Recruiting
Phase 1
Phase 2

MELPIDA

Sponsor:

Elpida Therapeutics SPC

Code:

NCT05518188

Conditions

Spasticity, Muscle

Microcephaly

Intellectual Deficiency

Growth Retardation

SPG50

Eligibility Criteria

Sex: All

Age: 0 - 10

Healthy Volunteers: Not accepted

Interventions

MELPIDA

Study Details

Brief 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.

Conditions

Spasticity, Muscle

Microcephaly

Intellectual Deficiency

Growth Retardation

SPG50

Study ID

NCT05518188

Start date

Feb 15, 2023

Status verified date

Jul, 2026

Completion date

Oct 1, 2030

Anticipated

Primary completion date

Oct 1, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0 - 10

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Age 4 months-10 years old
2. Confirmed diagnosis of SPG50 disease by:

1. Genomic DNA mutation analysis demonstrating homozygous or compound heterozygous, confirmed pathogenic variants in the AP4M1 gene
2. Clinical history or examination features consistent with SPG50 and that include neurologic dysfunction
3. Parent/legal guardian willing to provide written informed consent for their child prior to participation in the study
4. Subject able to comply with all protocol requirements and procedures
5. Ability to stand for more than 5 seconds OR
6. Ability to take 5 steps independently or with a walker OR
7. Modified Ashworth Scale score 2 or below (Ankles).

Exclusion Criteria:

1. Inability to participate in study procedures (as determined by the site investigator)
2. Presence of a concomitant medical condition that precludes lumbar puncture (LP) or use of anesthetics
3. History of bleeding disorder or any other medical condition or circumstance in which lumbar puncture is contraindicated according to local institutional policy
4. Inability to be safely sedated in the opinion of the clinical anesthesiologist
5. Active infection, at the time of dosing, based on clinical observations
6. Concomitant illness or requirement for chronic drug treatment that in the opinion of the PI creates unnecessary risks for gene transfer
7. Inability of the patient to undergo MRI according to local institutional policy
8. Inability of the patient to undergo any other procedure required in this study
9. The presence of significant non-SPG50 related CNS impairment or behavioral disturbances that would confound the scientific rigor or interpretation of results of the study
10. Have received an investigational drug within 30 days prior to screening or plan to receive an investigational drug (other than gene therapy) during the study.
11. Enrollment and participation in another interventional clinical trial
12. Contraindication to MELPIDA or any of its ingredients
13. Contraindication to any of the immune suppression medications used in this study
14. Clinically significant abnormal laboratory values (GGT, ALT, and AST, or total bilirubin \> 3 × ULN, creatinine ≥ 1.5 mg/dL, hemoglobin \[Hgb\] \< 6 or \> 20 g/dL; white blood cell \[WBC\] \> 20,000 per cmm) prior to gene replacement therapy.

Study Design

Enrollment

4 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Treatment Arm

MELPIDA, a gene therapy product

Interventions

MELPIDA

MELPIDA, a recombinant serotype 9 adeno-associated virus (AAV) encoding a codon-optimized human AP4M1 transgene

Primary outcome measure

  • Incidence of unanticipated treatment-related toxicities, Grade 3 or higher in participants with SPG50 [ Time Frame: 60 months ]

Central Contacts and Locations

Central contacts

Locations

Children's Medical Center Dallas

Recruiting

Dallas, Texas, United States, 75235

Contacts

More Information

Sponsor

Elpida Therapeutics SPC

Last update posted

Jul 8, 2026

Last verified

Jul, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Elpida Therapeutics SPC on 2026-07-08.