ID
24050
Description
Study ID: 100716 Clinical Study ID: NKP100716 Study Title: An open label repeat dose study to investigate the effect of GW597599 (15 mg) and paroxetine (10 mg) given in combination for 15 days on the pharmacokinetics of midazolam and dextromethorphan in healthy male and female 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: vestipitant Trade Name: paroxetine and vestipitant Study Indication: Depressive Disorder and Anxiety Disorders Documentation part: Pharmacogenetic Research, Prior And Concomitant Medication, Baseline Signs and Symptoms
Mots-clés
Versions (2)
- 24/07/2017 24/07/2017 -
- 20/09/2021 20/09/2021 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
24 juillet 2017
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Pharmacogenetic Research, Prior And Concomitant Medication, Baseline Signs And Symptoms
GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Pharmacogenetic Research, Prior And Concomitant Medication, Baseline Signs And Symptoms
Description
Prior Medication
Alias
- UMLS CUI-1
- C0013227
Description
If Yes, please record the medications below.
Type de données
boolean
Alias
- UMLS CUI [1]
- C0013227
Description
drug name
Type de données
text
Alias
- UMLS CUI [1]
- C0013227
Description
dosage
Type de données
text
Alias
- UMLS CUI [1]
- C0178602
Description
frequency of this dose
Type de données
text
Alias
- UMLS CUI [1]
- C3476109
Description
administration route
Type de données
text
Alias
- UMLS CUI [1]
- C0013153
Description
medication indication
Type de données
text
Alias
- UMLS CUI [1]
- C3146298
Description
duration of therapy
Type de données
text
Alias
- UMLS CUI [1]
- C0444917
Description
medication end date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0806020
- UMLS CUI [1,2]
- C0013227
Description
continuing medication at end of study
Type de données
boolean
Alias
- UMLS CUI [1]
- C1553904
Description
Baseline Signs Ans Symptoms
Alias
- UMLS CUI-1
- C0037088
- UMLS CUI-2
- C1442488
Description
diagnosis
Type de données
text
Alias
- UMLS CUI [1]
- C0011900
Description
onset date and time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C2981441
- UMLS CUI [1,2]
- C1442488
Description
end date and time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C2981425
- UMLS CUI [1,2]
- C1442488
Description
outcome
Type de données
text
Alias
- UMLS CUI [1]
- C1705586
Description
event course
Type de données
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0750729
Description
intensity
Type de données
text
Alias
- UMLS CUI [1]
- C0518690
Description
relationship to study procedures
Type de données
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C1510821
Description
If Yes, please record on Prior Medication form.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0559546
- UMLS CUI [1,2]
- C0087111
Description
subject withdrawn due to event
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0877248
Similar models
GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Pharmacogenetic Research, Prior And Concomitant Medication, Baseline Signs And Symptoms
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C1442488 (UMLS CUI-2)
C1442488 (UMLS CUI [1,2])
C1442488 (UMLS CUI [1,2])
C1510821 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,2])