Drugs / ZS801
last change Dec 2025 re-read 3 minutes ago

ZS801

Gene therapy (AAV / viral vector)

Developed for
hemophilia B
Investigated by
Institute of Hematology & Blood Diseases Hospital, China

Trials 2

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/21 trial
Phase 1/2 NCT05641610 Feb 2022 → Dec 2025 overdue hemophilia B Institute of Hematology & Blood Diseases Hospital, China Recruiting No outcome recorded
Phase not applicable1 trial
— NCT05630651 Apr 2023 → Dec 2025 overdue hemophilia B Institute of Hematology & Blood Diseases Hospital, China Recruiting No outcome recorded

Evidence & citations 4 cited values

Every value below carries the sentence it was read from. 2 sources stand behind the page.

FieldValueCited text
Known as ZS801 ClinicalTrials.gov intervention name — accepted as the source's own label NCT05630651 ↗
1

NCT05641610 ↗

Action Restore “designed to drive expression of the human factor IX (hFIX) transgene and raise circulating levels of endogenous FIX” NCT05641610 ↗
Modality Gene therapy (AAV / viral vector) “A novel, bioengineered adeno-associated viral (AAV) vector carrying human factor IX variant.” NCT05630651 ↗
Route Intravenous “Single intravenous (i.v.) infusion of ZS801” NCT05630651 ↗