Safety and Effect on Memory of PYM50028 in Mild Alzheimer's Disease

NCT00130429 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2009-08-21

No results posted yet for this study

Summary

The purpose of this study is to assess the effect of PYM50028 administered once daily for up to 12 weeks on the memory and other faculties of subjects with dementia due to Alzheimer's disease.

Conditions

Interventions

DRUG

PYM50028

Sponsors & Collaborators

  • Phytopharm

    lead INDUSTRY

Principal Investigators

  • Robin Jacoby, FRCPsych · University of Oxford, UK

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-01-31
Completion
2005-09-30

Countries

  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00130429 on ClinicalTrials.gov