Duchenne UK
Duchenne UK is a UK-registered charity funding Duchenne muscular dystrophy research and providing patient, family, and clinical support through programmes including the DMD Hub, DMD Care UK, Project HERCULES, and the Duchenne Dash fundraising event.
- Company typePrivate
- Founded2012
- HeadquartersLondon, United Kingdom
- Headcount1–10
- GTM typeB2C
- OfferingServices
What Duchenne UK does
Duchenne UK is a UK-registered charity (Charity No. 1147094, Company No. 8030768) founded in 2012 through the merger of the Duchenne Children's Trust and Joining Jack, both established by parents of children diagnosed with Duchenne muscular dystrophy (DMD), a fatal genetic muscle-wasting condition. The charity is co-led by Emily Reuben OBE and Alex Johnson OBE, with Krishnan Guru-Murthy as Chair, and operates from a small team of 1-10 employees based in Hammersmith, London. Its mission is to accelerate the search for treatments and a cure for DMD, and it is positioned as the UK's largest funder of DMD research, having deployed more than £17 million on research, clinical trial infrastructure, and patient services since 2012.
The charity's core offerings fall into three interlocking areas: (1) research funding and infrastructure, including the DMD Hub (UK clinical trial capacity expansion), Project HERCULES (collaborative health economics and patient-reported outcomes evidence generation), and grant rounds overseen by a Scientific Advisory Board of named DMD experts; (2) clinical care improvement via DMD Care UK, which issues clinical recommendations including newly launched psychosocial guidelines; and (3) direct patient and family support, comprising the Family Folder for newly diagnosed families, emergency preparedness resources (Alert Cards, steroid-dependent wristbands), the Decipha educational support partnership, the Pathfinders partnership for adult DMD patients, and events such as Parent Information Days. There is no proprietary technology product; the stack is a standard charity website, CRM-backed newsletter, event registration, and social channels.
Duchenne UK is funded entirely through donations and fundraising: individual giving, corporate Founding Patrons and Development Board relationships, family funds with branded fundraising pages, and event-driven income anchored by the annual Duchenne Dash London-Paris cycling challenge (since 2013). All family-facing resources are provided free of charge. The charity operates exclusively within the United Kingdom and is governed by a board of trustees drawn from media (Channel 4 News), law (Chatham House, Clifford Chance), accounting (KPMG), advertising (BBH, Cheil, Grace Blue), and consumer brands (Jack Wills, Aubin), supported by high-profile celebrity and athlete patrons.
Duchenne UK firmographics
Firmographics- Name
- Duchenne UK
- Legal name
- Duchenne UK
- Website
- https://duchenneuk.org
- Company type
- Private
- Founded year
- 2012
- Operating status
- Operating
- Headcount range
- 1–10 employees
- Short description
- Duchenne UK is a UK-registered charity funding Duchenne muscular dystrophy research and providing patient, family, and clinical support through programmes including the DMD Hub, DMD Care UK, Project HERCULES, and the Duchenne Dash fundraising event.
- Ownership category
- akta.pro rank
Duchenne UK industry classification
Industry- Product category
- Muscular Dystrophy Charity and Patient Support Services
- NAICS
- Voluntary Health Organizations (813212)
- akta.pro primary industry
- Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS) (BPAGACAA)
- akta.pro secondary industry
- Health & Medical Research Grantmaking Foundations (BPAGAKAL)
Keywords
Where Duchenne UK is headquartered
LocationHeadquarters
- HQ city
- London
- HQ country
- United Kingdom
- HQ region
- Europe
Offices1 record
Markets served
Duchenne UK business model
Business model- GTM type
- B2C
- Offering type
- Services
- Cost components
- Personnel, Operations, Technology or R&D, Marketing or Sales, Infrastructure
Revenue model
- Donations and Fundraising: Individual donations, corporate donations, and fundraising events including the Duchenne Dash cycling challenge. Family funds allow supporters to create dedicated fundraising pages.
