ID
43779
Beschrijving
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
Trefwoorden
Versies (2)
- 24-07-17 24-07-17 -
- 20-09-21 20-09-21 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
20 september 2021
DOI
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Licentie
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
Beschrijving
Prior Medication
Alias
- UMLS CUI-1
- C0013227
Beschrijving
If Yes, please record the medications below.
Datatype
boolean
Alias
- UMLS CUI [1]
- C0013227
Beschrijving
drug name
Datatype
text
Alias
- UMLS CUI [1]
- C0013227
Beschrijving
dosage
Datatype
text
Alias
- UMLS CUI [1]
- C0178602
Beschrijving
frequency of this dose
Datatype
text
Alias
- UMLS CUI [1]
- C3476109
Beschrijving
administration route
Datatype
text
Alias
- UMLS CUI [1]
- C0013153
Beschrijving
medication indication
Datatype
text
Alias
- UMLS CUI [1]
- C3146298
Beschrijving
duration of therapy
Datatype
text
Alias
- UMLS CUI [1]
- C0444921
Beschrijving
medication end date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0806020
- UMLS CUI [1,2]
- C0013227
Beschrijving
continuing medication at end of study
Datatype
boolean
Alias
- UMLS CUI [1]
- C1553904
Beschrijving
Baseline Signs Ans Symptoms
Alias
- UMLS CUI-1
- C0037088
- UMLS CUI-2
- C1442488
Beschrijving
diagnosis
Datatype
text
Alias
- UMLS CUI [1]
- C0011900
Beschrijving
onset date and time
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C2981441
- UMLS CUI [1,2]
- C1442488
Beschrijving
end date and time
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C2981425
- UMLS CUI [1,2]
- C1442488
Beschrijving
outcome
Datatype
text
Alias
- UMLS CUI [1]
- C1705586
Beschrijving
event course
Datatype
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0750729
Beschrijving
intensity
Datatype
text
Alias
- UMLS CUI [1]
- C0518690
Beschrijving
relationship to study procedures
Datatype
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C1510821
Beschrijving
If Yes, please record on Prior Medication form.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0559546
- UMLS CUI [1,2]
- C0087111
Beschrijving
subject withdrawn due to event
Datatype
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])