Xolair Interventional Study in ASD Patients With Comorbid Atopy
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Beth Israel Deaconess Medical Center
- Study ID
- NCT04535817
- Phase
- PHASE1
- Status
- Withdrawn
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 30 Years
- Healthy Volunteers
- Not accepted
Interventions
- Omalizumab Injection [Xolair] — DRUG300mg via 2 subcutaneous injections every 4 weeks
Study Details
Following the publication of two case studies that reported behavioral benefit in ASD patients treated with omalizumab, the investigators will conduct a pilot trial to test the proof-of-concept efficacy of omalizumab in ASD patients with comorbid atopic disease. Investigators will evaluate behavioral improvement using three questionnaires. Investigators will also perform fMRI on all subjects and obtain serum samples for quantification of immunological biomarkers. If the trial is conclusive, the investigators will conduct a larger-scale, randomized-controlled trial to further understand the pathology of allergy in this subpopulation of ASD patients and the efficacy of this intervention.
Key Dates
- Start date
- Jan 1, 2021
- Status verified
- Aug 2021
- Primary completion
- Jan 1, 2022
- Completion
- Jan 1, 2022
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment GroupSubjects will receive subcutaneous treatment of 300mg of omalizumab during the 24-week treatment period. One injection will be administered every 4 weeks.
Primary Outcome Measure
Change from Baseline to Week 12 in Social Responsiveness Scale (SRS) Edition 2 [ Time Frame: Baseline and Week 12 ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Beth Israel Deaconess Medical Center | Boston | Massachusetts | 02215 | - |
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