- Corporate Partnerships: Development Board composed of Founding Patrons who provide donations, corporate support, connections and advice through regular giving.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| Other | One time | Free resources for families |
Go-to-market motion3 records
Distribution channels4 records
Marketing channels6 records
Duchenne UK product offering
Product offeringCore offering
Duchenne UK is a registered UK charity that funds Duchenne muscular dystrophy (DMD) research through grants and scientific advisory review, and operates clinical research infrastructure including the DMD Hub to expand patient access to clinical trials. The charity also delivers family support resources (Family Folder, emergency preparedness items, educational guides, transition guides), runs community education events (Parent Information Days, the Duchenne Dash fundraiser), and conducts patient advocacy with regulatory bodies including the FDA, EMA, MHRA, NICE and SMC.
Product overview
Duchenne UK is a non-profit charitable organization (Registered Charity No. 1147094) focused on accelerating the search for treatments and a cure for Duchenne muscular dystrophy (DMD). The organization does not offer a traditional technology product but provides a portfolio of patient support services, educational resources, and research initiatives. Key offerings include: the Family Folder (comprehensive guide for newly diagnosed families), DMD Care UK (clinical care recommendations), DMD Hub (clinical trial capacity expansion), Project HERCULES (health economics research), Parent Information Days (educational events), educational support via Decipha partnership, emergency preparedness resources (Alert Cards, steroid wristbands), guides for adolescence/financial support, and the Duchenne Dash fundraising event. The organization funds research, collaborates with scientists and pharmaceutical industry, and works with health services to improve patient care throughout the UK.
Differentiator
Problem solved
Functional benefit
Brands
- DMD Care UK: A project to improve DMD care throughout the UK by providing clinical recommendations
- DMD Hub
- Project HERCULES
Products and services
- Family Folder for Newly Diagnosed Families
Quantifiable outcome
- Over £17 million spent on DMD research since 2012
- +2 more outcomes
Companies that use Duchenne UK
Customer profileNamed customers4 records
Segments5 records
Ideal customer profiles4 records
Duchenne UK technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Duchenne UK partnerships and signals
Strategic signalPartnerships
Seven partnerships are on record, tiered core and minor.
- Action Medical ResearchcorePartnership to launch a new Research Training Fellowship opportunity in Duchenne muscular dystrophy, combining resources to support early-career researchers in the DMD field.
- DMD Care UKcoreCollaboration to improve DMD care throughout the UK by providing clinical recommendations. Project includes launch of psychosocial guidelines for the Duchenne community.
- DMD HubcoreDuchenne UK funds the DMD Hub to bring more UK patients the opportunity to take part in clinical research. The Hub expands clinical trial capacity for boys throughout the UK.
- Decipha CICcorePartnership to fund free educational support for young people with DMD. Decipha, a Community Interest Company run by DMD parents, provides assessments, specialist advice, training on SEN process including EHCPs, and dyslexia assessments.
- Pathfinders Neuromuscular AllianceminorCharity run by and for adults with neuromuscular disorders provides support for teenagers and adults with DMD on issues such as independent living, housing, employment, and welfare rights.
- Project HERCULEScoreCollaborative project to develop patient-centered outcomes and evidence for DMD treatments. Fleur Chandler from Duchenne UK chairs the Steering Group. Addresses health economics and patient-reported outcomes.
- FrankeminorCorporate sponsor whose funding has made Parent Information Days possible for Duchenne UK.
Scale indicators4 records
Recent moves6 records
Expansion highlights5 records
Duchenne UK competitors and assessment
Company assessmentDirect peers
- Parent Project Muscular Dystrophy (PPMD): US-based DMD-specific patient advocacy and research-funding charity, the leading international counterpart to Duchenne UK. Directly comparable mission and model; Alex Johnson serves on its board.
- Muscular Dystrophy UK: UK charity funding research and providing support across all neuromuscular conditions, including DMD. Directly comparable as the closest disease-overlapping UK nonprofit; competes for the same donor and corporate-partner pool.
