Transforming the Future of Liver and Rare Genetic Disorder Treatments
Driving innovation in gene therapy, RNA therapeutics, and targeted drug delivery – for every patient, everywhere.

Our Mission

Advancing Science, Changing Lives through collaborative research and innovative treatments

Accelerate Research

Fast-track innovative therapies from lab to clinic through cutting-edge research and development.

Empower Patients

Advocate and create global access to treatments for those affected by rare genetic disorders.

Collaborate Globally

Partner with researchers, biotech companies, and governments to drive medical breakthroughs.

Our Focus Areas

Targeting the most challenging unmet needs in medicine

Liver Cancer & Liver Failure

Including hepatocellular carcinoma and advanced cirrhosis

Metabolic Liver Diseases

NAFLD, NASH, and metabolic syndrome research

Rare Genetic Disorders

MPS, lysosomal storage diseases, and genetic syndromes

Neurological Disorders

Parkinson's, Alzheimer's, and Huntington's disease

First Gene Therapy Trials
First-in-human clinical trials of gene therapy for liver cancer in the UK
Habib 4X Device
Development of bipolar radiofrequency device for bloodless liver surgery
RNA Aptamer Systems
Breakthrough research in RNA aptamer-based delivery systems for targeted therapy
Global Partnerships
Establishment of worldwide research collaborations and clinical networks

Our Approach

From Lab to Life – A comprehensive pipeline ensuring breakthrough treatments reach patients

Precision-Targeted Therapeutics

Developing treatments that target specific molecular pathways

Global Collaborations

Partnerships with leading institutions worldwide

Rigorous Clinical Standards

Maintaining the highest safety and efficacy standards

Equitable Access

Ensuring treatments reach patients regardless of location

We believe in the power of partnerships to deliver medical breakthroughs faster

Collaborating with academic institutions, biotechnology companies, and healthcare systems worldwide

Patient Stories & Advocacy

Real stories of hope, progress, and resilience

Accelerate Research

Living with MPS I, Emma's family found hope through our research programs and patient advocacy initiatives.

Michael's Recovery

After participating in our liver cancer gene therapy trial, Michael's life was transformed.

The Rodriguez Family

Finding community and support through our rare disease advocacy programs and research initiatives.

How You Can Help

Join us in bringing hope to those living with life-limiting conditions

Donate

Support research and clinical trials that can change lives

Partner

Collaborate with us to develop new therapies

Volunteer

Contribute your expertise to our advocacy programmes

News & Updates

Stay informed about our latest research and breakthroughs
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Press Release

Dawn Therapeutics Announces New Preclinical Data for DTX-101

25 July 2025
Early-stage results show targeted enzyme delivery to brain and cartilage in Hurler Syndrome model.
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Publication

Targeted Lentiviral Vectors for CNS and Musculoskeletal Disorders

15 June 2025
Peer-reviewed article in Molecular Therapy outlines the platform’s potential across multiple indications.
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Conference

Dawn Presents at the Annual Gene Therapy Symposium

21 May 2025
CEO delivers keynote on next-generation targeted delivery systems.
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