CMT Research Foundation
CMT Research Foundation is a patient-led 501(c)(3) non-profit that funds translational research across gene therapy, small molecules, and ASOs targeting Charcot-Marie-Tooth disease, serving academic researchers, biotech firms, and the CMT patient community globally.
- Company typePrivate
- Founded2018
- HeadquartersAtlanta, United States
- Headcount1–10
- GTM typeB2B
- OfferingServices
What CMT Research Foundation does
CMT Research Foundation (CMTRF) is a patient-led 501(c)(3) non-profit foundation established in 2018 and headquartered in Atlanta, Georgia. Its singular mission is to accelerate the development of treatments and cures for Charcot-Marie-Tooth (CMT) disease, an inherited peripheral neuropathy affecting approximately 3 million people worldwide for which no approved treatments exist. The foundation operates as a financial intermediary rather than a product company, funding academic researchers, biotech startups, and translational research programs that span gene therapy, small molecule drugs, antisense oligonucleotides, and drug delivery technologies across all major CMT subtypes (CMT1, CMT2, CMT4, CMTX). It partners with institutions including Johns Hopkins, Nationwide Children's Hospital, The Jackson Laboratory, the Cyprus Institute of Neurology and Genetics, and the University of Miami.
The foundation's business model combines traditional non-profit revenue streams (donations, corporate sponsorships, fundraising events such as the Alan Jackson tour generating $2.25 million) with a distinctive revenue-share model that embeds return-on-investment clauses in industry partnership contracts, recycling proceeds back into new research. Grant sizes range from $25,000 to $200,000 per year, with milestone-gated release of funds. Operating geographies span 12+ countries across North America, EMEA, and Asia Pacific. The foundation operates with a lean team of 1-10 employees and relies on a Board of Directors, Scientific Advisory Board, and Research Advisory Council for governance.
CMTRF's distribution model centers on direct enterprise sales-style grant-making to researchers and biotech firms, supplemented by the annual Global CMT Research Convention (400+ attendees in 2025) and educational channels including the CMT 101 video series and "Gene Therapies Demystified" webinars. The foundation has funded 6 therapeutics now in preclinical or active clinical trials, and two CMTRF-funded partners have achieved material commercial validation: DTx Pharma was acquired by Novartis in 2023 for $1 billion, and Augustine Therapeutics raised $85 million in Series A financing in 2024 with first patient dosed in May 2025.
CMT Research Foundation firmographics
Firmographics- Name
- CMT Research Foundation
- Legal name
- CMT Research Foundation, INC.
- Website
- https://cmtrf.org
- Company type
- Private
- Founded year
- 2018
- Operating status
- Operating
- Headcount range
- 1–10 employees
- Short description
- CMT Research Foundation is a patient-led 501(c)(3) non-profit that funds translational research across gene therapy, small molecules, and ASOs targeting Charcot-Marie-Tooth disease, serving academic researchers, biotech firms, and the CMT patient community globally.
- Ownership category
- akta.pro rank
CMT Research Foundation industry classification
Industry- Product category
- Rare Disease Research Funding
- NAICS
- Voluntary Health Organizations (813212)
- akta.pro primary industry
- Health & Medical Research Grantmaking Foundations (BPAGAKAL)
- akta.pro secondary industry
- Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS) (BPAGACAA)
Keywords
Where CMT Research Foundation is headquartered
LocationHeadquarters
- HQ city
- Atlanta
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
CMT Research Foundation business model
Business model- GTM type
- B2B
- Offering type
- Services
- Cost components
- Technology or R&D, Personnel, Marketing or Sales, Operations, Others
Revenue model
- Donations and Charitable Contributions: The foundation raises funds through donations from individuals, corporate sponsors, and fundraising events (such as Alan Jackson's concert tour which raised $2.25 million). The foundation also receives grants from patient advocacy groups and co-funding partners.
- Revenue Share Program: The foundation forges partnerships that include revenue share arrangements. Every contract includes a return on the Research Foundation's initial investment which is then reinvested in new research projects. This creates a sustainable funding cycle for CMT research.
Go-to-market motion1 record
Distribution channels4 records
Marketing channels8 records
CMT Research Foundation product offering
Product offeringCore offering
CMT Research Foundation funds translational and preclinical research for Charcot-Marie-Tooth disease through grants of typically $25,000–$200,000 per year to academic labs and biotech companies. It maintains a CMT Research Pipeline tracker and a Clinical Trial Finder, and convenes an annual Global CMT Research Convention. It supplements donations with a revenue-share partnership program that returns a portion of downstream licensing income back to the foundation.
Product overview
CMT Research Foundation operates as a patient-led non-profit organization focused on funding CMT (Charcot-Marie-Tooth disease) research rather than selling a traditional product. Its core offerings include research funding programs with grants ranging from $25,000 to $200,000+ per year, a comprehensive CMT Research Pipeline tracking therapies under development across small molecule, gene therapy, and biologics categories, a Clinical Trial Finder directory, educational content including the CMT 101 Video Series, and the annual Global CMT Research Convention. The foundation connects researchers, clinicians, biotech companies, and patients to accelerate treatments and cures for all types of CMT.
