some companies can dedicate considerable time and resource to developing the economic modelling and quality of life measures for their submissions. However, this is not the case for all, which runs the risk of uncertainty in decision making and, ultimately, patients losing out.”

Janis Clayton, General Manager at PTC Therapeutics Ltd, said: “HERCULES, led by Duchenne UK, provides an excellent opportunity for innovation and collaboration, bringing together as it does patient organisations, industry and academia. PTC are very pleased to be supporting, and actively involved in, this appropriately ambitious project.”

Duchenne UK would like to thank CMS Cameron McKenna Nabarro Olswang LLP for their legal support and advice on Project Hercules.

 - ENDS -

[1] Rare Diseases UK, What is a rare disease? Available at: http://www.raredisease.org.uk/what-is-a-rare-disease/, accessed: November 2017

[2] Eurordis, What is a rare disease? Available at: https://www.eurordis.org/sites/default/files/publications/Fact_Sheet_RD.pdf, accessed: January 2018

[3] Orphan Europe, Orphan Drugs. Available at: http://www.orphan-europe.com/about-us/orphan-drugs,  accessed: November 2017

Contact for more information and interview requests:

Molly Hunt, Communications Manager: [email protected], +44 (0)203 096 7496

 

NOTES TO EDITORS

 

About HERCULES

HERCULES will help produce a comprehensive, standardised evidence base for new treatments that have the potential to change the lives of patients with DMD. Led by Duchenne UK with seven pharmaceutical industry sponsors and two academic partners, the project will enable a stronger evidence base for new therapies for Duchenne Muscular Dystrophy (DMD) required by regulatory bodies, such as the National Institute for Health and Care Excellence (NICE). These evidence requirements are very different from the evidence required to grant regulatory approval for a medicine.

 

Phase One of HERCULES will begin in early 2018, and focus on understanding the current evidence base, the cost of DMD and lives lost to it, as well as current measures of success in DMD clinical trials. This unique project with seven industry sponsors will enable development of the critical components required for a successful HTA submission including:

  • A critique of current Quality of Life metrics and bespoke DMD metric
  • Data analysis to map clinical trial endpoints and natural history data to clinical outcomes
  • A burden of illness study
  • A core economic model which companies can tailor to their own needs

 

Phase Two will be announced in the second half of 2018.

 

About Duchenne Muscular Dystrophy (DMD)

  • There are around 2,500 boys affected by DMD in the UK and around 300,000 worldwide. It is classified as a rare disease
  • DMD is the most common fatal genetic disease diagnosed in childhood, almost exclusively affecting boys
  • Children born with DMD cannot produce the protein dystrophin which is vital for muscle strength and function. Muscle weakness starts in early childhood. Many use a wheelchair by around the age of 12. As deterioration continues it leads to paralysis and early death, often in their 20s. There is no treatment or cure

 

About Duchenne UK

  • Duchenne UK is a lean, ambitious and highly focused charity with a clear vision: to fund and accelerate treatments and a cure for DMD. Duchenne UK has raised more than £5.5million in five years, and spent or committed £5million to DMD research projects – more than any other organisation
  • Duchenne UK is leading the drive towards the efficient repurposing of existing medicines to bring new treatments for DMD
  • Duchenne UK believes that every child with Duchenne should be given the opportunity to access a clinical trial. Duchenne UK created the DMD Hub in 2016 to expand and develop the infrastructure for DMD trials in the UK and accelerate access to clinical studies for those who are interested in participating
  • The charity has been formed by the coming together of Joining Jack and Duchenne Children's Trust, the two biggest funders of research in the UK in the last three years. Its president is HRH The Duchess of Cornwall. Its patrons include the broadcasters Krishnan Guru-Murthy and Mary Nightingale, and the sports stars Owen Farrell, Kris Radlinski and Andy Farrell

Visit duchenneuk.org for more information or follow @DuchenneUK on Twitter.