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Intravenous Immunoglobulin for PANDAS

A Placebo-Controlled Trial of Intravenous Immunoglobulin (IVIG) for PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infections)

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01281969
Enrollment
48
Registered
2011-01-24
Start date
2011-01-31
Completion date
2018-08-13
Last updated
2020-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety Disorder, Autoimmune Disease, Children, Obsessive-Compulsive Disorder, PANDAS

Keywords

Placebo Controlled, Obsessive-Compulsive Disorder, Children and Adolescents, Intravenous Immunoglobulin, PANDAS

Brief summary

Background: \- Some children experience a sudden onset of symptoms similar to those found in obsessive-compulsive disorder that may be caused by the body s reaction to an infection with streptococcal bacteria, most commonly seen as strep throat or scarlet fever. When the body s immune system reacts against brain cells following a streptococcal infection, the condition is known as PANDAS (pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections). The immune system response can be inactivated by treatment with a drug known as intravenous immunoglobulin (IVIG). Because there is insufficient research on IVIG s effects on the immune system of children with PANDAS, including whether IVIG is helpful in treating obsessive-compulsive symptoms related to PANDAS, researchers are interested in examining whether IVIG is an appropriate treatment for PANDAS and its associated symptoms. Objectives: \- To test the safety and effectiveness of intravenous immunoglobulin for the treatment of obsessive-compulsive disorder in children with PANDAS (pediatric autoimmune neuropsychiatric disorder associated with streptococcal infection). Eligibility: \- Children between 4 and 12 years of age who have obsessive-compulsive disorder (with or without a tic disorder) with sudden onset of symptoms following Group A streptococcal bacterial infections. Design: * Participants will be screened by telephone to obtain medical history and other information, followed by in-person screening at the National Institutes of Health Clinical Center. * Participants will be admitted to the hospital to receive 2 days of infusions of either IVIG or a placebo. Frequent blood samples, imaging studies, and other tests will be performed during this visit. * Six weeks after the inpatient stay, participants will return for further blood samples and other tests. Participants who did not receive the study drug, or who received the drug but did not respond to the initial IVIG infusion, will have the option to receive IVIG at this time. * Followup visits will take place 3 months and 6 months after the first evaluation, followed by yearly follow-ups for 5 additional years.

Detailed description

Objective: This study is designed to test the safety and efficacy of intravenous immunoglobulin (IVIG) for the treatment of obsessive-compulsive disorder (OCD) symptoms in children with PANDAS (pediatric autoimmune neuropsychiatric disorder associated with streptococcal infection). Study Population: Thirty-two male and female children with severe obsessive-compulsive symptoms related to a new onset or first recurrence of symptoms consistent with the PANDAS subtype of OCD. Design: his is a multi-site double-blind placebo-controlled trial. Potential subjects will be screened in person at NIMH, and there will be remote video corroboration by a team of collaborators at Yale University. Eligible subjects will be admitted to the 1NW pediatrics inpatient unit at the Clinical Center for further assessment, randomization, and study drug administration according to protocol. Subjects who fail to improve 6 weeks after blinded IVIG/placebo administration (1.0 gm/kg/day of IVIG on two consecutive days; total dose 2.0 gm/kg) will be eligible to receive open-label IVIG. Outcome Measures: * Primary: Improvement in obsessions, compulsions, and other neuropsychiatric symptoms. * Exploratory: * Reduction of titers of cross-reactive antibodies (Abs) * Resolution of basal ganglia inflammation (as measured by pre-/post-changes in MRI volumetric scans and inflammatory sequences) * Normalization of selected serum and CSF cytokines

Interventions

DRUGGamunex Intravenous Immunoglobulin

2.0 gm/kg total, IV (in the vein), over 2 days

DRUGPlacebo

Normal saline, IV (in the vein), over 2 days

Sponsors

National Institute of Mental Health (NIMH)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
4 Years to 13 Years
Healthy volunteers
No

