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Condition: Rare Neurodevelopmental Conditions Synced from ClinicalTrials.gov · July 29, 2026

Recruiting studies: Rare Neurodevelopmental Conditions

Studies currently listed as recruiting on the public registry for this search term. Each page explains the study in plain language, with locations and the study team's contact details. Clinicians: generate a printable list for your patient →

Group CBT in Adolescents With Fragile X Syndrome and in Adolescents With Autism Spectrum Disorder
NA · 1 location(s) · Bambino Gesù Hospital and Research Institute · NCT06677866Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome
Phase N/A · 1 location(s) · Boston Children's Hospital · NCT05528744Clinical Trial of the Dual Vector Base Editor for the Treatment of the CHD3-R1025W Mutation
EARLY_Phase 1 · 1 location(s) · Yongguo Yu · NCT06860672Safety, Tolerability, and Preliminary Effectiveness of CTH120 in Fragile X Syndrome
Phase 2 · 2 location(s) · Connecta Therapeutics, S.L. · NCT07654114Expanding NGS Data with Optical Genome Mapping (OGM)
NA · 1 location(s) · IRCCS Eugenio Medea · NCT06851377Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
Phase N/A · 2 location(s) · Sanford Health · NCT01793168Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Proje
Phase N/A · 1 location(s) · University of Missouri-Columbia · NCT07329257Genome Medical Sequencing for Gene Discovery
Phase N/A · 1 location(s) · National Human Genome Research Institute (NHGRI) · NCT01087320Transcriptomic Analysis of Fibroblasts and Blood in Patients With Rare Diseases
NA · 1 location(s) · Assistance Publique Hopitaux De Marseille · NCT07075107A Study of AAV9 Gene Therapy in Participants With Canavan Disease (CANaspire Clinical Trial)
Phase 1/Phase 2 · 4 location(s) · Aspa Therapeutics · NCT04998396Epilepsy Learning Healthcare System (ELHS)
Phase N/A · 13 location(s) · Epilepsy Foundation of America · NCT06265103Genetic of Intellectual Deficiency and Autism Spectrum Disorders (RaDiCo-GenIDA)
Phase N/A · 1 location(s) · Institut National de la Santé Et de la Recherche Médicale, F · NCT06871696Baker Gordon Syndrome Natural History Study
Phase N/A · 1 location(s) · University of Missouri-Columbia · NCT06399952
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.