drugset / Trial / NCT03265119

PART A: Efficacy and Safety of AEVI-001 in Children and Adolescents With ADHD and With mGluR Mutations

NCT03265119 ↗

Phase 2 Completed 69 enrolled Aevi Genomic Medicine, LLC, a Cerecor company
RandomizedParallel-groupDouble-blindTreatment

Summary

This is PART A of a 2-part, 6-week, double-blind, dose-optimization, parallel-group study in children and adolescents (ages 6-17 years) with ADHD with and without CNVs in specific genes implicated in glutamatergic signaling and neuronal activity. Parts A will include subjects determined to have a specific gene mutations implicated in glutamatergic signaling and neuronal connectivity.

Timeline

Start
2017-08-28
Primary completion
2018-09-24
Completion
2018-10-01

Drugs

EvaluationDrugModalityDoseRoute
Subject fasoracetam Small molecule 100 mg Oral
Subject fasoracetam Small molecule 200 mg Oral
Subject fasoracetam Small molecule 400 mg Oral