drugset / Trial / NCT05518188

Melpida: Recombinant Adeno-associated Virus (Serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt)

NCT05518188 ↗

NaSingle-groupOpen-labelTreatment

Summary

MELPIDA is proposed for the treatment of subjects with SPG50 and targets neuronal cells to deliver a fully functional human AP4M1 cDNA copy via intrathecal injection to counter the associated neuronal loss. Outcomes will evaluate the safety and tolerability of a single dose of MELPIDA, which will be measured by the treatment-associated adverse events (AEs) and serious adverse events (SAEs). Secondarily, the trial will explore efficacy in terms of disease burden assessments.

Timeline

Start
2023-02-15
Primary completion
2028-10-01
Completion
2030-10-01

Drugs

EvaluationDrugModalityDoseRoute
Subject MELPIDA Gene therapy (AAV / viral vector) — Intrathecal