Phase
Condition
Asperger's Disorder
Autism Spectrum Disorder (Asd)
Autism
Treatment
N/AClinical Study ID
Ages 18-35 Male Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion criteria for participants with ASD
Male with a diagnosis of ASD as defined by DSM-5, confirmed by clinical evaluation and ADOS-2.
Age 18-35 years inclusive
IQ estimate of >70 on VIQ or PIQ
Capacity to consent to research
Ability to comply with all protocol procedures and assessments
Availability of an informant willing to provide information regarding subject behavior and health status (Note: Informant role requires a responsible adult with close, ongoing contact and knowledge of the subject; parent/caregiver acceptable, but not necessary for role)
Exclusion criteria for participants with ASD
Evidence of current nicotine, drug, or alcohol abuse or dependence
Presence of a chronic medical condition which would potentially influence the assessment of TSPO binding, or interact with study medication (eg. hepatic, neurologic, renal disease) to increase risk to the subject
Presence of severe behavioral disturbance likely to require initiation of treatment during the course of the protocol
Clinical judgment of the study physician of inability to perform the requirements of the study
Current or recent (past 30 days) treatment with minocycline or related compounds, immunosuppressives, or benzodiazepines
Homozygous genotype for minor allele of rs6971
History of recent febrile illness in past 30 days
History of allergic reactions to tetracycline antibiotics
Concomitant medication treatment not stable for the 4 weeks prior to study entry or anticipated to change
Current prescribed medication likely to confound assessment of TSPO binding
Inclusion criteria for healthy volunteer participants
Male in good general health, confirmed by clinical evaluation
Age 18-35 years inclusive
IQ estimate of >70 on VIQ or PIQ
Ability to comply with all protocol procedures and assessments
Exclusion criteria for healthy volunteer participants
Diagnosis of an autism spectrum disorder (ASD)
Evidence of current nicotine, drug, or alcohol abuse or dependence
Presence of a chronic medical condition which would potentially influence the assessment of TSPO binding, or interact with study medication (eg. hepatic, neurologic, renal disease) to increase risk to the subject
Presence of current or lifetime severe psychopathology potentially confounding assessment of TSPO binding (psychosis, severe depression, bipolar disorder, Obsessive-Compulsive Disorder)
Current prescribed medication likely to confound assessment of TSPO binding
Clinical judgment of the study physician of inability to perform the requirements of the study
Current or recent (past 30 days) treatment with minocycline or related compounds, immunosuppressives, benzodiazepines, or psychotropic medications likely to confound assessment of TSPO binding
Homozygous genotype for minor allele of rs6971
SRS-2 T-score score of >59
History of recent febrile illness in past 30 days
Study Design
Connect with a study center
UCLA
Los Angeles, California 90095
United StatesSite Not Available

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