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Clinical Trial Summary

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


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04676048
Study type Interventional
Source ASC Therapeutics
Contact Clinical Trial Manager, PhD
Phone (408) 495-3891
Email gil.gonen@asctherapeutics.com
Status Recruiting
Phase Phase 1/Phase 2
Start date August 3, 2022
Completion date December 2026

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