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NCT00414622 Clinical Trial

GTS21-201 for Alzheimer Disease:GTS-21 Administered Daily for 28 Days to Participants With Probable Alzheimer’s Disease

Alzheimer Disease Clinical Trial

Official title:
A Double Blind, Placebo-Controlled Randomized Study to Compare the Safety and Tolerability of GTS-21 (25 Mg TID, 50 Mg TID, 75 Mg TID and 150 Mg TID) When Administered Daily for 28 Days to Participants With Probable Alzheimer’s Disease

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00414622
Other study ID # GTS21-201
Secondary ID
Status Completed
Phase Phase 2
First received December 19, 2006
Last updated April 18, 2007
Start date November 2006
Est. completion date April 2007

Study information
Verified date December 2006
Source CoMentis
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A Double Blind, Placebo-Controlled Randomized Study to Compare the Safety and Tolerability of GTS-21 (25 Mg TID, 50 Mg TID, 75 Mg TID and 150 Mg TID) When Administered Daily for 28 Days to Participants With Probable Alzheimer’s Disease

Description:

A Double Blind, Placebo-Controlled Randomized Study to Compare the Safety and Tolerability of GTS-21 (25 Mg TID, 50 Mg TID, 75 Mg TID and 150 Mg TID) When Administered Daily for 28 Days to Participants With Probable Alzheimer’s Disease

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date April 2007
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria:

- probable Alzheimer

Exclusion Criteria:

- others

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• DMXB-A

Locations
Country Name City State
United States Clinical Dept. 280 South San Francisco California

Sponsors (1)
Lead Sponsor Collaborator
CoMentis

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary CDR
Secondary ADAS-cog
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