Autism Clinical Trial
Official title:
An Open-Label Extension Study of CM-AT for the Treatment of Children With Autism With All Levels of Fecal Chymotrypsin
Verified date | October 2023 |
Source | Curemark |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a Phase III, open label extension study evaluating the continued safety and efficacy of CM-AT in pediatric patients with autism with all levels of fecal chymotrypsin.
Status | Active, not recruiting |
Enrollment | 405 |
Est. completion date | January 2025 |
Est. primary completion date | January 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 3 Years to 17 Years |
Eligibility | Inclusion Criteria: - Age between 3 and 8 years, inclusive, at the time of signing informed consent/assent in Sponsor 00103 Study - Completion of the Sponsor's 00103 Study who continue to meet eligibility requirements - Currently in the 00102 open label study and continue to meet eligibility requirements - Subjects who initially qualified for 00103 screening, who subsequently failed Baseline entrance criteria for randomization (@Visit 1) Baseline assessment of the ABC eligibility requirement who continue to meet eligibility requirements - Up to 20 subjects 9-17 years of age who directly enroll into this study, who meet the current Diagnostic and Statistical Manual for Mental Disorders (DSM-IV-TR) diagnostic criteria for Autistic Disorder (AD), screened by the SCQ and confirmed by the ADI-R Exclusion Criteria: - Patient weighing < 13kg - Allergy to porcine products - Previous sensitization or allergy to trypsin, pancreatin, or pancrelipase - History of severe head trauma, as defined by loss of consciousness or hospitalization, skull fracture or stroke. - Seizure within the last year prior to enrollment, or the need for seizure medications either at present or in the past. - Evidence or history of severe, moderate or uncontrolled systemic disease - Ongoing dietary restriction for allergy or other reasons except nut allergies. Lactose free is allowable but not dairy free. - Inability to ingest the study drug / non-compliance with dosing schedule. - Inability to follow the prescribed dosing schedule. - Use of any stimulant or non-stimulant medication or medications given for attention deficit hyperactivity disorder (ADHD) must be discontinued 5 days prior to the initial randomized study period. - Subjects taking an selective serotonin reuptake inhibitor (SSRI) must be on a stable dose for a minimum of 30 days prior to entering the study. - History of premature birth <35 weeks gestation. - Prior history of stroke in utero or other in utero insult. |
Country | Name | City | State |
---|---|---|---|
United States | Lovelace Scientific Resources | Albuquerque | New Mexico |
United States | Detroit Clinical Research Center, P.C. | Bingham Farms | Michigan |
United States | Montefiore Med.Cneter, Autism & Obsessive Compulsive Spectrum Program | Bronx | New York |
United States | IMMUNOe Research Centers | Centennial | Colorado |
United States | Carolina Clinical Trials, Inc. | Charleston | South Carolina |
United States | University of Virginia, Dept. of Psychiatry and Neurobehavioral Sciences | Charlottesville | Virginia |
United States | Cleveland Clinic Autism Center | Cleveland | Ohio |
United States | Focus Center of Clinical Research | Clinton | Utah |
United States | Duke Center For Autism and Brain Development | Durham | North Carolina |
United States | Children'S Specialized Hospital | Egg Harbor Township | New Jersey |
United States | Neuroscience, Inc | Herndon | Virginia |
United States | University of Texas, Houston-Behavioral & Biomedical Sciences | Houston | Texas |
United States | Lake Charles Clinical Trials | Lake Charles | Louisiana |
United States | Arkansas Children'S Hosp. Research Institute (A.C.H.R.I.) | Little Rock | Arkansas |
United States | Vanderbilt Universtiy Med.Center-Treatment&Research Inst. For Asd | Nashville | Tennessee |
United States | Yale Child Study Center | New Haven | Connecticut |
United States | Research Institute of Deaconess Clinic | Newburgh | Indiana |
United States | Segal Institute For Clinical Research | North Miami | Florida |
United States | N.R.C. Research Institute | Orange | California |
United States | Advent Health -Lake Mary Pediatrics | Orange City | Florida |
United States | A.P.G. Research | Orlando | Florida |
United States | Southwest Autism Research & Resource Center (S.A.R.R.C.) | Phoenix | Arizona |
United States | Carilion Clinic-Virginia Tech, Carilion School of Medicine | Roanoke | Virginia |
United States | M.I.N.D. Institute (Univ.of California, Davis) | Sacramento | California |
United States | University of California (U.C.S.F.) | San Francisco | California |
United States | L.S.U. Health Sciences Center | Shreveport | Louisiana |
United States | Richmond Behavioral Associates | Staten Island | New York |
United States | Barbara Enright | Toms River | New Jersey |
United States | University of Arizona, Pediatrics Multidisciplinary Research Unit | Tucson | Arizona |
United States | Clinical Research Center of Nj | Voorhees | New Jersey |
United States | Omega Medical Research | Warwick | Rhode Island |
Lead Sponsor | Collaborator |
---|---|
Curemark |
United States,
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* Note: There are 28 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Aberrant Behavioral Checklist: Subscale of Irritability / Agitation (ABC-I) at fecal chymotrypsin (FCT) levels less than or equal to 12.6 | Change from Baseline to each post-baseline visit, through study completion Week 72. | ||
Secondary | Aberrant Behavior Checklist: Subscale of Lethargy / Social Withdrawal (ABC-L) at fecal chymotrypsin (FCT) levels less than or equal to 12.6 | Change from Baseline to each post-baseline visit, through study completion Week 72. |
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