| Eligibility |
Inclusion Criteria:
1. Female or male subjects who are = 18 years of age at screening;
2. Patients with a diagnosis consistent with clinically or laboratory-supported possible,
probable, or definite sporadic or familial ALSALS in accordance with Revised EI
Escorial diagnostic criteria published by the World Federation of Neurology (WFN);
3. The duration of the disease from the first symptom (any ALS symptom) prior to the
screening visit must be more than 6 months and less than 2 years (inclusive);
4. The Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R) score =30
during the screening period, and the three respiratory scores (dyspnea, upright
respiration, and respiratory insufficiency) must be full marks;
5. The forced vital capacity (FVC) of predicted during the screening period is =70% at
screening;
6. Body mass index (BMI) greater than 18 kg/m2 at screening;
7. Subjects who had not taken riluzole, edaravone, or who had been on a stable dose for
=30 days at screening and continue to take it during the study period (those who have
stopped taking riluzole, edaravone for = 30 days at screening may also be included, in
the opinion of the Investigator);
8. Understand and comply with the trial procedure, voluntarily participate in and be
willing to undergo genetic testing, and sign the informed consent (the informed
consent is voluntarily signed by the subject or the subject's leagally authorized
representative in the case that a subject is legally incapable of providing informed
consent).
Exclusion Criteria:
1. Subjects with other neurological diseases similar to ALS that affect the evaluation of
drug efficacy, such as cervical spondylotic myelopathy, syringomyelia, spinal cord and
brain stem tumors, hirayama disease, multifocal motor neuropathy, multiple sclerosis,
Guillain-Barre syndrome, Parkinson's disease and dementia;
2. Subjects who refuse to take food and medication by nasal feeding tube during the study
period due to swallowing dysfunction;
3. Subjects with a history of spinal surgery within the last six months after the onset
of ALS;
4. By cytological analysis at screening, the titer of anti-AAV9 neutralizing antibody was
positive (>1:100);
5. AST, ALT, bilirubin, glutamyltransferase, or glutamate dehydrogenase >1.5 × ULN or
serum creatinine (Scr) > ULN at screening;
6. Any medical instability deemed by the Investigator to be clinically significant,
including but not limited to the presence of cardiovascular and cerebrovascular,
hepatic or renal dysfunction, endocrine, psychiatric, or nervous system abnormalities
that the investigator believes would interfere with the overall safety or efficacy of
the study;
7. Subjects with history of convulsive seizures or epilepsy (excluding febrile convulsive
seizures in childhood);
8. History of autoimmune diseases (excluding thyroid diseases), myelodysplastic or
myeloproliferative diseases, leukemia or lymphoma, or severe scoliosis;
9. Subjects who are hospitalized for surgery, pulmonary events, or nutritional support
within 2 months prior to the screening period or who planned to undergo
hospitalization for major surgery during the study period;
10. Presence of contraindications to lumbar puncture (including, but not limited to, signs
or symptoms of skin infection at the administration site and elevated intracranial
pressure), receipt of any active intrathecal therapy, presence of implantable shunt
tubes for draining cerebrospinal fluid (CSF), presence of implantable central nervous
system (CNS) cannula, or any condition that interferes with CSF collection;
11. Screening for a record of attempted suicide in the six months prior to the screening
visit, who indicated four or five categories of suicidal thoughts on the
Columbia-Suicide Severity Rating Suicide Scale (C-SSRS) assessment, or who the
Investigator judged to be at risk of suicide attempts;
12. Active infection requiring systemic antiviral or antibacterial therapy at any time
between 4 weeks prior to the start of screening and dosing; Active but untreated viral
or bacterial infection at any time between 4 weeks prior to the start of screening and
dosing; Any febrile illness developed during the 2 weeks prior to the start of
screening until treatment was given;
13. Suspect or have a history of alcohol or drug abuse;
14. Hepatitis B virus surface antigen, hepatitis C virus antibody, syphilis, or human
immunodeficiency virus antibody positive at screening;
15. Pregnant or lactating female subjects, or subjects of childbearing potential
(including heterosexual male subjects and their fertile female partners), who have
pregnancy plans during the study period or do not want to use effective contraception
during the study period;
16. Subjects who have been received any stem cell therapy or gene therapy prior to
screening;
17. Subjects vaccinated within 2 weeks prior to screening or expected to be vaccinated
during the study period;
18. Subjects with concomitant or ongoing immunosuppressive therapy within 90 days prior to
IP administration;
19. Subjects who have participated in another clinical trial and received any
investigational therapy within 3 months prior to screening;
20. Subjects who are deemed inappropriate by the investigator to participate in this
clinical trial.
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