DDrare
Disease
Drug
Target Gene/Pathway
問合せ先
EN
Blood and/or skin biopsy ( DrugBank: - )
2 diseases
告示番号
疾患名
(ページ内リンク)
臨床試験数
90
網膜色素変性症
1
301
黄斑ジストロフィー
1
90. 網膜色素変性症
臨床試験数
:
147
/
薬物数
:
176
- (
DrugBank
:
43
) /
標的遺伝子数
:
49
-
標的パスウェイ数
:
110
10
50
100
ALL
diseases per page:
Showing 1 to 1 of 1 diseases
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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
NCT04658251
(
ClinicalTrials.gov
)
March 3, 2021
1/12/2020
Study of New Mutations in Cone Disorders
Functional Study of Intronic Variants in Inherited Cone Disorders
Retinal Dystrophy, Cone-Rod;Cone Dystrophy;Cone Rod Dystrophy;Macular Degeneration
Genetic:
Blood and/or skin biopsy
University Hospital, Lille
NULL
Recruiting
3 Years
N/A
All
20
France
301. 黄斑ジストロフィー
臨床試験数
:
46
/
薬物数
:
42
- (
DrugBank
:
11
) /
標的遺伝子数
:
9
-
標的パスウェイ数
:
67
10
50
100
ALL
diseases per page:
Showing 1 to 1 of 1 diseases
Filter by
Reset
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
NCT04658251
(
ClinicalTrials.gov
)
March 3, 2021
1/12/2020
Study of New Mutations in Cone Disorders
Functional Study of Intronic Variants in Inherited Cone Disorders
Retinal Dystrophy, Cone-Rod;Cone Dystrophy;Cone Rod Dystrophy;Macular Degeneration
Genetic:
Blood and/or skin biopsy
University Hospital, Lille
NULL
Recruiting
3 Years
N/A
All
20
France