DDrare
Disease
Drug
Target Gene/Pathway
問合せ先
EN
149. 片側痙攣・片麻痺・てんかん症候群
Hemiconvulsion hemiplegia epilepsy syndrome
Clinical trials
/
Disease details
臨床試験数
:
25
/
薬物数
:
35
- (
DrugBank
:
13
) /
標的遺伝子数
:
16
-
標的パスウェイ数
:
22
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TrialID
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Date_
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Scientific_title
Condition
Intervention
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sponsor
Secondary_
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Status
Inclusion_
agemin
Inclusion_
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Inclusion_
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Phase
Countries
1
NCT03857607
(
ClinicalTrials.gov
)
September 1, 2018
26/2/2019
Natural History Study of ATP1A3-related Disease
Natural History of ATP1A3-related Disease: a Deep Phenotyping-genotyping Project
ATP1A3-related Disease;Alternating Hemiplegia of Childhood;Rapid Onset Dystonia Parkinsonism;CAPOS
Genetic:
Whole exome sequencing
Institute of Child Health
Great Ormond Street Hospital for Children NHS Foundation Trust;University College, London
Recruiting
6 Months
60 Years
All
100
United Kingdom