drugset / Trial / NCT02286817

Phase I Single Dose, Open-Label Pharmacokinetic Study and Single-Blind, Placebo-Controlled Dose Escalation Study of NFC-1 in Adolescents With Attention-Deficit Hyperactivity Disorder

NCT02286817 ↗

NaSingle-groupOpen-labelTreatment

Summary

This trial is a Phase 1 study in adolescents with ADHD and genetic disruptions impacting genes in the metabotropic glutamate receptor (mGluR) network. The objectives of the study are to evaluate the safety, tolerability, and pharmacokinetics following single-dose, oral administration of NFC-1 and to evaluate safety and tolerability and to obtain evidence for the effect of NFC-1 on ADHD severity and global functioning during and following four weeks of continuous treatment. Exploratory analyses will be performed to assess effect size of specific mGluR-network genes on ADHD based on responsiveness of patients to NFC-1. This study will be conducted at a single clinical site, the Jefferson University Hospital PKU (Philadelphia, PA).

Timeline

Start
2015-01
Primary completion
2015-05
Completion
2016-03

Drugs

EvaluationDrugModalityDoseRoute
Subject fasoracetam Small molecule 50 mg Oral
Subject fasoracetam Small molecule 400 mg Oral
Subject fasoracetam Small molecule 800 mg Oral