[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"condition:autosomal-dominant-intellectual-disability-craniofacial-dysmorphism-macrocephaly-hypotonia-syndrome-due-to-h1-4-mutation":3},{"name":4,"total":5,"recruiting":5,"trials":6,"biomarkers":21,"states":22},"Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1-4 mutation",2,[7,15],{"nct_id":8,"title":9,"phases":10,"status":12,"updated_at":13,"content_modified":14},"NCT07224581","Beeline: A Phase 3 Study in GRIN-related Neurodevelopmental Disorder",[11],"Phase 3","RECRUITING","2026-08-26T02:19:30.857183Z","2026-05-05T02:43:27.128284Z",{"nct_id":16,"title":17,"phases":18,"status":12,"updated_at":19,"content_modified":20},"NCT06776341","Natural History Study of GEMIN-5 Related Neurodevelopmental Disorder",[],"2026-08-26T02:18:16.220328Z","2026-05-13T02:55:06.576859Z",[],[]]