drugset / Trial / NCT05518188
Melpida: Recombinant Adeno-associated Virus (Serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt)
Phase 1/2
Recruiting
4 enrolled
Elpida Therapeutics SPC
University of Texas Southwestern Medical Center · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MELPIDA | Gene therapy (AAV / viral vector) | — | Intrathecal |