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Clinical Trial 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 and 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05067582
Study type Interventional
Source Yamo Pharmaceuticals LLC
Contact Uyen Nguyen
Phone 949-769-0046
Email [email protected]
Status Not yet recruiting
Phase Phase 2
Start date October 2021
Completion date March 2023

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