Sulforaphane in a New Jersey (NJ) Population of Individuals With Autism
Primary Purpose
Autism, Autistic Disorder, Autism Spectrum Disorder
Status
Active
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Sulforaphane
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Autism
Eligibility Criteria
Inclusion Criteria:
- Autistic disorder diagnosis.
- Age between 13-30 years.
- Male gender.
Exclusion Criteria:
- Absence of a parent or legal guardian and consent,
- Those that can not or will not complete all visits and adherence to study regimen.
- Seizure within 2 years of screening,
- Impaired renal function (serum creatinine> 1.2 mg/dl).
- Impaired hepatic function (> 2x upper limit of normal).
- Impaired thyroid function (TSH outside normal limits).
- Current infection or treatment with antibiotics.
- Chronic medical disorder (e.g., cardiovascular disease, stroke or diabetes) or major surgery within 3 months prior to enrollment.
- Less than 13 years or more than 30 years of age.
- Female gender.
- A diagnosis of autism spectrum disorder other than autistic disorder, for example, Asperger, Pervasive Developmental Disorder Not Otherwise Specified (PDD-NOS) etc.
Sites / Locations
- Rutgers University - Staged Research Building
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Placebo
Sulforaphane
Arm Description
About 15 subjects will be randomized into this arm, receiving pills with an inactive placebo.
About 30 subjects will be randomized into this arm, receiving pills with glucoraphanin rich broccoli seed powder containing active myrosinase resulting in sulforaphane once ingested Doses will be weight dependent with each pill resulting in ~ 50 µmol sulforaphane. Body weight Dose of sulforaphane 34 kg ~ 50 µmol 68 kg ~ 100 µmol 102 kg ~ 150 µmol
Outcomes
Primary Outcome Measures
Change in Aberrant Behavior Checklist (ABC) scores.
Change in Social Responsiveness Scale (SRS) scores.
Clinical Global Impression Severity Scale (CGI-S).
Clinical Global Impression Improvement Scale (CGI-I) to measure change from baseline CGI-S scores.
Secondary Outcome Measures
Liver Function Tests as a screen for entry into the study and a monitor of potential change/adverse events due to treatment.
Renal Function Tests as a screen for entry into the study and a monitor of potential change/adverse events due to treatment.
Thyroid Stimulating Hormone (TSH) as a screen for entry into the study and a monitor of potential change/adverse events due to treatment.
Full Information
NCT ID
NCT02677051
First Posted
January 28, 2016
Last Updated
August 18, 2023
Sponsor
Rutgers, The State University of New Jersey
Collaborators
Rowan University
1. Study Identification
Unique Protocol Identification Number
NCT02677051
Brief Title
Sulforaphane in a New Jersey (NJ) Population of Individuals With Autism
Official Title
Sulforaphane in Autism: A Treatment Trial to Confirm Phenotypic Improvement With Sulforaphane Treatment in a New Jersey (NJ) Population of Individuals With Autism
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 2016 (undefined)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
July 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rutgers, The State University of New Jersey
Collaborators
Rowan University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is a double blind treatment trial that will test if sulforaphane improves core symptoms in autism. The investigators expect to see clinical improvement in some of these areas. Sulforaphanes come from eating certain vegetables such as broccoli. The investigators will be using a preparation that gives specific and reproducible amounts. The investigators will also test specific chemicals and genes needed for sulforaphane usage to try to understand differences in response.
Detailed Description
This study is a double blind randomized treatment trial that will test if sulforaphane improves core symptoms in autism. It is designed to try to replicate a previous trial (ClinicalTrials.gov Identifier NCT01474993) which reported that the isothiocyanate, sulforaphane treatment led to improvement by multiple metrics. Significant improvement was seen in behavior as measured by the Aberrant Behavioral Checklist (ABC) and by the Social Responsiveness Scale (SRS). In addition a significantly greater number of participants receiving sulforaphane had improvement in social interaction, abnormal behavior, and verbal communication as per the Clinical Global Impression (CGI). In addition The investigators will attempt to account for some variability in response to sulforaphane treatment by testing alleles of genes that are relevant in sulforaphane metabolism. The investigators will also measure glutathione levels, which are also important in sulforaphane metabolism and are in part regulated by sulforaphane..
