Chromosome 2q37 deletion syndrome: Clinical Trials

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Follow Chromosome 2q37 deletion syndrome: new trials by email Literature Review of Chromosome 2q37 deletion syndrome trials Research Report on Chromosome 2q37 deletion syndrome

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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

Narrower conditions

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)  ·  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)

Broader conditions

Abnormalities, Multiple (1)  ·  Chromosome Disorders (1)  ·  Congenital Abnormalities (1)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (1)  ·  Genetic Diseases, Inborn (1)  ·  Heredodegenerative Disorders, Nervous System (1)  ·  Intellectual Disability (1)  ·  Nervous System Diseases (1)  ·  Nervous System Malformations (1)  ·  Neurobehavioral Manifestations (1)  ·  Neurodegenerative Diseases (1)  ·  Neurologic Manifestations (1)  ·  Neuromuscular Diseases (1)  ·  Peripheral Nervous System Diseases (1)  ·  Polyneuropathies (1)

Sponsors

Simons Searchlight (1)

Countries

United States (1)

Top investigators

Cora Taylor, PhD (1)  ·  Wendy Chung, MD PhD (1)