drugset / Trial / NCT05067582
A 12-Week Crossover Study to Assess the Efficacy, Safety and Tolerability of L1-79 in Subjects Aged 12-21 Years With Autism Spectrum Disorder
RandomizedCrossoverQuadruple-blindTreatment
Summary
This study will investigate the efficacy, safety and tolerability of L1-79 in participants aged 12-21 years who have been diagnosed with ASD with a score of \>/= 70 on the Wechsler Abbreviated Scale of Intelligence (WASI-II), and a score of \>/= 4 on the Clinical Global Impression of Severity of Illness (CGI-S) weighted for socialization.
Timeline
- Start
- 2022-01-25
- Primary completion
- 2024-06-18
- Completion
- 2024-06-21
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | L1-79 | Unknown | 200 mg | Oral |
| Subject | L1-79 | Unknown | 300 mg | Oral |