Predicting Treatment Response to Memantine in Autism Using Magnetic Resonance Spectroscopy

EARLY_PHASE1CompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

June 30, 2016

Primary Completion Date

April 30, 2021

Study Completion Date

April 30, 2021

Conditions
Autism Spectrum Disorder
Interventions
DRUG

Memantine

Namenda (pill and the liquid) will be started at 5 mg/day doses to be titrated up 20 mg/day based on response and tolerability, as per the package insert instructions and based upon clinical titration in other clinical trials for a period of 12 weeks. Namenda XR will be started at 7 mg/day to be titrated up to 28mg/day based on response and tolerability, as per package insert instructions and based upon clinical titration in other clinical trials for a period of 12 weeks.

DEVICE

Magnetic Resonance Imaging

The subjects will undergo an MRI assessment after baseline behavioral assessment. The session will involve a structural MRI scan, single voxel spectroscopy scans and resting state functional MRI. The subjects will be started on memantine post the imaging session. The imaging will be carried out on a research dedicated 3 Tesla (3T) Siemens Trio Scanner at the University of Missouri Brain Imaging Center by trained personnel.

Trial Locations (1)

65211

University of Missouri, Columbia

All Listed Sponsors
lead

University of Missouri-Columbia

OTHER

NCT02811627 - Predicting Treatment Response to Memantine in Autism Using Magnetic Resonance Spectroscopy | Biotech Hunter | Biotech Hunter