ID
39187
Description
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
Mots-clés
Versions (1)
- 08/12/2019 08/12/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
8 décembre 2019
DOI
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Licence
Creative Commons BY-NC 3.0
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Effect of Ritonavir on Bupropion Pharmacokinetics; 103106
PGx - Pharmacogenetic Research
- StudyEvent: ODM
Description
Consent for PGx-Pharmacogenetic Research
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0021430
Description
Pharmacogenetic Test, Informed Consent
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
Description
Pharmacogenetic Test, Informed Consent, Date in time
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0011008
Description
Pharmacogenetic Test, Informed Consent, Reason and justification
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0566251
Description
Pharmacogenetic Test, Informed Consent, Reason and justification
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0566251
Description
Blood Sample Collection (DNA)
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0005834
Description
Pharmacogenetic Test, Collection of blood specimen for laboratory procedure
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0005834
Description
Pharmacogenetic Test, Collection of blood specimen for laboratory procedure, Date in time
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0005834
- UMLS CUI [1,3]
- C0011008
Description
Withdrawal of Consent
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0021430
- UMLS CUI-3
- C2349954
Description
Blood Sample Destruction
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0178913
- UMLS CUI-3
- C1948029
Description
Pharmacogenetic Test, Blood specimen, Destruction, Request
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
Description
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Type de données
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
Description
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Type de données
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])