Preliminary Efficacy and Safety Study of ST101 in Alzheimer's Disease

Phase 2

Completed

• Conditions: Alzheimer's Disease
• Interventions: Drug: ST101; Drug: Placebo

• Registration Number: NCT00842673
• Lead Sponsor: Sonexa Therapeutics, Inc.

Brief Summary

This study will investigate the ability of ST101 to improve memory in people with Alzheimer's disease. This study also will examine the safety and tolerability of the drug. This study is evaluating 3 different dose levels of ST101 and placebo. Patients will have a 1 in 4 chance of getting placebo.

Detailed Description

Alzheimer's disease (AD) is a progressive and fatal neurological illness. It produces changes in the brain that include loss of cells and accumulation of abnormal protein deposits. Initial symptoms are cognitive, with deficiencies in short-term memory the most common symptom. As the disease progresses so does the severity of cognitive deficiency. Loss of speech and immobility occur in the terminal stages There is no cure for AD and no marketed treatment that modifies the underlying disease process. Available therapies improve some symptoms of AD by increasing brain concentrations of molecules involved in cognition. ST101 differs from marketed therapies in that it has demonstrated two actions in animal research testing. It improves cognition and it also reduces the accumulation of abnormal protein deposits in the brain. These two properties suggest that ST101 may be a promising agent for the treatment of AD. This study is designed as a preliminary dose exploration/proof-of-concept investigation of the ability of ST101 to improve cognition during 12 weeks of administration.

Study Timeline

• Study Start: 2009-02
• Study First Submitted: 2009-02-10
• Study First Submitted QC: 2009-02-10
• Study First Posted: 2009-02-12
• Primary Completion: 2010-09
• Study Completion: 2010-09
• Status Verified: 2012-06
• Last Update Submitted: 2012-06-05
• Last Update Posted: 2012-06-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 168

Inclusion Criteria

• Diagnostic evidence of mild to moderate Alzheimer's disease.
• CT or MRI results within the past 12 months that rule out dementia due to non-Alzheimer's etiology.
• A reliable and capable caregiver.

Exclusion Criteria

• Subjects who reside in a skilled nursing facility.
• Subjects with B12 or folate deficiency.
• Subjects with chronic hepatic disease.
• Subjects with a recent history of hematologic/oncologic disorders.
• Subjects who have experienced a myocardial infarction with the past year.
• Dementia caused or complicated by other organic disease

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	ST101	30 mg ST101
2	ST101	90 mg ST101
3	ST101	180 mg ST101
4	Placebo	Placebo

Primary Outcome Measures

Name	Time	Method
Alzheimer's Disease Assessment Scale, Cognitive Subscale (ADAS-cog)	Baseline, 4 weeks, 8 weeks,12 weeks

Secondary Outcome Measures

Name	Time	Method
Alzheimer's Disease Cooperative Study - Activities of Daily Living (ADCS-ADL)	Baseline, 4 weeks, 8 weeks, 12 weeks
Neuropsychiatric Inventory (NPI)	Baseline, 4 weeks, 8 weeks, 12 weeks
Alzheimer's Disease Cooperative Study- Clinical Global Impression (ADCS-CGI)	Baseline (severity); 4 weeks, 8 weeks, 12 weeks (change)