A Trial of CM-AT in Children With Autism- Open Label Extension Study
Status: | Completed |
---|---|
Conditions: | Neurology, Psychiatric, Autism |
Therapuetic Areas: | Neurology, Psychiatry / Psychology |
Healthy: | No |
Age Range: | 9 - 12 |
Updated: | 3/3/2019 |
Start Date: | January 2010 |
End Date: | February 2016 |
A Phase III Open Label Extension Study of CM-AT in Children With Autism
The purpose of this study is to determine whether CM-AT is effective in treating the core
symptoms of autism.
symptoms of autism.
Autism is currently a significant cause of disability in the pediatric population. CM-AT is
based upon the observation that many children with autism do not digest protein. CM-AT is a
proprietary enzyme that is designed as a powder taken three times a day. It is formulated to
be released in the small intestine to enhance protein digestion thus increasing the
availability of essential amino acids.
based upon the observation that many children with autism do not digest protein. CM-AT is a
proprietary enzyme that is designed as a powder taken three times a day. It is formulated to
be released in the small intestine to enhance protein digestion thus increasing the
availability of essential amino acids.
Inclusion Criteria:
- Meets the current Diagnostic and Statistical Manual for Mental Disorders (DSM-IV-TR)
diagnostic criteria for autistic disorder (AD)
- Ongoing 00102 Protocol required completion of 00101 Protocol
- Now recruiting subjects directly into 00102 Protocol
Exclusion Criteria:
- Ongoing study required patients to be 3-8 years old weighing < 11kg (24.2 lbs.), and
achieving ages 9-12 years old weighing < 22kg (48.4 lbs.).
- Newly recruited subjects must be between ages 9 - 12 years old weighing < 22kgs (48.4
lbs.)
- Demonstrated previous allergy to porcine (pork) products
- Previous history of severe head trauma or stroke, seizure within one year of entering
study or uncontrolled systemic disease
- Diagnosis of: HIV, cerebral palsy, endocrine disorder, pancreatic disease
- Within 30 days of starting the study, certain supplementation, chelation or dietary
restriction (a 30 day washout period would be required for inclusion)
- Any use of psychotropic medications, stimulants, or SSRI's must be discontinued for 30
days prior to entrance
We found this trial at
19
sites
Saint Peter's University Hospital Located in New Brunswick, NJ, Saint Peter's University Hospital has been...
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University of North Carolina at Chapel Hill Carolina’s vibrant people and programs attest to the...
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Ohio State University The Ohio State University’s main Columbus campus is one of America’s largest...
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