ID
41684
Beschreibung
Study ID: 110106 Clinical Study ID: 110106 Study Title: A single centre, randomized, double-blind, dose ascending, placebo-controlled study, in two parts, to evaluate the safety, tolerability and pharmacokinetics of escalating single and repeat inhaled doses of GSK573719 and placebo formulated with the excipient magnesium stearate, in healthy subjects and in a healthy population of Cytochrome P450 Isoenzyme 2D6 poor metabolisers. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00803673 Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GSK573719, Placebo Study Indication: Pulmonary Disease, Chronic Obstructive
Stichworte
Versionen (1)
- 2020-12-15 2020-12-15 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
15 december 2020
DOI
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Lizenz
Creative Commons BY 4.0
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Safety, tolerability and pharmacokinetics of GSK573719 and placebo formulated with the excipient magnesium stearate NCT00803673
Pharmacogenetic Research
- StudyEvent: ODM
Beschreibung
Pharmacogenetic Research Content
Alias
- UMLS CUI-1
- C0021430
- UMLS CUI-2
- C2347500
Beschreibung
Has informed consent been obtained for PGx-Pharmacogenetic research
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
Beschreibung
Record date informed consent obtained for PGx Pharmacogenetic research
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0011008
Beschreibung
Has a blood sample been collected for PGx-pharmacogenetic (DNA) research?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0005834
Beschreibung
Date sample taken
Datentyp
date
Alias
- UMLS CUI [1]
- C1302413
Beschreibung
If informed consent has not been obtained, check reason
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
- UMLS CUI [1,3]
- C0566251
Beschreibung
Specify other reason for consent has not been obtained
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
- UMLS CUI [2,1]
- C0566251
- UMLS CUI [2,2]
- C0205394
- UMLS CUI [2,3]
- C2348235
Beschreibung
Pharmacogenetic Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C1707492
- UMLS CUI-2
- C0031325
Beschreibung
Has subject withdrawn consent for PGx research?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0031325
Beschreibung
Has a request been made for sample destruction?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
Beschreibung
Record reason for request been made for sample destruction
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
- UMLS CUI [1,4]
- C0392360
Beschreibung
Specify other reason for request been made for sample destruction
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
- UMLS CUI [2,1]
- C0392360
- UMLS CUI [2,2]
- C0205394
Ähnliche Modelle
Pharmacogenetic Research
- StudyEvent: ODM
C2347500 (UMLS CUI-2)
C2347500 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,2])
C2347500 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C2347500 (UMLS CUI [1,2])
C0566251 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C2348235 (UMLS CUI [2,3])
C0031325 (UMLS CUI-2)
C0031325 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,2])
C1272683 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,2])
C1272683 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1272683 (UMLS CUI [1,3])
C0392360 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
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