ID
44226
Description
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 prior medication form. It has to be filled in for screening.
Mots-clés
Versions (3)
- 15/04/2019 15/04/2019 -
- 15/04/2019 15/04/2019 -
- 20/09/2021 20/09/2021 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
20 septembre 2021
DOI
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Licence
Creative Commons BY-NC 3.0
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Comparison of pharmacokinetic and tolerability of ropinirole in healthy adults, 101468/198
Prior Medication
- StudyEvent: ODM
Description
Prior Medication
Alias
- UMLS CUI-1
- C2826257
Description
If 'YES', please record the medications below.
Type de données
boolean
Alias
- UMLS CUI [1]
- C3166216
- UMLS CUI [2]
- C0013231
Description
(Trade Name Preferred)
Type de données
text
Alias
- UMLS CUI [1]
- C2360065
Description
Single Dose/Unit
Type de données
text
Alias
- UMLS CUI [1]
- C1960417
Description
Frequency of this Dose
Type de données
text
Alias
- UMLS CUI [1]
- C3476109
Description
Route
Type de données
text
Alias
- UMLS CUI [1]
- C0013153
Description
Indication
Type de données
text
Alias
- UMLS CUI [1,1]
- C3146298
- UMLS CUI [1,2]
- C0013227
Description
Duration of therapy
Type de données
text
Alias
- UMLS CUI [1]
- C0444921
Description
Day/Month/Year
Type de données
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Description
Continuing at end of study
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1553904
- UMLS CUI [1,2]
- C2983670
Similar models
Prior Medication
- StudyEvent: ODM
C0013231 (UMLS CUI [2])
C0013227 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C2983670 (UMLS CUI [1,2])
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