ASC618 Gene Therapy in Hemophilia A Patients

Recruiting now · Phase 1/Phase 2

Conditions studied: Hemophilia A

In brief

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

Key facts

Study ID
NCT04676048
Run by
ASC Therapeutics
People needed
12
Starts
2022-08-03
Expected to finish
2026-12-01
Last updated by the study team
2023-02-01

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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