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Clinical Trial Summary

This study will evaluate the use of intravenous immunoglobulins (IVIG) at a dose of 1g/Kg/body weight given every three weeks for 6 infusions in pediatric subjects ages 4 - 16 years with moderate to severe PANS. The study will compare biomarkers and behavioral scales before treatment, after the last infusion, 2 months, and at a minimum 6 months post-treatment.


Clinical Trial Description

IVIG at an immunomodulatory dose of 1 g/Kg body weight has been known to induce suppression of systemic inflammation and has been used in the treatment of autoimmune diseases. It has been proven beneficial in inflammatory conditions affecting the nervous system. ;


Study Design


Related Conditions & MeSH terms

  • Pediatric Acute-Onset Neuropsychiatric Syndrome
  • Pediatric Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infections
  • Streptococcal Infections
  • Syndrome

NCT number NCT03348618
Study type Interventional
Source IMMUNOe Research Centers
Contact
Status Active, not recruiting
Phase Phase 4
Start date November 24, 2017
Completion date March 2020

See also
  Status Clinical Trial Phase
Recruiting NCT02889016 - Neurobiologic, Immunologic, and Rheumatologic Markers in Youth With PANS N/A
Active, not recruiting NCT04508530 - Phase III Study To Compare The Effect of Panzyga Versus Placebo in Patients With Pediatric Acute-onset Neuropsychiatric Syndrome (PANS/PANDAS) Phase 3
Recruiting NCT06213090 - Patterns of Neurodevelopmental Disorders