About: Efficacy Study of DX-88 (Ecallantide) to Treat Acute Attacks of Hereditary Angioedema (HAE)

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About: Efficacy Study of DX-88 (Ecallantide) to Treat Acute Attacks of Hereditary Angioedema (HAE) Goto Sponge NotDistinct Permalink

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clinical trial

Attributes	Values
rdf:type	Item
description	clinical trial (en) ensayu clínicu (ast) klinisch onderzoek (nl) клінічне випробування (uk)
rdfs:label	Efficacy Study of DX-88 (Ecallantide) to Treat Acute Attacks of Hereditary Angioedema (HAE) (en) Efficacy Study of DX-88 (nl)
skos:prefLabel	Efficacy Study of DX-88 (Ecallantide) to Treat Acute Attacks of Hereditary Angioedema (HAE) (en) Efficacy Study of DX-88 (nl)
name	Efficacy Study of DX-88 (Ecallantide) to Treat Acute Attacks of Hereditary Angioedema (HAE) (en) Efficacy Study of DX-88 (nl)
title	wds:Q65384975-E1B8E506-B452-4869-B7F4-6B1F8055E271
title	EDEMA4: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Assess the Efficacy and Safety of DX-88 (Ecallantide) for the Treatment of Acute Attacks of Hereditary Angioedema (en)
end time	wds:Q65384975-F1803E47-122C-42D4-AE71-396D004EACF7
end time	2008-06-01 00:00:00Z (xsd:dateTime)
instance of	wds:Q65384975-818613FD-52EB-4902-B394-57D5E6F32053
instance of	clinical trial
start time	wds:Q65384975-5B15671A-F939-41F9-B893-5F4B30F92C0A
start time	2007-04-01 00:00:00Z (xsd:dateTime)
country	wds:Q65384975-4E104788-DA06-4F54-807F-3A8007EC9861 wds:Q65384975-7BDD9C94-6AFB-42B9-B1CD-8A3AFD2EEDEC wds:Q65384975-94A97A6F-8191-41D8-A560-800E71CD973F
country	Malawi United States of America Jordan
research site	wds:Q65384975-07E2C846-21D6-4CF5-9561-161217057F92 wds:Q65384975-16F546EF-0234-4D7D-BB94-71CB2D49CE92 wds:Q65384975-40973B06-809D-42F0-8313-00E98150B6E2 wds:Q65384975-52EBB2ED-3038-43F2-959D-CF4F6EFD536F wds:Q65384975-627B643C-196B-45E2-913A-4ACE34D4A980 wds:Q65384975-867F5D8E-A97F-49B5-9BEC-625DAACD9A10 wds:Q65384975-A7DFB065-6CBB-4D34-8335-6D6EFA706EAC wds:Q65384975-BB38B96D-C952-4F7B-92BD-7BE8763FB78E wds:Q65384975-CB0B208C-26EA-46C4-A9DB-A57378FF0397 wds:Q65384975-CBF910D4-9AE4-481B-A636-8C4C30A1BC33 wds:Q65384975-DEA2469D-5AFB-4C41-8B18-2634AFC847B7 wds:Q65384975-E840F4CF-2262-4214-88F2-F899DE851C88
research site	University of Toronto Christiana Hospital Pennsylvania State University Georgetown University Arkansas Children's Hospital Jordan University of Science and Technology Brigham and Women's Hospital University of Cincinnati University of Nevada, Reno School of Medicine University of South Florida Clinical Research Associates of Tidewater University of Utah Health Care
minimum age	wds:Q65384975-FA4CF771-DD10-4BED-812D-8DE150527153
minimum age	10 (xsd:decimal)
medical condition	wds:Q65384975-C4E46940-0638-4D25-B06E-0F7C1E83CAB1
medical condition	angioedema
number of participants	wds:Q65384975-26D2AD64-ED33-41E4-AFB9-53396FEFAF30
number of participants	96 (xsd:decimal)
study type	wds:Q65384975-E46FBC95-D064-4200-87E7-984D7A46448F
study type	interventional study
ClinicalTrials.gov ID	wds:Q65384975-78D0EC79-2D27-40C0-B374-54967B3FCB3A
ClinicalTrials.gov ID	NCT00457015
clinical trial phase	wds:Q65384975-458FCB78-A683-4A83-96A2-0058EA60D897
clinical trial phase	phase III clinical trial
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q65384975

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