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Teacsa sgrùdaidh oifigeil (Beurla)

Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network

A’ fastadhSgrùdadh amharcFàilte do shaor-thoilich fhallain
1 Month – 100 Years · Gach gnè · Air ùrachadh 2 Dàmh 2026 · NCT02450851

Genetic Study to Determine the Cause of Birth Defects in Newborns in Texas

A’ fastadhFàilte do shaor-thoilich fhallain
1 Day – 90 Days · Gach gnè · Air ùrachadh 1 Dàmh 2026 · NCT07102966

Odevixibat Pregnancy and Lactation Surveillance Program: A Study to Evaluate the Safety of Odevixibat During Pregnancy and/or Lactation

A’ fastadhSgrùdadh amharc
Gach aois · Banairean · Air ùrachadh 1 Dàmh 2026 · NCT06258902

A Study of SGT-212 Gene Therapy in Friedreich's Ataxia

A’ fastadhÌre 1
Aoisean 18 gu 40 · Gach gnè · Air ùrachadh 29 Sult 2026 · NCT07180355

RAPA-501 Therapy for ALS

A’ fastadhÌre 2/3
Aoisean 18 agus nas sine · Gach gnè · Air ùrachadh 29 Sult 2026 · NCT04220190

Diagnosis and Treatment of Patients With Inborn Errors of Metabolism

A’ fastadhSgrùdadh amharcFàilte do shaor-thoilich fhallain
1 Month – 115 Years · Gach gnè · Air ùrachadh 22 Sult 2026 · NCT00369421

Human Biospecimen Procurement Protocol: Biorepository to Support Translational Research to Identify Disease Mechanism(s)

A’ fastadhSgrùdadh amharcFàilte do shaor-thoilich fhallain
1 Month – 100 Years · Gach gnè · Air ùrachadh 22 Sult 2026 · NCT02543996

A First-in-human Study of KK8123 in Adults With X-linked Hypophosphatemia

A’ fastadhÌre 1/2
Aoisean 18 gu 65 · Gach gnè · Air ùrachadh 21 Sult 2026 · NCT06525636

Caregiving Networks Across Disease Context and the Life Course

A’ fastadhSgrùdadh amharcFàilte do shaor-thoilich fhallain
Aoisean 18 gu 100 · Gach gnè · Air ùrachadh 15 Sult 2026 · NCT05007990

Longitudinal Studies of Patient With FPDMM

A’ fastadhSgrùdadh amharcFàilte do shaor-thoilich fhallain
1 Day – 100 Years · Gach gnè · Air ùrachadh 11 Sult 2026 · NCT03854318

Friedreich Ataxia Global Clinical Consortium UNIFIED Natural History Study

A’ fastadhSgrùdadh amharcFàilte do shaor-thoilich fhallain
Gach aois · Gach gnè · Air ùrachadh 1 Sult 2026 · NCT06016946

Elafibranor Pregnancy Surveillance Program: A Study to Evaluate the Safety of Elafibranor During Pregnancy

A’ fastadhSgrùdadh amharc
Gach aois · Banairean · Air ùrachadh 31 Lùna 2026 · NCT07556913

International Rare Brain Tumor Registry

A’ fastadhSgrùdadh amharc
Suas gu aois 45 · Gach gnè · Air ùrachadh 7 Lùna 2026 · NCT05697874

Stakeholders of Rare Diseases Informing Values In Neuroethics

A’ fastadhSgrùdadh amharc
Gach aois · Gach gnè · Air ùrachadh 13 Iuch 2026 · NCT07314736

Evaluation of an Advanced Lower Extremity Neuroprostheses

A’ fastadh
Aoisean 21 gu 75 · Gach gnè · Air ùrachadh 10 Iuch 2026 · NCT00623389

A Study Evaluating the Real-World Experience of Givinostat in Patients With Duchenne Muscular Dystrophy

A’ fastadhSgrùdadh amharc
Aoisean 6 agus nas sine · Gach gnè · Air ùrachadh 2 Iuch 2026 · NCT07127978

Study of S-606001 as an Add-on to Enzyme Replacement Therapy (ERT) in Participants With Late-onset Pompe Disease (LOPD)

A’ fastadhÌre 2
Aoisean 18 agus nas sine · Gach gnè · Air ùrachadh 23 Ògmh 2026 · NCT07123155

Baker Gordon Syndrome Natural History Study

A’ fastadhSgrùdadh amharc
Aoisean 0 gu 99 · Gach gnè · Air ùrachadh 3 Ògmh 2026 · NCT06399952

UW Undiagnosed Genetic Diseases Program

A’ fastadhSgrùdadh amharc
Suas gu aois 100 · Gach gnè · Air ùrachadh 29 Cèit 2026 · NCT04586075

Direct to Patient Minimal Risk Biospecimen and Data Collection Research

A’ fastadhSgrùdadh amharcFàilte do shaor-thoilich fhallain
Aoisean 18 gu 90 · Gach gnè · Air ùrachadh 5 Cèit 2026 · NCT07128966

A Randomized Study of SPK-10001 Gene Therapy in Participants With Huntington's Disease

A’ fastadhÌre 1/2
Aoisean 25 gu 65 · Gach gnè · Air ùrachadh 5 Cèit 2026 · NCT06826612

A Study of AAV9 Gene Therapy in Participants With Canavan Disease (CANaspire Clinical Trial)

A’ fastadhÌre 1/2
30 Months · Gach gnè · Air ùrachadh 17 Gibl 2026 · NCT04998396

Gene Discovery Core, The Manton Center

A’ fastadhSgrùdadh amharc
Gach aois · Gach gnè · Air ùrachadh 25 Màrt 2026 · NCT02743845

Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome

A’ fastadhSgrùdadh amharc
Gach aois · Gach gnè · Air ùrachadh 17 Gearr 2026 · NCT05528744

MIHRA - Patient-Rooted Insights for Shaping Myositis Science (PRISMS)

A’ fastadhSgrùdadh amharc
Aoisean 7 agus nas sine · Gach gnè · Air ùrachadh 28 Faoi 2026 · NCT07374107

Bho ClinicalTrials.gov, dàta air a thogail 6 Dàmh 2026. Bidh gach sgrùdadh a’ suidheachadh a chuidi fhèin; bidh an sgioba sgrùdaidh a’ co-dhùnadh cò as urrainn pàirt a ghabhail.