Groundbreaking gene therapy trial set to cure haemophilia
Posted: 14 December 2017 | Drug Target Review | No comments yet
A cure for haemophilia is one step closer, following results of a gene therapy trial led by the NHS in London.


Clinical researchers at Barts Health NHS Trust and Queen Mary University of London have found that over one year on from a single treatment with a gene therapy drug, participants with haemophilia A (the most common type) are showing normal levels of the previously missing protein, and effectively curing them.
A single infusion of the gene therapy drug showed improved levels of the essential blood clotting protein factor VIII, with 85 per cent of patients achieving normal or near-normal factor VIII levels even many months after treatment.
The results have particular significance as the first successful gene therapy trial for haemophilia A.
Biomarkers aren’t just supporting drug discovery – they’re driving it
FREE market report
From smarter trials to faster insights, this report unpacks the science, strategy and real-world impact behind the next generation of precision therapies.
What you’ll unlock:
- How biomarkers are guiding dose selection and early efficacy decisions in complex trials
- Why multi-omics, liquid biopsy and digital tools are redefining the discovery process
- What makes lab data regulatory-ready and why alignment matters from day one
Explore how biomarkers are shaping early drug development
Access the full report – it’s free!
The results are published in the New England Journal of Medicine.
There are around 2,000 people with severe haemophilia A in the UK. A hereditary genetic condition dominantly affecting men, people with severe haemophilia A have virtually none of the protein factor VIII which is essential for blood to clot. It puts those affected at risk of excessive bleeding even from the slightest injury as well as causing spontaneous internal bleeding, which can be life-threatening. Recurring bleeding into joints can also lead to progressive joint damage and arthritis. The only current treatment involves multiple weekly injections to control and prevent bleeding, but there is no cure.
The trial saw patients across England injected with a copy of the missing gene, which allows their cells to produce the missing clotting factor. Following patients for up to 19 months, tests show that 11 out of 13 patients in the trial now have normal or near normal levels of the previously missing factor and all 13 patients have been able to stop their previously regular treatment.
Professor John Pasi, Haemophilia Centre Director at Barts Health NHS Trust and Professor of Haemostasis and Thrombosis at Queen Mary University of London explained:
“When we started out we thought it would be a huge achievement to show a five per cent improvement, so to actually be seeing normal or near normal factor levels with dramatic reduction in bleeding is quite simply amazing.”
The team will now hold further tests widening participants globally to include people in the USA, Europe, Africa and South America.
The five UK trial sites included The Royal London, Guys and St Thomas’, Birmingham, Cambridge and Hampshire hospitals.
Related topics
Disease Research, Gene Therapy, Protein
Related conditions
Haemophilia
Related organisations
Barts Health NHS Trust, NHS, Queen Mary University of London
Related people
John Pasi