Inclusion criteria

* INCLUSION CRITERIA: Male and female children 4-13 years of age. Presence of (Diagnostic and Statistical Manual of Mental Disorders Fourth Edition, Text Revision) DSM-IV TR OCD with or without a tic disorder. Moderate or greater severity of symptoms, with a score of greater than or equal to 20 on the Children s Yale-Brown Obsessive-Compulsive Scale (CY-BOCS) and greater than or equal to 4 on the Clinical Global Impression Severity scale (CGI-S). The acute onset within the previous six months of symptoms in a child previously well, or the first acute recurrence within the previous six months, after a period of relatively complete remission of symptoms. The acuity of symptom onset/exacerbation is key and must be severe, dramatic in onset, and proceed from no/minimal symptoms to maximum severity within 24-48 hours. Symptom onset or first exacerbation preceded within four months by a GAS infection, as documented by positive throat culture, exposure to documented GAS infection (in a close contact, such as a sibling sharing a bedroom), and/or documented two-fold rise in one or more anti-GAS antibody titers such as anti-streptolysin O, anti-streptococcal DNAaseB, anti-carbohydrate antibodies and others. Onset/exacerbation of OCD is accompanied by at least three of the following 7 clinical signs and symptoms. The acuity of the comorbid symptoms must be similar to the OCD symptoms and occur in the same time interval. 1. Markedly increased level of anxiety, particularly new onset of separation anxiety. 2. Emotional lability, irritability, aggressive behavior and/or personality change. 3. Sudden difficulties with concentration or learning. 4. Developmental regression (baby-talk, temper tantrums; behaviors atypical for actual chronological age). 5. Sleep disorder (insomnia, night terrors, refusal to sleep alone). 6. Handwriting deterioration or other sign of motoric dysfunction (including new onset of motor hyperactivity, or presence of choreiform finger movements). 7. Urinary frequency or increased urge to urinate; daytime or night-time secondary enuresis.

Exclusion criteria

History of rheumatic fever, including Sydenham chorea (the neurologic manifestation). Presence of symptoms consistent with autism, schizophrenia, or other psychotic disorder (unless psychotic symptoms have onset coincident with the possible PANDAS and are attributed to OCD). Presence of a neurological disorder other than a tic disorder. IQ \<70. Child subjects need to be able to contribute meaningfully to baseline and follow-up ratings, to report adverse effects, and to assent to participation. Presence of serious or unstable medical illness or psychiatric or behavioral symptoms that would make participation unsafe or study procedures too difficult to tolerate. IgA deficiency (\<20mg/dL). Intravenous immunoglobulin may contain trace IgA, which may very rarely lead to life-threatening anaphylaxis in IgA-deficient participants with anti-IgA antibodies (Misbah 1993). Hyperviscosity syndromes, which can increase risks associated with IVIG administration. Need for live virus vaccine within six months after receiving IVIG (which may be 7.5 months from randomization) since IVIG can interfere with effectiveness of such vaccines. IVIG should not be administered sooner than two weeks after administration of a live virus vaccine, for the same reason. Taking nephrotoxic drugs. Every concomitant medication will be subject to scrutiny and possible consultation with pediatric safety monitors before randomization to study drug. See below as well. Recent (less than eight weeks) initiation of cognitive-behavior therapy (CBT). Recent (less than eight weeks) initiation or change in dosage of psychotropic medication for OCD or tic disorder (e.g., serotonin reuptake inhibitors for OCD, alpha-2 agonists or antipsychotics for tic disorders).

Design outcomes

Primary

MeasureTime frameDescription
Children's Yale-Brown Obsessive Compulsive Scale Total Score6 weeksActive IVIG will be significantly superior to sham IVIG in reducing OC symptoms and providing global relief of neuropsychiatric symptomatology. Total score is reported as the sum of all items and has a range of 0-40. Higher scores indicate more severe symptoms.

Secondary

MeasureTime frameDescription
Clinical Global Impressions Improvement6 weeks1=very much improved, 2=much improved, 3=slightly improved, 4=no change, 5=slightly worse, 6=much worse, 7=very much worse
Clinical Responder to Treatment6 weeksDefined as a CGI-I score of 1 or 2 (much or very much improved) and a decrease in CY-BOCS of at least 30%
The Degree of Treatment Response is Expected to Correlate With the Percentage Reduction in Antinuclear Antibody Titers Following IVIG Administration.BaselineNon-zero values of antinuclear antibodies are considered positive and reflective of an ongoing immune response in the individual. First, the number of participants who were classified at baseline as having positive antinuclear antibodies was calculated (see outcome measure data table, which states the number (AKA count) of participants who had positive antinuclear antibodies at baseline). We hypothesized that improvement in the ongoing immune response, and therefore a reduction in antinuclear antibody titers, would mediate the effect of IVIG on OCD symptom improvement. However, because very few participants were classified as positive at baseline, it was not appropriate to pursue the original question of whether a decline in antinuclear antibodies (i.e., from positive to negative) was related to symptom improvement.
The Degree of Treatment Response is Also Expected to Correlate With Decreased Inflammation in Specific Regions of the Brain, as Demonstrated by Changes on MRI3 Months

Countries

United States

Participant flow

Participants by arm

ArmCount
IVIG
Gamunex Intravenous Immunoglobulin: 2.0 gm/kg total, IV (in the vein), over 2 days
17
Placebo
Placebo: Normal saline, IV (in the vein), over 2 days
18
Total35

Withdrawals & dropouts

PeriodReasonFG000FG001FG002
Overall StudyAE during LP prior to IVIG admin103
Overall Studynot randomized, child consent not given002
Overall Studynot randomized didn't meet criteria007

