There are currently 3 active clinical trials seeking participants for Angelman Syndrome research studies. The states with the highest number of trials for Angelman Syndrome participants are California, Massachusetts, New York and Illinois.
REVEAL: A Phase 3 Study of ION582 in Angelman Syndrome
Recruiting
The purpose of this study is to evaluate the efficacy and safety of ION582 in children and adults with Angelman syndrome caused by a deletion or mutation of the UBE3A gene.
Gender:
ALL
Ages:
Between 2 years and 50 years
Trial Updated:
08/05/2025
Locations: Rady Children's Hospital, San Diego, California +2 locations
Conditions: Angelman Syndrome
Angelman Syndrome Natural History Study
Recruiting
The goal of this study is to conduct a prospective, longitudinal natural history study of children and adults with Angelman Syndrome using investigator-observed and parent-reported outcome measures to obtain data that will be useful for future clinical trials.
Gender:
ALL
Ages:
All
Trial Updated:
03/30/2025
Locations: Cedars-Sinai Guerin Children's, Los Angeles, California +10 locations
Conditions: Angelman Syndrome
Web Intervention for Parents of Youth With Genetic Syndromes (WINGS)
Recruiting
The purpose of this study is to evaluate the effectiveness of an adapted, telehealth functional behavioral therapy (FBTsIDD) specifically focused on promoting appropriate communication and behavioral strategies in individuals with syndromic intellectual and developmental disorders. Participants will be asked to complete virtual study assessments at intake and then on a monthly basis for the duration of 3-6 months. In addition, participants will attend weekly or biweekly virtual intervention vis... Read More
Gender:
ALL
Ages:
Between 2 years and 12 years
Trial Updated:
01/29/2025
Locations: Autism Assessment Research Treatment and Services (AARTS) Center at Rush University Medical Center, Chicago, Illinois
Conditions: Telomeric 22Q13 Monosomy Syndrome, Tuberous Sclerosis, Hamartoma Syndrome, Multiple, Fragile X Syndrome, Angelman Syndrome, Rett Syndrome, Chromosome 15Q, Partial Deletion, Creatine Deficiency, X-linked