DDrare
Disease
Drug
Target Gene/Pathway
問合せ先
EN
115. 遺伝性周期性四肢麻痺
Hereditary periodic paralysis
Clinical trials
/
Disease details
臨床試験数
:
1
/
薬物数
:
2
- (
DrugBank
:
2
) /
標的遺伝子数
:
13
-
標的パスウェイ数
:
7
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No.
TrialID
Date_
enrollment
Date_
registration
Public_title
Scientific_title
Condition
Intervention
Primary_
sponsor
Secondary_
sponsor
Recruitment_
Status
Inclusion_
agemin
Inclusion_
agemax
Inclusion_
gender
Target_
size
Phase
Countries
1
NCT00839501
(
ClinicalTrials.gov
)
December 2008
5/2/2009
Effect of Potassium and
Acetazolamide
on People With Andersen-Tawil Syndrome
Therapeutic Trial of Potassium and
Acetazolamide
in Andersen-Tawil Syndrome
Andersen-Tawil Syndrome
Dietary Supplement:
Potassium
;Drug:
Acetazolamide
University of Rochester
Office of Rare Diseases (ORD);Rare Diseases Clinical Research Network;National Institute of Neurological Disorders and Stroke (NINDS)
Office of Rare Diseases (ORD);Rare Diseases Clinical Research Network;National Institute of Neurolog ...
Terminated
10 Years
N/A
Both
3
Phase 1
United States;United Kingdom