{"disease":{"id":"myt1l-syndrome","name":"myt1l syndrome"},"drugs":{"marketed":[],"pipeline":[],"offLabel":[],"totalMarketed":0,"totalPipeline":0},"trials":{"data":[{"nct_id":"NCT07008612","title":"MYT1L Syndrome: a Rare Paediatric Genetic Syndrome Responsible for a Neurodevelopmental Disorder","phase":"","overall_status":"RECRUITING","enrollment_count":50,"lead_sponsor_name":"University Hospital, Rouen","has_results":false}],"total":1},"guidelines":[],"source":"Drug Landscape verified database"}