Non invasive prenatal diagnosis ( DrugBank: - )


3 diseases
告示番号疾患名(ページ内リンク)臨床試験数
8ハンチントン病1
113筋ジストロフィー1
206脆弱X症候群1

8. ハンチントン病


臨床試験数 : 242 薬物数 : 205 - (DrugBank : 62) / 標的遺伝子数 : 85 - 標的パスウェイ数 : 159
No.TrialIDDate_
enrollment
Date_
registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
Secondary_
sponsor
Recruitment_
Status
Inclusion_
agemin
Inclusion_
agemax
Inclusion_
gender
Target_
size
PhaseCountries
1NCT04698551
(ClinicalTrials.gov)
September 1, 20201/9/2020NIPD on cffDNA for Triplet Repeat DiseasesComparison of Two NGS Phasing Techniques of Parental Haplotypes for NIPD of Triplet Expansion DiseasesMyotonic Dystrophy 1;Huntington Disease;Fragile X SyndromeGenetic: Non invasive prenatal diagnosisUniversity Hospital, MontpellierAgence de La BiomédecineActive, not recruiting18 MonthsN/AAll36France

113. 筋ジストロフィー


臨床試験数 : 646 薬物数 : 471 - (DrugBank : 105) / 標的遺伝子数 : 59 - 標的パスウェイ数 : 170
No.TrialIDDate_
enrollment
Date_
registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
Secondary_
sponsor
Recruitment_
Status
Inclusion_
agemin
Inclusion_
agemax
Inclusion_
gender
Target_
size
PhaseCountries
1NCT04698551
(ClinicalTrials.gov)
September 1, 20201/9/2020NIPD on cffDNA for Triplet Repeat DiseasesComparison of Two NGS Phasing Techniques of Parental Haplotypes for NIPD of Triplet Expansion DiseasesMyotonic Dystrophy 1;Huntington Disease;Fragile X SyndromeGenetic: Non invasive prenatal diagnosisUniversity Hospital, MontpellierAgence de La BiomédecineActive, not recruiting18 MonthsN/AAll36France

206. 脆弱X症候群


臨床試験数 : 108 薬物数 : 91 - (DrugBank : 36) / 標的遺伝子数 : 52 - 標的パスウェイ数 : 77
No.TrialIDDate_
enrollment
Date_
registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
Secondary_
sponsor
Recruitment_
Status
Inclusion_
agemin
Inclusion_
agemax
Inclusion_
gender
Target_
size
PhaseCountries
1NCT04698551
(ClinicalTrials.gov)
September 1, 20201/9/2020NIPD on cffDNA for Triplet Repeat DiseasesComparison of Two NGS Phasing Techniques of Parental Haplotypes for NIPD of Triplet Expansion DiseasesMyotonic Dystrophy 1;Huntington Disease;Fragile X SyndromeGenetic: Non invasive prenatal diagnosisUniversity Hospital, MontpellierAgence de La BiomédecineActive, not recruiting18 MonthsN/AAll36France