Overview
Multisite 14-week prospective double-blind placebo controlled parallel-group randomized clinical trial with 14-week open-label extension at the end of double-blind treatment phase for placebo subjects. Eligible subjects will be randomized within each site in 2:1 ratio to receive either TB006 or placebo treatment.
Description
A key molecular mechanism implicated in ASD is immune dysregulation and unchecked neuroinflammation marked by increased microglial activation. Galectin-3 (Gal-3), a galactoside-binding lectin, is critical to activation of neuroinflammation resulting in the proliferation of microglia.7 Gal-3 has been shown to be elevated in individuals with ASD. To inhibit Gal-3's contribution to neuroinflammation, Truebinding has developed TB006, a neutralizing monoclonal antibody against Gal-3. Our overall hypothesis is that TB006 will significantly improve core and associated behavioral symptoms of ASD and be well tolerated with no significant adverse effects in adults with ASD.
Eligibility
Inclusion Criteria:
- Autism Spectrum Disorder as defined below by the ADOS or ADI-R.
- Between 18 and 35 years of age at baseline.
- English included in the languages in which the individual is being raised.
- Autism severity of moderate or higher (≥4) under the 7-item clinical global impression-severity scale.
- Ability to maintain all ongoing complementary, dietary, traditional, and behavioral treatments constant for the study period.
- Unchanged complementary, dietary, traditional, and behavioral treatments for two months prior to study entry.
- In males and females of childbearing age, two forms of birth control must be used unless they are not sexually active.
- A caretaker who will accompany the patient to all procedures and has adequate contact with the participant to complete caregiver questionnaires.
Exclusion Criteria:
- LGALS3 rs4644 single nucleotide polymorphism with two copies of the Variant-type allele.
- History of infusion reactions to immunoglobulin product.
- Significant self-abusive or violent behavior or evidence of suicidal ideation, plan or behavior.
- Severely affected as defined by CGI-Severity Standard Score = 7 (Extremely Ill).
- Severe prematurity (<34 weeks gestation) as determined by medical history.
- Current uncontrolled gastroesophageal disorders.
- Current or history of liver or kidney disease as determined by medical history and safety labs (See Laboratory Values Monitoring Plan for specific laboratory values).
- Genetic syndromes.
- Congenital brain malformations.
- Active Epilepsy Diagnosis (Epilepsy Diagnosis is defined as History of two or more unprovoked seizures; Patient with a history of epilepsy who have been off medication without seizures for more than two years do not qualify as active epilepsy).
- Any medical condition that the PI determines could jeopardize the safety of the study subject or compromise the integrity of the data.
- Significant negative reaction (i.e., fainting, vomiting, etc.) because of a previous blood draw.
- Failure to thrive or < 5%ile for Body Mass Index or weight at the time of screening.
- Concurrent treatment with drug that would significantly interact with the investigational product.
- Allergy or Sensitivity to ingredients in the investigational product or placebo.
- Evaluation with the NIH Toolbox or BOSCC within 3 months of entering the study.
- Planned evaluation with the NIH Toolbox or BOSCC during the study.
- Pregnancy
- Current DSM-5 diagnosis requiring alternative pharmacotherapy, e.g., Major Depression, Bipolar Disorder, a psychotic disorder (based on clinical assessment assisted by the Child and Adolescent Symptom Inventory).
- Refusal to comply with the use of birth control if sexually active.
- Abnormal vital signs (systolic blood pressure > 180 mmHg or < 90 mmHg; heart rate > 120 beats per minute or < 55 beats per minute; temperature > 101.0o F; oxygen saturation < 90%)
- Prolonged QTc (defined as > 450ms for males and >470ms for female) or any abnormalities felt by the investigator to be of concern.