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

NCT05067582

Phase 2 Completed 58 enrolled Yamo Pharmaceuticals LLC
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

EvaluationDrugModalityDoseRoute
Subject L1-79 Unknown 200 mg Oral
Subject L1-79 Unknown 300 mg Oral

Indications