1 recruiting. .
Follow Simons Searchlight: new trials by email
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight 16P11.2 Deletion Syndrome, 16p11.2 Duplications | Recruiting | Simons Searchlight | 100000 | 2010-10-01 | 2026-07-23 |
15q24 Microdeletion (1) · 16p11.2 Deletion Syndrome (1) · Chromosome 15q13.3 Microdeletion Syndrome (1) · Chromosome 17q21.31 Deletion Syndrome (1) · Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb (1) · Chromosome 1q21.1 Duplication Syndrome (1) · Chromosome 2q37 deletion syndrome (1) · Cornea Plana 1 (1) · Cri-du-Chat Syndrome (1) · Epileptic Encephalopathy, Early Infantile, 4 (1) · Hereditary Sensory and Autonomic Neuropathies (1) · Rhabdoid Tumor Predisposition Syndrome 2 (1)
United States (1)
Cora Taylor, PhD (1) · Wendy Chung, MD PhD (1)