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Идёт набор NCT06500637

TB006 for Autism Spectrum Disorder

Фаза II С лечением Autism Spectrum Disorder

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: TB006.
Кому может быть актуально
Состояния в реестре: Autism Spectrum Disorder. Базовые параметры: 18 лет — 35 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

A Multi-center Double Blind Placebo Controlled Study to Assess the Safety and Efficacy of TB006 for Improving Core Symptoms in Adults With Autism Spectrum Disorder

Обзор

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.

Подробное описание

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.

Вмешательства

  • Препарат TB006
    TB006 is a humanized immunoglobulin G4 (IgG4) (S228P) type monoclonal antibody that is highly specific and has a high affinity to human Galectin-3 (hGal-3).

Первичные конечные точки

  • Childhood Autism Rating Scores (CARS) [Срок оценки: Baseline, Week 8 and Week 14]
Вторичные конечные точки (7)
  • NIH Toolbox [Срок оценки: Baseline and Week 14]
  • Clinical Global Impression Scale (CGI) [Срок оценки: Baseline, Week 8 and Week 14]
  • Social Responsiveness Scale (SRS) [Срок оценки: Baseline, Week 8, Week 12 and Week 14]
  • Aberrant Behavior Checklist (ABC) [Срок оценки: Screening, Weeks 4, 8, 12 and 14]
  • Major Parental Concerns [Срок оценки: Baseline, Week 8, Week 12 and Week 14]
  • Ohio State University Clinical Impressions Scale [Срок оценки: Baseline and Week 14]
  • Vineland Adaptive Behavior Scale [Срок оценки: Baseline, Week 8 and Week 14]

Критерии участия

Критерии включения

  • 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.

Критерии исключения

  • 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.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Четверное слепое
Основная цель
Лечение

Центры проведения

США · 2 центра
  • Rossignol Medical Center — Phoenix
  • Rossignol Medical Center — Aliso Viejo

Публикации

  • Rodriguez JI, Kern JK. Evidence of microglial activation in autism and its possible role in brain underconnectivity. Neuron Glia Biol. 2011 May;7(2-4):205-13. doi: 10.1017/S1740925X12000142. Epub 2012 Jul 6. PMID 22874006
  • Garcia-Revilla J, Boza-Serrano A, Espinosa-Oliva AM, Soto MS, Deierborg T, Ruiz R, de Pablos RM, Burguillos MA, Venero JL. Galectin-3, a rising star in modulating microglia activation under conditions of neurodegeneration. Cell Death Dis. 2022 Jul 20;13(7):628. doi: 10.1038/s41419-022-05058-3. PMID 35859075
  • Wang X, Zhang S, Lin F, Chu W, Yue S. Elevated Galectin-3 Levels in the Serum of Patients With Alzheimer's Disease. Am J Alzheimers Dis Other Demen. 2015 Dec;30(8):729-32. doi: 10.1177/1533317513495107. Epub 2013 Jul 2. PMID 23823143
  • Artik A, Kocaman O, Kara H, Tuncer SC. Galectin-3 levels in school aged children with autism spectrum disorder. Int J Dev Disabil. 2022 Dec 1;69(5):757-761. doi: 10.1080/20473869.2022.2150035. eCollection 2023. PMID 37547549

Идентификаторы

NCT: NCT06500637 · TB-RMC

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