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Sponsored by: |
Wyeth |
Information provided by: | Wyeth |
ClinicalTrials.gov Identifier: | NCT00739037 |
The primary purpose of this study is to assess biomarker known as amyloid beta peptide 40 (Ab40) in Cerebrospinal Fluid (CSF), following a single oral dose of PAZ-417 in subjects with Alzheimer Disease (AD). This study will also consider another biomarker amyloid beta peptide 42 (Ab42) in Cerebrospinal Fluid in subjects with Alzheimer Disease and assess the safety, tolerability and pharmacokinetic profile of PAZ-417 in both plasma and Cerebrospinal Fluid in these subjects.
Condition | Intervention | Phase |
Alzheimer Disease |
Drug: Placebo Drug: PAZ-417 |
Phase I |
Genetics Home Reference related topics: | Alzheimer disease |
MedlinePlus related topics: | Alzheimer's Disease |
Study Type: | Interventional |
Study Design: | Other, Randomized, Double Blind (Subject, Caregiver, Investigator), Single Group Assignment, Pharmacokinetics/Dynamics Study |
Official Title: | A Randomized, Single Dose, Placebo-Controlled, 2 Period Crossover Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of PAZ 417 in Cerebrospinal Fluid, When Administered Orally to Subjects With Alzheimer's Disease |
Estimated Enrollment: | 10 |
Study Start Date: | August 2008 |
Estimated Study Completion Date: | December 2008 |
Estimated Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
A: Placebo Comparator | Drug: Placebo |
B: Experimental | Drug: PAZ-417 |
Ages Eligible for Study: | 55 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion:
Exclusion:
Contact: Trial Manager | clintrialparticipation@wyeth.com |
United States, California | |||||
California Clinical Trials | Recruiting | ||||
Glendale, California, United States, 91026 | |||||
Contact: Trial Manager clinicaltrialparticipation@wyeth.com |
Wyeth |
Study Director: | Medical Monitor | Wyeth |
Responsible Party: | Wyeth ( Wyeth (Registry Contact: Clinical Trial Registry Specialist) ) |
Study ID Numbers: | 3186A1-1103 |
First Received: | August 15, 2008 |
Last Updated: | August 19, 2008 |
ClinicalTrials.gov Identifier: | NCT00739037 |
Health Authority: | United States: Food and Drug Administration |
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