Nephropathic Cystinosis 
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3 Trials

   

Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
Nephropathic Cystinosis
NCT00850317: Fanconi Anemia Transplant Lacking Genotypically Identical Donor

Not yet recruiting
2
25
US
Miltenyi CliniMACs device
Children's Hospital Boston, Dana-Farber Cancer Institute
Fanconi Anemia
04/12
 
NCT01995305: Use Massive Parallel Sequencing and Exome Capture Technology to Sequence the Exome of Fanconi Anemia Children and Their Patents

Available
N/A
RoW
human whole exome, whole genomic, whole exome
Xiaofan Zhu
Fanconi Anemia, Autosomal or Sex Linked Recessive Genetic Disease, Bone Marrow Hematopoiesis Failure, Multiple Congenital Abnormalities, and Susceptibility to Neoplastic Diseases., Hematopoiesis Maintainance.
 
 
CCIR, NCT01327807: Cure Cystinosis International Registry

Recruiting
N/A
750
US
Cystinosis Research Foundation
Cystinosis, Nephropathic Cystinosis, Renal Fanconi Syndrome
12/20
12/22

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