Drugs / ASC618
last change Dec 2023 re-read 3 minutes ago

ASC618

Gene therapy (AAV / viral vector)

Developed for
hemophilia A
Investigated by
ASC Therapeutics

Trials 1

2023202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/2 NCT04676048 Aug 2022 → Dec 2023 overdue hemophilia A ASC Therapeutics Recruiting No outcome recorded

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as ASC618 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04676048 ↗
Modality Gene therapy (AAV / viral vector) “ASC618, an AAV vector encoding B-domain deleted codon-optimized human factor VIII” NCT04676048 ↗
Route Intravenous “ASC618 will be given as a single IV infusion” NCT04676048 ↗