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NCT00479219 · ClinicalTrials.gov registry record · Phase 1
Study Evaluating GSI-953 in Healthy Young and Alzheimer's Patients
A Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
- 17
- Enrollment target
NCT00479219 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 17 participants.
The verdict
NCT00479219, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 17 participants
- Enrollment target
Study Summary
To assess the pharmacodynamics (PD) of biomarkers amyloid beta peptide 40 and 42 (Ab40 and Ab42) in CSF, following single oral doses of GSI-953, an investigational drug, in healthy young subjects and patients with Alzheimer Disease (AD).
Interventions
- OTHER Placebo
- DRUG GSI-953
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 17 participants |
| Start Date | 2007-05 |
| Est. Completion | 2007-10 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00479219
The ClinicalTrials.gov registry entry for NCT00479219 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 17 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00479219 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00479219 about?
NCT00479219 is a clinical study titled "Study Evaluating GSI-953 in Healthy Young and Alzheimer's Patients". To assess the pharmacodynamics (PD) of biomarkers amyloid beta peptide 40 and 42 (Ab40 and Ab42) in CSF, following single oral doses of GSI-953, an investigational drug, in healthy young subjects and patients with Alzheimer Disease (AD).
What is the current status of trial NCT00479219?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 17 participants. The study started on 2007-05. Estimated completion is 2007-10.
What interventions are being tested in trial NCT00479219?
The interventions under investigation include: Placebo (OTHER), GSI-953 (DRUG).
Who is sponsoring clinical trial NCT00479219?
This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.
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