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Duchenne UK launches Project HERCULES to help patients get faster access to potentially life-changing treatments

2.9 from 17 votes
Monday, January 29, 2018

Duchenne UK is delighted to announce that seven leading pharmaceutical companies developing treatments for Duchenne Muscular Dystrophy, are collaborating with the charity on Project HERCULES, to develop a robust and relevant evidence base for payers to accelerate the time it takes for payers to make decisions about which medicines to fund. Duchenne UK is investing £200,000 in the initial stages of the project.

Project HERCULES aims to provide a core central evidence base to provide high quality material to enable an informed HTA process and enable smoother and speedier payer reviews for innovative treatments in Duchenne muscular dystrophy (DMD). The project will allow pharmaceutical companies to work together to build the evidence base for new therapies required by pricing watchdogs, such as the National Institute of Health and Care Excellence (NICE).

With a wave of treatments in, or about to enter clinical trials, and with some already gaining approval, the aim of HERCULES is to address the next challenge after medicines reach regulatory approval; how we get governments and health services to pay for these medicines.

It is widely recognised that the pace of innovation in treatments and medicines is outstripping the time it takes to approve them for use in the NHS. These delays are worsened for diseases as there is often limited evidence available to meet the requirements for access and pricing decisions.

In order to get NICE to recommend that the NHS can fund their medicines, companies are required to develop a vast amount of highly specialized and detailed work which includes data collection, economic modelling and quality of life measurements, all of which can be difficult, time consuming and expensive. The processes of bodies like NICE to assess the cost effectiveness of a medicine are well established and need to be followed. However, we hope that through the collaboration in HERCULES, we can help industry better engage with this process, present relevant evidence as required and therefore enable the decision making process, and potentially speed up the time it takes for industry to engage with bodies like NICE to make decisions

HERCULES comes from a desire to help develop industry to develop this disease level evidence in collaboration, providing benefits which vary from improved modelling (reducing uncertainty), a broader evidence base, reduction of generating evidence which is duplicative or inconsistent, improved engagement with patients, lower costs and management time, additionally being ethically superior by making better use of patient input.

Duchenne UK is investing £200,000 in the initial stages of the project,


which will help companies to work together to develop a SHARED model that will focus on developing common tools and practices, including:

  • Data analysis, including mapping clinical trial endpoints to clinical outcomes
  • An HTA relevant Quality of Life metric
  • Cross-sectional study looking at the true Burden of Illness
  • Economic model for individual companies to adapt to their products
  • Training, expert input and mock appraisal committees

Emily Crossley, Duchenne UK, says: "We are delighted to be able to launch HERCULES with the support of seven industry partners, all of whom are developing treatments for DMD. In order to persuade government bodies to pay for new medicines, companies often have to provide complex data analysis and burden of care studies which are costly and time-consuming. The aim of HERCULES is for companies to collaborate together on building such models, to save time, money and ensure that the collaboration speeds up access for patients."

Josie Godfrey, ex-Director of NICE, who is running Hercules says: "HTA agencies can struggle with decisions in the absence of a solid evidence base, be that data on the burden of the disease or the likely disease progression. Through its collaboration with patient organisations, industry, universities and others partners, Hercules will ensure all companies can produce the best possible evidence for HTA agencies – making decisions easier, fairer and hopefully enabling faster access to the best new treatments for DMD."

Fleur Chandler, Future Pipeline Head, VEO at GSK R&D and a member of Duchenne UK's Patient Advisory Board says: "I'm thrilled that this initiative for collaboration across companies to support successful reimbursement is launching with Duchenne UK. It is a testament to the commitment of the companies to the Duchenne community to come together in this way and generate world-class disease level evidence for payers"

Project HERCULES coincides with the Accelerated Access Pathway initiative, which provides a fast-track route to getting 'breakthrough' treatments to patients up to four years earlier. This is part of the Government's efforts to address the long-held problem that patients often get a raw deal when accessing the latest treatments.

Phase One of Project HERCULES has begun, and working with leading academic groups will focus on understanding and synthesizing the current evidence base, the cost and burden of DMD and lives lost to it, and current measures in DMD clinical trials. The project will also look at how quality of life for boys with DMD is measured and develop a new measure as the gold standard.

Following this, the Project will map the impact of DMD on patients, families and carers, and develop a disease level economic model to support pricing and reimbursement decisions. Phase Two will be announced in 2018.

Molly Hunt
Communications Manger, Duchenne UK

Author: Magdalena Kegel
Source: Duchenne UK
2.9 from 17 votes
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