Drugs / LE051
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LE051

Gene therapy (AAV / viral vector)

Developed for
Duchenne muscular dystrophy
Investigated by
Shanghai Jiao Tong University School of Medicine

Trials 1

20252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 0 NCT06900049 Oct 2024 → Sep 2026 overdue Duchenne muscular dystrophy Shanghai Jiao Tong University School of Medicine 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 LE051 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06900049 ↗
Modality Gene therapy (AAV / viral vector) “delivered via adeno-associated virus” NCT06900049 ↗
Route Intravenous “single intravenous infusion” NCT06900049 ↗