ID
32027
Description
Study ID: 105548 Clinical Study ID: HZA105548 Study Title: A double-blind, randomized, placebo-controlled, repeat dose, 2-way crossover drug interaction study to investigate the pharmacokinetic and pharmacodynamic effects following administration of fluticasone furoate/GW642444M Inhalation Powder with ketoconazole Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01165125 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: fluticasone furoate/vilanterol; vilanterol Trade Name: Relvar; vilanterol Study Indication: Asthma
Mots-clés
Versions (1)
- 14/10/2018 14/10/2018 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
14 octobre 2018
DOI
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Licence
Creative Commons BY-NC 3.0
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Pharmacokinetic and pharmacodynamic effects following administration of fluticasone Inhalation Powder with ketoconazole NCT01165125
Eligibility Question, Subject Identification, Electronically Transferred Lab Data Screening and Day 1 and Randomisation Number
Description
Inclusion Criteria
Alias
- UMLS CUI-1
- C1512693
Description
Inclusion
Type de données
integer
Alias
- UMLS CUI [1]
- C1512693
Description
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
Description
Exclusion Criteria
Type de données
integer
Alias
- UMLS CUI [1]
- C0680251
Description
Subject Identification
Alias
- UMLS CUI-1
- C2348585
Description
Electronically transferred lab data - Screening
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C1320722
Description
Hematology Date and time sample taken
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0018943
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Clinical Chemistry Date and time sample taken
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Urinalysis Date and time sample taken
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Electronically transferred lab data - Day 1
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C1320722
Description
Hematology Date and time sample taken
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0018943
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Clinical Chemistry Date and time sample taken
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Randomisation number
Alias
- UMLS CUI-1
- C1300638
- UMLS CUI-2
- C0034656
Description
Randomisation; Ability
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0085732
Description
Randomisation Number
Type de données
text
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0085732
- UMLS CUI [2,1]
- C1300638
- UMLS CUI [2,2]
- C0034656
Description
Date of randomisation
Type de données
date
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0011008
Similar models
Eligibility Question, Subject Identification, Electronically Transferred Lab Data Screening and Day 1 and Randomisation Number
C1709750 (UMLS CUI [2,1])
C0680251 (UMLS CUI [2,2])
C1709750 (UMLS CUI [3,1])
C1512693 (UMLS CUI [3,2])
C1516637 (UMLS CUI [3,3])
C1320722 (UMLS CUI-2)
C0200345 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0200345 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0200345 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C1320722 (UMLS CUI-2)
C0200345 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0200345 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0085732 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,2])
C1300638 (UMLS CUI [2,1])
C0034656 (UMLS CUI [2,2])
C0011008 (UMLS CUI [1,2])