Drugs / FLT190
last change Sep 2023 re-read 3 minutes ago

FLT190

Gene therapy (AAV / viral vector) targets GLA

Developed for
Fabry disease
Investigated by
Spur Therapeutics

Trials 2

2020202120222023202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/2 NCT04455230 Sep 2020 → Sep 2023 Fabry disease Spur Therapeutics Completed No outcome recorded
Phase 1/2 NCT04040049 Jul 2019 → May 2023 Fabry disease Spur Therapeutics Terminated No outcome recorded

Evidence & citations 4 cited values

Every value below carries the sentence it was read from. 3 sources stand behind the page.

FieldValueCited text
Known as FLT190 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04040049 ↗
1

NCT04455230 ↗

Modality Gene therapy (AAV / viral vector) “FLT190 is a recombinant adeno- associated viral (AAV) vector.” NCT04040049 ↗
Route Intravenous “On Day 0, FLT190 will be administered as a single dose, slow intravenous infusion.” NCT04040049 ↗
Target GLA “FLT190 consists of a potent, synthetic capsid (AAVS3) containing an expression cassette with a codon-optimized human GLA cDNA under the control of a liver-specific promoter...” PMID 36631545 ↗ Jan 2023