Differentiator
Problem solved
Functional benefit
Products and services
- CMT Research Funding Programs Milestone-gated research grants (typically $25,000–$200,000 per year) awarded to academic labs and biotech companies working on gene therapy, antisense oligonucleotides, small molecules, drug delivery, and biomarkers for Charcot-Marie-Tooth disease. Intended for academic principal investigators, translational researchers, and biotech/pharma R&D teams.
- CMT Research Pipeline A research pipeline database that tracks the status of CMT research programs funded by or affiliated with the foundation, available on the CMTRF website. Intended for researchers, clinicians, patients, and donors seeking transparency into active CMT programs.
- CMT Clinical Trial Finder An online directory of clinical trials relevant to CMT patients, accessible through the foundation's website. Intended for patients, families, and clinicians seeking enrollment information for CMT-related trials.
- Global CMT Research Convention Annual international convention organized by the foundation that convenes CMT researchers, clinicians, biotech and pharma partners, and patient community members to share research progress and foster collaboration. Intended for the global CMT research and patient community.
- Industry Partnership / Revenue-Share Program Formal partnership program with biotech and pharmaceutical companies in which CMTRF co-funds CMT research and receives a percentage of any downstream licensing income generated from resulting programs. Intended for biotech and pharmaceutical business development and R&D leaders.
Quantifiable outcome
- 6 therapeutics advanced to preclinical or active clinical trials through CMTRF funding
- +3 more outcomes
Companies that use CMT Research Foundation
Customer profileNamed customers4 records
Segments3 records
Ideal customer profiles3 records
CMT Research Foundation technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
CMT Research Foundation partnerships and signals
Strategic signalPartnerships
14 partnerships are on record, tiered core, major and minor.
- Novartis (via DTx Pharma)coreCMTRF introduced DTx Pharma to CMT research and funded their first CMT research with a grant of $128,000. DTx Pharma developed a platform called FALCON (Fatty Acid Ligand Conjugated Oligonucleotide) to deliver RNA therapeutics to peripheral nerves. Novartis acquired DTx Pharma in 2023 for $1 billion and is now advancing the CMT1A drug candidate EKD060 to clinical trials.
- Augustine TherapeuticscoreCMTRF helped Augustine Therapeutics underwrite the development of novel HDAC6 inhibitor drugs for CMT1A. Augustine completed Series A financing of $85 million and advanced lead candidate AGT-100216 to Phase 1 clinical trial, with first patient dosed in May 2025.
- Armatus BiocoreCMTRF-funded research from Dr. Kleopa (Cyprus Institute of Neurology and Genetics) and Dr. Harper (Nationwide Children's Hospital) was licensed to Armatus Bio. The gene therapy ARM-101 for CMT1A is preparing for clinical trials after successful preclinical studies.
- Elpida TherapeuticscoreCMTRF provided $800,000 and CureCMT4J provided $700,000 to Elpida Therapeutics to launch manufacturing of gene therapy drug ELP-02 for CMT4J. Phase I/II trial planned for early-mid 2026.
- Johns Hopkins UniversitymajorActive project: Find a blood-based biomarker that could measure whether future CMT treatments are working. Project led by Jeremy Sullivan and Charlotte Sumner.
- Nationwide Children's HospitalmajorMultiple active projects including gene therapy development for CMT1B by Dr. Afrooz Rashnonejad, and AAV delivery optimization for Schwann cells. Dr. Scott Harper collaborated on CMT1A gene therapy later licensed to Armatus Bio.
- Cyprus Institute of Neurology and GeneticsmajorDr. Kleopas Kleopa developed gene therapy approach for CMT1A that was funded by CMTRF and later licensed to Armatus Bio. Research focused on lowering PMP22 protein levels in peripheral nerves.
- The Jackson LaboratorymajorDeveloping humanized mouse models for CMT1B that express human MPZ gene to study disease mechanisms and accelerate drug development.
- University of MiamimajorDr. Stephan Zuchner developing mouse model of CMT1J and testing RNA therapeutic approach. Collaboration with 1J Foundation.
- ReviR TherapeuticsmajorDeveloping small molecule splice modulators for CMT1A that reduce expression of overexpressed PMP22 gene. Program paused as ReviR focuses on advancing a clinical-stage molecule for CMT.
- AcuraStem (Licensed to Takeda)majorCMTRF funded underlying technology for PIKfyve inhibitor targeting axon degeneration in CMT2A. Technology licensed to Takeda in September 2023. Provisional patent filed May 2023.
- Shift PharmaceuticalsmajorDeveloping morpholino-based antisense oligonucleotides (PMO ASOs) targeting excess PMP22 protein for CMT1A treatment. Lead drug candidate identified and advancing toward clinical trials.
- Nanite Inc.minorDeveloping polymer nanoparticles (PNPs) for drug delivery across the blood-nerve barrier to deliver genetic therapies to Schwann cells. Project closed; Nanite evaluating next strategic step.
