ID
44003
Beskrivning
Study ID: 100690 Clinical Study ID: NKP100690 Study Title: A randomised, double blind triple dummy, placebo controlled balanced incomplete block crossover study to evaluate the change in response to a 7% CO2 challenge and pharmacokinetics of single oral doses of GW597599 and paroxetine (5 or 7.5 mg) either alone or in combination, or alprazolam (0.75 mg) 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: paroxetine Trade Name: Tagonis,Seroxat,Paxil,Paroxat,Deroxat,Aropax Study Indication: Depressive Disorder and Anxiety Disorders CRF Seiten: 255-365
Nyckelord
Versioner (2)
- 2017-10-18 2017-10-18 -
- 2021-09-20 2021-09-20 -
Rättsinnehavare
GSK
Uppladdad den
20 september 2021
DOI
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Licens
Creative Commons BY-NC 3.0
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7% CO2, GW597599, paroxetine andor alprazolam in healthy volunteers 100690
Screening; Prior Medication
- StudyEvent: ODM
Beskrivning
Prior Medication
Alias
- UMLS CUI-1
- C2826257
Beskrivning
Prior Medication
Alias
- UMLS CUI-1
- C2826257
Beskrivning
Drug Name
Datatyp
text
Alias
- UMLS CUI [1]
- C0013227
Beskrivning
Drug Dosage
Datatyp
text
Alias
- UMLS CUI [1]
- C0870450
Beskrivning
Frequency
Datatyp
text
Alias
- UMLS CUI [1]
- C3476109
Beskrivning
Administration Route
Datatyp
text
Alias
- UMLS CUI [1]
- C0013153
Beskrivning
Indication
Datatyp
text
Alias
- UMLS CUI [1,1]
- C3146298
- UMLS CUI [1,2]
- C0013227
Beskrivning
Therapy duration
Datatyp
text
Alias
- UMLS CUI [1]
- C0444921
Beskrivning
End Date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Beskrivning
Continuing medication
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2826666
Similar models
Screening; Prior Medication
- StudyEvent: ODM
C0013227 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])