Currently, hemophilia A patients are managed with prophylactic or on-demand replacement therapy with recombinant FVIII or alternative therapeutics. The major challenges of current treatment regimens, such as the short half-life of hemophilia therapeutics with the need for frequent IV injections, encourage the current efforts for gene transfer therapy. This study will evaluate the safety and preliminary efficacy of ASC618, an AAV vector encoding B-domain deleted codon-optimized human factor VIII under a synthetic liver-directed promoter
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
12
ASC618 will be given as a single IV infusion
Arkansas Children's Hospital
Little Rock, Arkansas, United States
RECRUITINGNumber of adverse events, and serious AEs
Time frame: 12 months post-infusion
Changes in FVIII activity levels from baseline
Time frame: 12 months post-infusion
Annualized FVIII consumption
Time frame: 12 months post-infusion
Annualized bleeding rate (ABR)
Time frame: 12 months post-infusion
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.