- Peripheral Nerve SocietymajorCMTRF research team attends annual Peripheral Nerve Society conference in the Netherlands to learn about latest advances, network with field leaders, and accelerate CMT treatment progress.
Scale indicators6 records
Recent moves6 records
Expansion highlights6 records
CMT Research Foundation competitors and assessment
Company assessmentDirect peers
- Charcot-Marie-Tooth Association (CMTA): The other primary U.S.-based nonprofit solely dedicated to CMT, funding research, patient support, and clinician education. Highly comparable as a fellow disease-specific CMT research foundation with overlapping mission.
- Hereditary Neuropathy Foundation (HNF): Patient-led nonprofit focused on Charcot-Marie-Tooth disease and inherited neuropathies. Directly comparable in mission (CMT cures), funding model (research grants, industry partnerships), and patient community engagement.
Broad incumbents
- Cystic Fibrosis Foundation: Pioneer of the disease-specific research funding model that led to multiple approved therapies. Comparable as a large-scale patient-led research foundation with venture philanthropy and revenue-share models that CMTRF explicitly mirrors.
- Muscular Dystrophy Association (MDA): Major nonprofit funding research across neuromuscular diseases including CMT. Comparable in mission to accelerate treatments for neuromuscular conditions, though broader than CMTRF's CMT-only focus.
- National Organization for Rare Disorders (NORD): Umbrella organization for rare disease patient groups. CMTRF holds NORD Platinum membership. Comparable as a research-funding and advocacy nonprofit in the rare disease space, though operating at much broader scale.
- ALS Association: Major patient-led nonprofit funding ALS/MND research globally with active industry partnerships. Comparable in patient-led research funding model and disease-specific drug development focus, though operating at much larger scale.
Emerging players
- Cure SMA: Patient-led nonprofit that funded spinal muscular atrophy research leading to approved gene therapies (Spinraza, Zolgensma). Highly comparable disease-specific research foundation model with similar revenue share and milestone-gated grant approach.
- Friedreich's Ataxia Research Alliance (FARA): Patient-driven rare disease research foundation funding drug development for Friedreich's ataxia. Comparable in scale, mission, and patient-led research funding approach for a rare inherited neurological disease.
- Parent Project Muscular Dystrophy (PPMD): Disease-specific nonprofit funding Duchenne muscular dystrophy research with venture philanthropy elements. Comparable in using milestone-gated grants, industry partnerships, and patient community leverage to drive drug development.
- Myelin Repair Foundation: Patient-focused foundation funding translational research on myelin-related disorders including peripheral neuropathies. Directly relevant given CMT's underlying demyelination pathology, though operating in adjacent rather than identical disease space.
Market position
Strengths4 records
Weaknesses4 records
Competitive moat5 records
Key risks5 records
Key highlights7 records
Customer concentration
CMT Research Foundation social profiles
Digital presenceCMT Research Foundation financial estimates
Financial estimateRevenue estimate
Valuation estimate
CMT Research Foundation leadership team
Management profileNumber of profiles
Profiles3 records
CMT Research Foundation funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
CMT Research Foundation M&A and investment
M&A and investmentM&A
Investments6 records
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about CMT Research Foundation
What does CMT Research Foundation do?
CMT Research Foundation funds translational and preclinical research for Charcot-Marie-Tooth disease through grants of typically $25,000–$200,000 per year to academic labs and biotech companies. It maintains a CMT Research Pipeline tracker and a Clinical Trial Finder, and convenes an annual Global CMT Research Convention. It supplements donations with a revenue-share partnership program that returns a portion of downstream licensing income back to the foundation.
Is CMT Research Foundation a public or private company?
CMT Research Foundation is a private company. It is classified as nonprofit foundation owned and is currently operating.
When was CMT Research Foundation founded?
CMT Research Foundation was founded in 2018. It employs 1 to 10 people.
Where is CMT Research Foundation based?
CMT Research Foundation is headquartered in Atlanta, United States, in the North America region.
How does CMT Research Foundation make money?
Two revenue lines are on record. Donations and Charitable Contributions are the primary driver. The others are revenue Share Program.
Who are CMT Research Foundation's main competitors?
Direct peers on record are Charcot-Marie-Tooth Association (CMTA) and Hereditary Neuropathy Foundation (HNF). Broad incumbents are Cystic Fibrosis Foundation, Muscular Dystrophy Association (MDA), National Organization for Rare Disorders (NORD) and ALS Association. Emerging players are Cure SMA, Friedreich's Ataxia Research Alliance (FARA), Parent Project Muscular Dystrophy (PPMD) and Myelin Repair Foundation.
Does CMT Research Foundation have an API?
No public API is recorded for CMT Research Foundation.
What industry is CMT Research Foundation in?
CMT Research Foundation's product category is Rare Disease Research Funding. Its primary akta.pro industry code is BPAGAKAL, Health & Medical Research Grantmaking Foundations, with a secondary code of BPAGACAA, Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS). Its NAICS code is 813212.