Baseline characteristics

CharacteristicIVIGPlaceboTotal
Age, Continuous8.99 years
STANDARD_DEVIATION 2.37
9.61 years
STANDARD_DEVIATION 2.32
9.30 years
STANDARD_DEVIATION 2.32
Children's Yale-Brown Obsessive Compulsive Scale Total26.47 units on a scale
STANDARD_DEVIATION 5.14
28.78 units on a scale
STANDARD_DEVIATION 3.98
27.65 units on a scale
STANDARD_DEVIATION 4.66
Clinical Global Impressions Severity
Extreme (7)
0 participants2 participants2 participants
Clinical Global Impressions Severity
Marked (5)
8 participants9 participants17 participants
Clinical Global Impressions Severity
Moderate (4)
2 participants3 participants5 participants
Clinical Global Impressions Severity
Severe (6)
7 participants4 participants11 participants
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants1 Participants2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
16 Participants17 Participants33 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants0 Participants1 Participants
Race (NIH/OMB)
Asian
1 Participants0 Participants1 Participants
Race (NIH/OMB)
Black or African American
1 Participants0 Participants1 Participants
Race (NIH/OMB)
More than one race
0 Participants2 Participants2 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
14 Participants16 Participants30 Participants
Region of Enrollment
United States
17 participants18 participants35 participants
Sex: Female, Male
Female
5 Participants7 Participants12 Participants
Sex: Female, Male
Male
12 Participants11 Participants23 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
17 / 175 / 18
serious
Total, serious adverse events
0 / 170 / 18

Outcome results

Primary

Children's Yale-Brown Obsessive Compulsive Scale Total Score

Active IVIG will be significantly superior to sham IVIG in reducing OC symptoms and providing global relief of neuropsychiatric symptomatology. Total score is reported as the sum of all items and has a range of 0-40. Higher scores indicate more severe symptoms.

Time frame: 6 weeks

ArmMeasureValue (MEAN)Dispersion
Group AChildren's Yale-Brown Obsessive Compulsive Scale Total Score20.59 units on a scaleStandard Deviation 10.12
Group BChildren's Yale-Brown Obsessive Compulsive Scale Total Score25.67 units on a scaleStandard Deviation 8.65
Comparison: Analysis of covariance model controlling for baseline scores. A priori power calculations based on the Perlmutter et al. study (IVIG effect size 1.2) suggested that a sample size of 16 per group would be sufficient to detect an effect size of 1.0 with 80% power.p-value: 0.4495% CI: [-7.1, 3.15]ANCOVA
Secondary

Clinical Global Impressions Improvement

1=very much improved, 2=much improved, 3=slightly improved, 4=no change, 5=slightly worse, 6=much worse, 7=very much worse

Time frame: 6 weeks

ArmMeasureValue (MEAN)Dispersion
Group AClinical Global Impressions Improvement2.88 units on a scaleStandard Deviation 1.2
Group BClinical Global Impressions Improvement3.53 units on a scaleStandard Deviation 1.62
Comparison: The Wilcoxon two-sample test was used to compare CGI-Improvement ratings (an ordinal variable) at week 6. Power calculation was based on CYBOCS as primary outcome.p-value: 0.12Wilcoxon (Mann-Whitney)
Secondary

Clinical Responder to Treatment

Defined as a CGI-I score of 1 or 2 (much or very much improved) and a decrease in CY-BOCS of at least 30%

Time frame: 6 weeks

ArmMeasureValue (NUMBER)
Group AClinical Responder to Treatment6 participants
Group BClinical Responder to Treatment4 participants
Comparison: Chi-squared test was used to compare distribution of responders by randomization group. Power calculation was based on CY-BOCS (primary outcome).p-value: 0.4Chi-squared
Secondary

The Degree of Treatment Response is Also Expected to Correlate With Decreased Inflammation in Specific Regions of the Brain, as Demonstrated by Changes on MRI

Time frame: 3 Months

Secondary

The Degree of Treatment Response is Expected to Correlate With the Percentage Reduction in Antinuclear Antibody Titers Following IVIG Administration.

Non-zero values of antinuclear antibodies are considered positive and reflective of an ongoing immune response in the individual. First, the number of participants who were classified at baseline as having positive antinuclear antibodies was calculated (see outcome measure data table, which states the number (AKA count) of participants who had positive antinuclear antibodies at baseline). We hypothesized that improvement in the ongoing immune response, and therefore a reduction in antinuclear antibody titers, would mediate the effect of IVIG on OCD symptom improvement. However, because very few participants were classified as positive at baseline, it was not appropriate to pursue the original question of whether a decline in antinuclear antibodies (i.e., from positive to negative) was related to symptom improvement.

Time frame: Baseline

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Group AThe Degree of Treatment Response is Expected to Correlate With the Percentage Reduction in Antinuclear Antibody Titers Following IVIG Administration.8 Participants
Group BThe Degree of Treatment Response is Expected to Correlate With the Percentage Reduction in Antinuclear Antibody Titers Following IVIG Administration.5 Participants

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026