- United Parent Projects Muscular Dystrophy (UPPMD): International umbrella organisation connecting DMD parent organisations globally; Duchenne UK's co-founder Alex Johnson sits on its board. Comparable as the international coordinating body for DMD advocacy.
- CureDuchenne: US DMD-focused charity funding research and clinical trials, including gene therapy programmes. Comparable as a single-disease DMD research and access organisation operating at international scale.
- Duchenne Parent Project Netherlands: Long-established European DMD-focused patient organisation and part of the United Parent Projects Muscular Dystrophy network. Directly comparable disease-specific advocacy and research-funding model outside the UK.
Broad incumbents
- Wellcome Trust: Major UK-based biomedical research charity and grantmaker. Relevant as a benchmark for scale of UK health research philanthropy and a potential funder/collaborator for large-scale DMD initiatives.
- Action Medical Research: UK children's medical research charity and active Duchenne UK partner (co-launched a Research Training Fellowship in DMD). Overlapping mission in paediatric disease research funding at greater scale and broader disease scope.
- Muscular Dystrophy Association (MDA): Large US neuromuscular disease charity funding research across multiple dystrophies including DMD. Overlapping research-funding mission at much larger scale and broader disease scope.
Emerging players
- Pathfinders Neuromuscular Alliance: UK charity run by adults with neuromuscular conditions providing transition/adult support; Duchenne UK partner. Comparable as a niche UK neuromuscular patient-support organisation, focused on a different life stage.
- Decipha CIC: UK Community Interest Company run by DMD parents providing educational assessments and SEN/EHCP support; Duchenne UK partner. Comparable as a complementary service provider in the DMD support ecosystem.
Market position
Strengths5 records
Weaknesses4 records
Competitive moat6 records
Key risks5 records
Key highlights7 records
Customer concentration
Duchenne UK social profiles
Digital presenceDuchenne UK financial estimates
Financial estimateRevenue estimate
Valuation estimate
Duchenne UK leadership team
Management profileNumber of profiles
Profiles8 records
Duchenne UK funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Duchenne UK M&A and investment
M&A and investmentM&A
Investments3 records
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Duchenne UK
What does Duchenne UK do?
Duchenne UK is a registered UK charity that funds Duchenne muscular dystrophy (DMD) research through grants and scientific advisory review, and operates clinical research infrastructure including the DMD Hub to expand patient access to clinical trials. The charity also delivers family support resources (Family Folder, emergency preparedness items, educational guides, transition guides), runs community education events (Parent Information Days, the Duchenne Dash fundraiser), and conducts patient advocacy with regulatory bodies including the FDA, EMA, MHRA, NICE and SMC.
Is Duchenne UK a public or private company?
Duchenne UK is a private company. It is classified as nonprofit foundation owned and is currently operating.
When was Duchenne UK founded?
Duchenne UK was founded in 2012. It employs 1 to 10 people.
Where is Duchenne UK based?
Duchenne UK is headquartered in London, United Kingdom, in the Europe region.
How does Duchenne UK make money?
Two revenue lines are on record. Donations and Fundraising is the primary driver. The others are corporate Partnerships.
Who are Duchenne UK's main competitors?
Direct peers on record are Parent Project Muscular Dystrophy (PPMD), Muscular Dystrophy UK, United Parent Projects Muscular Dystrophy (UPPMD), CureDuchenne and Duchenne Parent Project Netherlands. Broad incumbents are Wellcome Trust, Action Medical Research and Muscular Dystrophy Association (MDA). Emerging players are Pathfinders Neuromuscular Alliance and Decipha CIC.
Does Duchenne UK have an API?
No public API is recorded for Duchenne UK.
What industry is Duchenne UK in?
Duchenne UK's product category is Muscular Dystrophy Charity and Patient Support Services. Its primary akta.pro industry code is BPAGACAA, Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS), with a secondary code of BPAGAKAL, Health & Medical Research Grantmaking Foundations. Its NAICS code is 813212.