drugset / Trial / NCT00479219

Study Evaluating GSI-953 in Healthy Young and Alzheimer's Patients

NCT00479219

Phase 1 Completed 17 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedSingle-groupDouble-blindTreatment

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).

Timeline

Start
2007-05
Primary completion
2007-10
Completion
2007-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Begacestat Small molecule Oral

Indications