ID
22159
Beschrijving
The present pharmacokinetic study is designed to assess the pharmacokinetics of RSG XR as monotherapy in patients with mild Alzheimer's disease (AD) as such information will not be obtained from the current phase III trials . The study aims to enroll fourteen patients (seven of each APOE genotype). Each patient will receive a single oral dose of 4mg of RSG XR in the morning under fasted conditions and PK samples will be taken up to 36h. GSK Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00688207?term=NCT00688207&rank=1
Link
https://clinicaltrials.gov/ct2/show/NCT00688207?term=NCT00688207&rank=1
Trefwoorden
Versies (2)
- 09-05-17 09-05-17 -
- 22-05-17 22-05-17 -
Geüploaded op
22 mei 2017
DOI
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Licentie
Creative Commons BY-NC 3.0
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Pharmacokinetics Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941
Pharmacokinetics Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941
Beschrijving
Meal
Alias
- UMLS CUI-1
- C0016452
Beschrijving
Start Date
Datatype
date
Maateenheden
- Day Month Year
Alias
- UMLS CUI [1,1]
- C0016452
- UMLS CUI [1,2]
- C0808070
Beschrijving
Planned Relative Time
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0016452
- UMLS CUI [1,2]
- C0439564
Beschrijving
Start time
Datatype
time
Maateenheden
- hr:min
Alias
- UMLS CUI [1,1]
- C0016452
- UMLS CUI [1,2]
- C1301880
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Pharmacokinetics Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941
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C0439564 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0439564 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])
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