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Results for “Single-Gene Defects”

9 trials

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Showing 9 of 9 results

Not applicableUnknownNCT05739890
What this trial is testing

Whole Genome Sequencing (WGS) on IVF Embryos and Individual Patients

Who this might be right for
Fertility IssuesSingle-Gene Defects
GenEmbryomics Pty. Ltd 100
Not applicableLooking for participantsNCT01192048
What this trial is testing

Genetics of Congenital Heart Disease

Who this might be right for
Congenital Heart Disease
Nationwide Children's Hospital 5,000
Early research (Phase 1)Study completedNCT06600425
What this trial is testing

Assess the Safety, Tolerability, Ciliary Rescue, and Pharmacodynamics of RCT1100 in Adults With PCD

Who this might be right for
Primary Ciliary Dyskinesia
ReCode Therapeutics 7
Not applicableUnknownNCT00064597
What this trial is testing

Noninvasive Prenatal Diagnosis: Using Fetal Cells From Maternal Blood

Who this might be right for
Chromosome Disorders
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) 3,500
Early research (Phase 1)Study completedNCT05737485
What this trial is testing

Study Evaluating the Safety and Tolerability of RCT1100 in Healthy and PCD Subjects

Who this might be right for
Primary Ciliary Dyskinesia
ReCode Therapeutics 9
Testing effectiveness (Phase 2)UnknownNCT01278277
What this trial is testing

Saffron Supplementation in Stargardt's Disease

Who this might be right for
Retinal DegenerationGenetic DiseaseSingle-Gene Defects+1 more
Catholic University of the Sacred Heart 30
Not applicableUnknownNCT06165055
What this trial is testing

Single Gene Polymorphisms Associated With Molar-Incisor Hypomineralization

Who this might be right for
Molar-Incisor Hypomineralization
Marmara University 120
Testing effectiveness (Phase 2)Active Not RecruitingNCT02610582
What this trial is testing

Safety and Efficacy of rAAV.hCNGA3 Gene Therapy in Patients With CNGA3-linked Achromatopsia

Who this might be right for
Achromatopsia
STZ eyetrial 13
Not applicableUnknownNCT03589079
What this trial is testing

Delineation of Novel Monogenic Disorders in the United Arab Emirates Population

Who this might be right for
Mendelian DisordersGenetic DisorderNovel Mutation+4 more
Imperial College London Diabetes Centre 150