Sulforaphane is the most potent naturally occurring inducer of mammalian cytoprotective enzymes known. Therapeutic potential is based at least in part on their ability to up-regulate genes responsible for alleviation of oxidative stress and to regulate both the immune system and the inflammatory response
40 Males with autistic disorder will be randomly selected to receive either sulforaphane or placebo. Seven visits are required by the subjects including enrollment ,screening, baseline, weeks 4, 10 and 18 and a follow up visit at seek 22.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autism, Autistic Disorder, Autism Spectrum Disorder, Autistic Behavior
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
48 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
About 15 subjects will be randomized into this arm, receiving pills with an inactive placebo.
Arm Title
Sulforaphane
Arm Type
Experimental
Arm Description
About 30 subjects will be randomized into this arm, receiving pills with glucoraphanin rich broccoli seed powder containing active myrosinase resulting in sulforaphane once ingested Doses will be weight dependent with each pill resulting in ~ 50 µmol sulforaphane.
Body weight Dose of sulforaphane 34 kg ~ 50 µmol 68 kg ~ 100 µmol 102 kg ~ 150 µmol
Intervention Type
Drug
Intervention Name(s)
Sulforaphane
Other Intervention Name(s)
Avmacol
Intervention Description
Sulforaphane (1-isothiocyanato-4R- (methylsulfinyl)butane) is an isothiocyanate derived from the action of the plant enzyme myrosinase on glucosinolates including glucoraphanin and comes from consumption of many cruciferous vegetables.
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Change in Aberrant Behavior Checklist (ABC) scores.
Time Frame
Baseline, week 4, week 10, week 18 and week 22.
Title
Change in Social Responsiveness Scale (SRS) scores.
Time Frame
Baseline, week 4, week 10, week 18 and week 22.
Title
Clinical Global Impression Severity Scale (CGI-S).
Time Frame
Baseline
Title
Clinical Global Impression Improvement Scale (CGI-I) to measure change from baseline CGI-S scores.
Time Frame
Week 4, week 10, week 18 and week 22.
Secondary Outcome Measure Information:
Title
Liver Function Tests as a screen for entry into the study and a monitor of potential change/adverse events due to treatment.
Time Frame
Baseline, week 4, week 18 and week 22.
Title
Renal Function Tests as a screen for entry into the study and a monitor of potential change/adverse events due to treatment.
Time Frame
Baseline, week 4, week 18 and week 22.
Title
Thyroid Stimulating Hormone (TSH) as a screen for entry into the study and a monitor of potential change/adverse events due to treatment.
Time Frame
Baseline, week 4, week 18 and week 22.
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
13 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Autistic disorder diagnosis.
Age between 13-30 years.
Male gender.
Exclusion Criteria:
Absence of a parent or legal guardian and consent,
Those that can not or will not complete all visits and adherence to study regimen.
Seizure within 2 years of screening,
Impaired renal function (serum creatinine> 1.2 mg/dl).
Impaired hepatic function (> 2x upper limit of normal).
Impaired thyroid function (TSH outside normal limits).
Current infection or treatment with antibiotics.
Chronic medical disorder (e.g., cardiovascular disease, stroke or diabetes) or major surgery within 3 months prior to enrollment.
Less than 13 years or more than 30 years of age.
Female gender.
A diagnosis of autism spectrum disorder other than autistic disorder, for example, Asperger, Pervasive Developmental Disorder Not Otherwise Specified (PDD-NOS) etc.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven Buyske
Organizational Affiliation
Rutgers, The State University of NJ
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rutgers University - Staged Research Building
City
Piscataway
State/Province
New Jersey
ZIP/Postal Code
08854
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
25313065
Citation
Singh K, Connors SL, Macklin EA, Smith KD, Fahey JW, Talalay P, Zimmerman AW. Sulforaphane treatment of autism spectrum disorder (ASD). Proc Natl Acad Sci U S A. 2014 Oct 28;111(43):15550-5. doi: 10.1073/pnas.1416940111. Epub 2014 Oct 13.
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Sulforaphane in a New Jersey (NJ) Population of Individuals With Autism
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