Clinical trials: 16P11.2 Deletion Syndrome
16P11.2 Deletion Syndrome, 16p11.2 Duplications
Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight
Simons Searchlight is an observational, online, international research program for families with rare genetic variants that cause neurodevelopmental disorders and may be associated with autism.
- Conditions
- 16P11.2 Deletion Syndrome, 16p11.2 Duplications, 1Q21.1 Deletion, 1Q21.1 Microduplication Syndrome (Disorder)
- Trial name
- NCT01238250
- Where
- 2 sites in United States
- Volunteers
- 100,000 people
- Sponsor
- Simons Searchlight
16P11.2 Deletion Syndrome
Safety, Tolerability, and Efficacy of Arbaclofen in 16p11.2 Deletion
This Phase 2 study examines the safety, tolerability, and efficacy of arbaclofen in pediatric subjects with 16p11.2 deletion. Male or female subjects aged 5 to 17 years of age will be randomized to receive either placebo or…
- Trial name
- NCT04271332
- Testing
- Arbaclofen
- Where
- 4 sites in United States
- Volunteers
- 60 people
- Sponsor
- Clinical Research Associates, LLC