Abnormalities, Multiple  >>  Phase N/A
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3 Trials

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Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
Abnormalities, Multiple
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.
 
 
ECP-002e, NCT01992289 / 2013-004565-14: Extension Study of XLHED-Affected Male Subjects Treated With EDI200 in Protocol ECP-002

Active, not recruiting
N/A
10
US, Europe
EDI200, APO200
Edimer Pharmaceuticals
X-linked Hypohidrotic Ectodermal Dysplasia
03/25
03/25
NCT03154697: Development of Clinical Database of Individuals With Smith-Magenis Syndrome and Sleep Disturbances

Recruiting
N/A
1000
US
Data collection of sleep disturbances in individuals with SMS
Vanda Pharmaceuticals
Sleep Disturbances in Smith-Magenis Syndrome
12/30
12/30

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