Background: Despite improvements in hemophilia care, challenges remain, including treatment burden and impaired quality of life. Gene therapy may overcome these. However, its introduction presents a challenge.Objectives: To outline a function-based gene therapy working model describing critical milestones associated with gene therapy handling, administration, and follow-up to facilitate and implement an effective infrastructure for gene therapy introduction.Design: Literature review and consensus discussion among Hemophilia Comprehensive Care centers (HCCCs) in the Nordic region.Methods: Representatives from six HCCCs sought to pinpoint milestones and key stakeholders for site readiness at the pre-, peri-, and post-infusion stages, includin...
Background: Gene therapy trial results show potential to cure haemophilia A and haemophilia B. Secur...
Gene therapy has the potential to revolutionise treatment for patients with haemophilia and is close...
Gene therapy may be the next major advance for treatment of many diseases, and severe haemophilia (a...
Comprehensive, integrated care provided by a multi-disciplinary team of experts improves outcomes an...
INTRODUCTION: With approval of gene therapy for haemophilia likely in the near future, policy framew...
Hemophilia is a monogenic disease with robust clinicolaboratory correlations of severity. These attr...
Introduction: Adeno-associated virus (AAV)-based gene therapy for haemophilia presents a challenge t...
Introduction: Adeno-associated virus (AAV)-based gene therapy for haemophilia presents a challenge t...
Gene therapy has recently become a realistic treatment perspective for patients with haemophilia. Re...
The last two decades has seen significant progress in the treatment of hemophilia A. The developmen...
Introduction: Adeno-associated virus (AAV)-based gene therapy for haemophilia presents a challenge t...
With liver-directed gene therapy, congenital haemophilia has the potential to progress from an incur...
Hemophilia is an inherited bleeding disorder caused by the lack of a protein necessary for blood clo...
Historically, the standard of care for hemophilia A has been intravenous administration of exogenous...
Gene therapy is an appealing prospect for the treatment of human diseases. In this chapter, I will d...
Background: Gene therapy trial results show potential to cure haemophilia A and haemophilia B. Secur...
Gene therapy has the potential to revolutionise treatment for patients with haemophilia and is close...
Gene therapy may be the next major advance for treatment of many diseases, and severe haemophilia (a...
Comprehensive, integrated care provided by a multi-disciplinary team of experts improves outcomes an...
INTRODUCTION: With approval of gene therapy for haemophilia likely in the near future, policy framew...
Hemophilia is a monogenic disease with robust clinicolaboratory correlations of severity. These attr...
Introduction: Adeno-associated virus (AAV)-based gene therapy for haemophilia presents a challenge t...
Introduction: Adeno-associated virus (AAV)-based gene therapy for haemophilia presents a challenge t...
Gene therapy has recently become a realistic treatment perspective for patients with haemophilia. Re...
The last two decades has seen significant progress in the treatment of hemophilia A. The developmen...
Introduction: Adeno-associated virus (AAV)-based gene therapy for haemophilia presents a challenge t...
With liver-directed gene therapy, congenital haemophilia has the potential to progress from an incur...
Hemophilia is an inherited bleeding disorder caused by the lack of a protein necessary for blood clo...
Historically, the standard of care for hemophilia A has been intravenous administration of exogenous...
Gene therapy is an appealing prospect for the treatment of human diseases. In this chapter, I will d...
Background: Gene therapy trial results show potential to cure haemophilia A and haemophilia B. Secur...
Gene therapy has the potential to revolutionise treatment for patients with haemophilia and is close...
Gene therapy may be the next major advance for treatment of many diseases, and severe haemophilia (a...