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 170. オクシピタル・ホーン症候群 [臨床試験数:1,薬物数:3(DrugBank:3),標的遺伝子数:0,標的パスウェイ数:0] 

Searched query = "Occipital horn syndrome"
The queries were searched in Public_title, Scientific_title, and Condition of the data. Export date: 11/20/2019. Trials are sorted by Date_enrolment from most recent to oldest in the table.

Search in Page    e.g. "Phase 3", "Not recruiting", "Japan"    Synonyms (DrugBank) were also searched for.
No.TrialIDDate_
enrollement
Last_Refreshed_
on
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
Secondary_
sponsor
Recruitment_
Status
Inclusion_
agemin
Inclusion_
agemax
Inclusion_
gender
Target_
size
PhaseCountries
1NCT00811785February 27, 200926 August 2019Molecular Bases of Response to Copper Treatment in Menkes Disease, Related Phenotypes, and Unexplained Copper DeficiencyMolecular Bases of Response to Copper Treatment in Menkes Disease, Related Phenotypes, and Unexplained Copper DeficiencyMenkes Disease;Occipital Horn Syndrome;Unexplained Copper DeficiencyDrug: Copper HistidineEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)National Center for Complementary and Integrative Health (NCCIH)Not recruitingN/A80 YearsAll93Phase 3United States