ID
39187
Descripción
Study ID: 103106 Clinical Study ID: WXL103106 Study Title:An open-label, 2-period, sequential treatment, 1-way drug interaction study to evaluate the effect of ritonavir on bupropion pharmacokinetics in healthy volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: bupropion Trade Name: Wellbutrin,QUOMEM,Elontril,Zyban,ZYNTABAC; Zyban,ZYNTABAC,Wellbutrin,Wellburin,QUOMEM,Prolev,Magerion,Geronplase,Elontril Study Indication: Depressive Disorder
Palabras clave
Versiones (1)
- 8/12/19 8/12/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
8 de diciembre de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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Effect of Ritonavir on Bupropion Pharmacokinetics; 103106
PGx - Pharmacogenetic Research
- StudyEvent: ODM
Descripción
Consent for PGx-Pharmacogenetic Research
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0021430
Descripción
Pharmacogenetic Test, Informed Consent
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
Descripción
Pharmacogenetic Test, Informed Consent, Date in time
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0011008
Descripción
Pharmacogenetic Test, Informed Consent, Reason and justification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0566251
Descripción
Pharmacogenetic Test, Informed Consent, Reason and justification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0566251
Descripción
Blood Sample Collection (DNA)
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0005834
Descripción
Pharmacogenetic Test, Collection of blood specimen for laboratory procedure
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0005834
Descripción
Pharmacogenetic Test, Collection of blood specimen for laboratory procedure, Date in time
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0005834
- UMLS CUI [1,3]
- C0011008
Descripción
Withdrawal of Consent
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0021430
- UMLS CUI-3
- C2349954
Descripción
Blood Sample Destruction
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0178913
- UMLS CUI-3
- C1948029
Descripción
Pharmacogenetic Test, Blood specimen, Destruction, Request
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
Descripción
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0566251
Descripción
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0566251
Similar models
PGx - Pharmacogenetic Research
- StudyEvent: ODM
C0021430 (UMLS CUI-2)
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C0005834 (UMLS CUI-2)
C0005834 (UMLS CUI [1,2])
C0005834 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0021430 (UMLS CUI-2)
C2349954 (UMLS CUI-3)
C0021430 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0178913 (UMLS CUI-2)
C1948029 (UMLS CUI-3)
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,5])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,5])