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Trial Match

Clinical trials test new treatments — sometimes the newest options available for a disease. Find trials that are recruiting now, near you. Open one to see its eligibility rules as simple questions to go through with your doctor.

Know your stage or your test results (such as EGFR, HER2 or BRCA)? Match trials to your own profile - nothing you type is saved.

🎯 Match trials to me

15 recruiting trials

for Genetic of Intellectual Deficiency

Data Collection Study of Patients With Non-Malignant Disorders Undergoing UCBT, BMT or PBSCT With RIC NCT04528355n/a1 site📍 Pittsburgh Paul Szabolcs · Tests: data collection Triheptanoin for Children With Primary-Specific Pyruvate Dehydrogenase Complex (PDC) Deficiency NCT06340685Phase 11 site📍 Pittsburgh Jirair Krikor Bedoyan · Tests: Triheptanoin Patterns of Neurodevelopmental Disorders NCT06213090n/a1 site📍 Phoenix Richard Frye Natural History of Dysregulation and Aging of the Immune System in People With Trisomy 21 With and Without Thymectomy NCT07416201n/a1 site📍 Bethesda National Institute of Allergy and Infectious Diseases (NIAI… Genetic of Intellectual Deficiency and Autism Spectrum Disorders (RaDiCo-GenIDA) NCT06871696n/a1 site📍 Paris Institut National de la Santé Et de la Recherche Médicale, … UCB Transplant of Inherited Metabolic Diseases With Administration of Intrathecal UCB Derived Oligodendrocyte-Like Cells NCT02254863Phase 11 site📍 Durham Joanne Kurtzberg, MD · Tests: DUOC-01 A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders NCT06092346n/a1 site📍 Bethesda National Human Genome Research Institute (NHGRI) Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford NCT01793168n/a2 sites📍 Sioux Falls📍 Sydney Sanford Health Natural History and Advanced Genetic Study of Pyruvate Dehydrogenase Complex Deficiencies NCT03056794n/a1 site📍 Pittsburgh University of Pittsburgh · Tests: No intervention MPS (RaDiCo Cohort) (RaDiCo-MPS) NCT06036693n/a23 sites📍 Angers📍 Bordeaux📍 Brest Institut National de la Santé Et de la Recherche Médicale, … Institutional Registry of Rare Diseases NCT06573723n/a1 site📍 Buenos Aires Hospital Italiano de Buenos Aires Congenital Muscle Disease Study of Patient and Family Reported Medical Information NCT01403402n/a1 site📍 Lakewood Cure CMD Reduced Intensity Conditioning for Non-Malignant Disorders Undergoing UCBT, BMT or PBSCT NCT01962415Phase 21 site📍 Pittsburgh Paul Szabolcs · Tests: Hydroxyurea, Alemtuzumab, Fludarabine, Melphalan, Thiotepa Efficacy and Safety of the Treatment of Pyruvate Dehydrogenase Deficiency Patients With Glycerol Phenylbutyrate (RAVICTI) NCT06887777Phase 21 site📍 Paris Assistance Publique - Hôpitaux de Paris · Tests: Glycerol Phenylbutyrate 1100 MG/ML [Ravicti] The Myelin Disorders Biorepository Project NCT03047369n/a23 sites📍 Los Angeles📍 Orange📍 Palo Alto Children's Hospital of Philadelphia
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