ID
36010
Beskrivning
Study ID: 101468/198 Clinical Study ID: 101468/198 Study Title:An open, randomised, crossover, healthy volunteer study to compare the PK and tolerability of ropinirole as 3 different new formulations with the standard marketed formulation and to study the effects of a high fat meal on a new formulation 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: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication : Restless Legs Syndrome The Study consists of a Screening, 5 Sessions each with 2 days and a Follow-up. This document contains the Plasma Drug Assay fomr. It has to be filled in for all Sessions each for both Day 1 and Day 2.
Nyckelord
Versioner (1)
- 2019-04-09 2019-04-09 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
9 april 2019
DOI
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Licens
Creative Commons BY-NC 3.0
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Comparison of pharmacokinetic and tolerability of ropinirole in healthy adults, 101468/198
Plasma Drug Assay
- StudyEvent: ODM
Beskrivning
Plasma Drug Assay
Alias
- UMLS CUI-1
- C1609077
- UMLS CUI-2
- C1261153
Beskrivning
day month year
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0011008
Beskrivning
00:00-23:59
Datatyp
time
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0040223
Beskrivning
Only tick for Day 1.
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0439564
- UMLS CUI [1,2]
- C0178602
Beskrivning
Only tick for Day 2.
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0439564
- UMLS CUI [1,2]
- C0178602
Beskrivning
day month year
Datatyp
date
Alias
- UMLS CUI [1]
- C1302413
Beskrivning
00:00-23:59
Datatyp
time
Alias
- UMLS CUI [1]
- C0040223
Beskrivning
Blood samples taken
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1277698
- UMLS CUI [1,2]
- C1609077
Beskrivning
Initials
Datatyp
text
Alias
- UMLS CUI [1]
- C2986440
Beskrivning
Comments
Datatyp
text
Alias
- UMLS CUI [1]
- C0947611
Similar models
Plasma Drug Assay
- StudyEvent: ODM
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C1609077 (UMLS CUI [1,2])
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