About: Relative Bioavailability of Two Different Batches of a Linagliptin / Metformin Combination Tablet in Healthy Volunteers

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About: Relative Bioavailability of Two Different Batches of a Linagliptin / Metformin Combination Tablet in Healthy Volunteers Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

clinical trial

Attributes	Values
rdf:type	Item
description	assaig clínic (ca) clinical trial (en) clinical trial (en-ca) clinical trial (en-gb) clinical trial (en-us) ensaio clínico (gl) ensayo clínico (es) ensayu clínicu (ast) essai clinique (fr) klinisch onderzoek (nl) клінічне випробування (uk)
rdfs:label	Relative Bioavailability of Two Different Batches of a Linagliptin / Metformin Combination Tablet in Healthy Volunteers (en)
skos:prefLabel	Relative Bioavailability of Two Different Batches of a Linagliptin / Metformin Combination Tablet in Healthy Volunteers (en)
name	Relative Bioavailability of Two Different Batches of a Linagliptin / Metformin Combination Tablet in Healthy Volunteers (en)
title	wds:Q63818461-F1E0758E-5EBC-433F-9134-C5BE108569EC
title	Relative Bioavailability of Two Different Batches of a 2.5 mg Linagliptin / 1000 mg Metformin Fixed Dose Combination Tablet (FDC) in Healthy Male and Female Volunteers (an Open-label, Randomised, Single Dose, Two-way Crossover, Phase I Trial) (en)
end time	wds:Q63818461-7974E036-5DBE-4732-82C3-747E31E7136B
end time	2010-12-01 00:00:00Z (xsd:dateTime)
instance of	wds:Q63818461-17105781-9ABD-450B-808F-2A1F58955594
instance of	clinical trial
start time	wds:Q63818461-81064D04-A73F-4F28-90E1-F2AA0F72753A
start time	2010-09-01 00:00:00Z (xsd:dateTime)
country	wds:Q63818461-4083C29F-29F0-49B4-B68F-43690A6445C2
country	Germany
research intervention	wds:Q63818461-623501F2-FBD2-470F-8EAC-B445A7C3A574 wds:Q63818461-664B7110-4F03-45A2-9D3E-309C16B52025
research intervention	metformin wd:Q909745
minimum age	wds:Q63818461-C662C821-127A-4706-A7E9-BAA32D422E1D
minimum age	21 (xsd:decimal)
number of participants	wds:Q63818461-124D8E14-7BAC-4EB2-BF01-4AFC50C0D189
number of participants	40 (xsd:decimal)
maximum age	wds:Q63818461-1D404B81-C9C4-4982-BF5C-4FFF81C1AF77
maximum age	50 (xsd:decimal)
study type	wds:Q63818461-6F40CC16-2466-4603-92B6-69AC94166313
study type	interventional study
ClinicalTrials.gov ID	wds:Q63818461-85E401C8-3FE0-412D-97AA-1DD483899D5D
ClinicalTrials.gov ID	NCT01216397
clinical trial phase	wds:Q63818461-0DCFF50B-7F8E-4232-97F1-6A72D33E58D9
clinical trial phase	phase I clinical trial
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q63818461

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