ID
22108
Description
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
Lien
https://clinicaltrials.gov/ct2/show/NCT00688207?term=NCT00688207&rank=1
Mots-clés
Versions (2)
- 08/05/2017 08/05/2017 -
- 20/05/2017 20/05/2017 -
Téléchargé le
20 mai 2017
DOI
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Licence
Creative Commons BY-NC 3.0
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Follow-Up Urinalysis Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941
Follow-Up Urinalysis Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941
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Follow-Up Urinalysis Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941
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