Drugs / ANB-010
last change Dec 2025 re-read 3 minutes ago

ANB-010

Gene therapy (AAV / viral vector) targets F8

Developed for
hemophilia A
Investigated by
Biocad

Trials 1

202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/2 NCT06185335 Jul 2023 → Dec 2025 overdue hemophilia A Biocad Active not recruiting No outcome recorded

Evidence & citations 4 cited values

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

FieldValueCited text
Known as ANB-010 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06185335 ↗
Modality Gene therapy (AAV / viral vector) “Adeno-associated viral vector carrying the FVIII gene single infusion at dose 1.” NCT06185335 ↗
Route Intravenous “single inravenous infusion” NCT06185335 ↗
Target F8 “Adeno-associated viral vector carrying the FVIII gene single infusion at dose 1.” NCT06185335 ↗