Measuring Brain Inflammation in Autism

Autism Spectrum Disorder Clinical Trial

Official title:

Targeting Microglial Activation for Treatment of Autism Spectrum Disorder (ASD): A Proof-of-Concept, Target-Engagement Study

Clinical Trial Details — Status: Suspended

Administrative data

• NCT number: NCT03117530
• Other study ID #: 16-001784
• Status: Suspended
• Phase: Phase 1
• Start date: April 11, 2017
• Est. completion date: December 2022

Study information

• Verified date: August 2020
• Source: University of California, Los Angeles
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Autism spectrum disorders (ASD) are highly disabling, persistent neurodevelopmental disorders. There are no available treatments for core symptoms of ASD or biologically-based clinical biomarkers. Emerging evidence indicates that levels of brain inflammation are increased in ASD. In particular, recent work implicates hyperactivity of microglial cells, the resident immune cells of the brain. However, the functional consequences of microglial activation remain unknown. This study will measure microglial activation in ASD using positron emission tomography (PET) brain imaging. Adult males with ASD (n=15) and healthy controls (n=15) will be recruited for this study and undergo comprehensive clinical and behavioral baseline assessment. All subjects will then undergo baseline PET imaging using a radiotracer that labels activated microglia. Subjects with ASD will then undergo 12-week open label treatment with minocycline, an FDA-approved antibiotic thought to block microglial activation. PET imaging will be repeated at 12 weeks to confirm target engagement. A subset of control subjects will also undergo repeat PET imaging to determine test-retest reliability. During minocycline treatment, ASD subjects will be evaluated every 2 weeks for safety, clinical impression, behavioral functioning, and measures of cognition. Results will provide important information regarding the relationship between levels of brain inflammation, cognitive and behavioral function in ASD.

Recruitment information / eligibility

• Status: Suspended
• Enrollment: 30
• Est. completion date: December 2022
• Est. primary completion date: December 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 35 Years

Eligibility

Inclusion criteria for participants with ASD

1. Male with a diagnosis of ASD as defined by DSM-5, confirmed by clinical evaluation and ADOS-2.

2. Age 18-35 years inclusive

3. IQ estimate of >70 on VIQ or PIQ

4. Capacity to consent to research

5. Ability to comply with all protocol procedures and assessments

6. 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

1. Evidence of current nicotine, drug, or alcohol abuse or dependence

2. 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

3. Presence of severe behavioral disturbance likely to require initiation of treatment during the course of the protocol

4. Clinical judgment of the study physician of inability to perform the requirements of the study

5. Current or recent (past 30 days) treatment with minocycline or related compounds, immunosuppressives, or benzodiazepines

6. Homozygous genotype for minor allele of rs6971

7. History of recent febrile illness in past 30 days

8. History of allergic reactions to tetracycline antibiotics

9. Concomitant medication treatment not stable for the 4 weeks prior to study entry or anticipated to change

10. Current prescribed medication likely to confound assessment of TSPO binding

Inclusion criteria for healthy volunteer participants

1. Male in good general health, confirmed by clinical evaluation

2. Age 18-35 years inclusive

3. IQ estimate of >70 on VIQ or PIQ

4. Ability to comply with all protocol procedures and assessments

Exclusion criteria for healthy volunteer participants

1. Diagnosis of an autism spectrum disorder (ASD)

2. Evidence of current nicotine, drug, or alcohol abuse or dependence

3. 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

4. Presence of current or lifetime severe psychopathology potentially confounding assessment of TSPO binding (psychosis, severe depression, bipolar disorder, Obsessive-Compulsive Disorder)

5. Current prescribed medication likely to confound assessment of TSPO binding

6. Clinical judgment of the study physician of inability to perform the requirements of the study

7. Current or recent (past 30 days) treatment with minocycline or related compounds, immunosuppressives, benzodiazepines, or psychotropic medications likely to confound assessment of TSPO binding

8. Homozygous genotype for minor allele of rs6971

9. SRS-2 T-score score of >59

10. History of recent febrile illness in past 30 days

Related Conditions & MeSH terms

• Autism Spectrum Disorder
• Autistic Disorder

Intervention

Drug:
• Minocycline
Following initial baseline PET-CT imaging and clinical evaluation, adults with ASD will undergo a 12- week open-label treatment trial of minocycline to be conducted at UCLA under supervision of the UCLA IRB. During weeks 1-6, ASD subjects will be treated with 50 mg minocycline twice daily (low dose). From weeks 7-12, dosing will be increased to 100mg twice daily (typical clinical dosage). Every two weeks during this phase, a treating clinician will measure vital signs, assess safety, record adverse effects, and monitor compliance. Compliance will be obtained as an index of tolerability and will assessed through weekly medication diaries and pill counts.

Locations

Country	Name	City	State
United States	UCLA	Los Angeles	California

Sponsors (1)

Lead Sponsor	Collaborator
University of California, Los Angeles

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change in clinician-rated global improvement as measured by CGI		Data will be collected at Screening Visit #1 (between days -28 and 0 before intervention) and at visits during Weeks 6 and 12 of intervention
Other	Change in self-reported symptoms of ASD with minocycline treatment as measured by SRS-2		Data will be collected at Screening Visit #1 (between days -28 and 0 before intervention) and at visits during Weeks 6 and 12 of intervention
Other	Change in informant-reported symptoms of ASD with minocycline treatment as measured by ABC-CV		Data will be collected at Screening Visit #1 (between days -28 and 0 before intervention) and at visits during Weeks 6 and 12 of intervention
Primary	Evaluate differences in CNS microglial activation in adults with ASD versus healthy volunteers via in vivo CNS binding of [11C]-DAA1106		Data will be collected at PET scan #1, which will take place during screening (Days -28 to 0) for the study
Primary	Evaluate the effect of 12-weeks of minocycline exposure on CNS microglial activation in adults with ASD by measuring change in [11C]-DAA1106 binding pre- and post- treatment		Data will be collected at PET scan #1 (between days -28 and 0 before intervention) and at PET scan #2 during Week 12 of intervention
Secondary	Effect of minocycline exposure on cognition across seven cognitive domains before and after low dose intervention and regular dose intervention as measured by MCCB (MATRICS Consensus Cognitive Battery) subdomain scores		Data will be collected at baseline and during Weeks 6 and 12 of intervention
Secondary	Effect of minocycline exposure on self-rated anxiety and emotion regulation as measured by ADAMS (Anxiety and Depression Mood Scale)		Data will be collected at baseline and during Weeks 6 and 12 of intervention
Secondary	Effect of minocycline exposure on peripheral inflammatory cytokine profiles as measured by DNA and RNA expression in blood samples		Data will be collected PET #1 (week 0) and at PET scan #2 (Week 12)