corpus callosum, agenesis of
corpus callosum, agenesis of
Explore linked clinical trials. Standard reference: MONDO:00090224 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Brain Development Research Program | Aicardi syndrome, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Malformations of Cortical Development, Group III, Neurobehavioral Manifestations, Neurologic Manifestations, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, X-linked disease, autism, autism spectrum disorder, brain disorder, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, corpus callosum, agenesis of, epilepsy, eye disorder, hereditary disease, intellectual disability, nervous system disorder, neurodevelopmental disorder, pervasive developmental disorder, polymicrogyria, psychiatric disorder | Recruiting | Not stated | 2026-08-17 | NCT00305305 | |
| Study of Selected X-Linked Disorders: Aicardi Syndrome | Aicardi syndrome, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, X-linked disease, brain disorder, central nervous system disorder, central nervous system malformation, corpus callosum, agenesis of, eye disorder, hereditary disease, nervous system disorder, neurodevelopmental disorder, psychiatric disorder | Recruiting | Not stated | 2026-05-05 | NCT00697411 | |
| Bioengineered Penile Tissue Constructs for Irreversibly Damaged Penile Corpora | Accidental Injuries, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corpus Callosum Malformation, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Genital Diseases, Inflammation, Male Urogenital Diseases, Pathologic Processes, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Urogenital Diseases, central nervous system malformation, corpus callosum, agenesis of, injury, male reproductive system disorder, nervous system disorder, penile disorder, urinary system disorder | Not yet recruiting | Phase 1 | 2026-03-27 | NCT03463239 | |
| A Trial of Setmelanotide in Patients With Congenital Hypothalamic Obesity (Sub-study of NCT05774756) | Congenital Abnormalities, Congenital Cranial Dysinnervation Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Froelich syndrome, Male Urogenital Diseases, Ocular Motility Disorders, Optic Nerve Hypoplasia, Urogenital Abnormalities, Urogenital Diseases, central nervous system malformation, corpus callosum, agenesis of, cranial nerve neuropathy, disorder of sexual differentiation, endocrine system disorder, eye disorder, gonadal disorder, gonadal dysgenesis, hereditary disease, hypogonadism, nervous system disorder, optic nerve disorder, pituitary stalk interruption syndrome, septooptic dysplasia, third cranial nerve disorder | Recruiting | Phase 3 | 2026-02-12 | NCT06760546 |