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NCT00809510

A Study of the Long-term Safety of ABT-089 for Subjects With Mild-to-moderate Alzheimer's Disease Who Participated in the M06-876 Study

Terminated Phase 2 Last updated 1 September 2011
What this trial tests

Phase 2 trial testing ABT-089 in Alzheimer's Disease in 63 participants. Terminated before completion.

Timeline
1 January 2009
Primary endpoint
1 June 2009

Quick facts

Lead sponsorAbbott
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment63
Start date1 January 2009
Primary completion1 June 2009
Sites22 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Abbott — full company profile →

Who can join

Adults 55 to 90, any sex, with Alzheimer's Disease. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to evaluate the long-term safety and tolerability of ABT-089 in adults with mild-to-moderate Alzheimer's disease.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. A Systematic Review on Drugs Acting as Nicotinic Acetylcholine Receptor Agonists in the Treatment of Dementia.
    Crestini A, Carbone E, Rivabene R, Ancidoni A, et al · · 2024 · cited 11× · PMID 38334629 · DOI 10.3390/cells13030237

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Other recruiting trials for Alzheimer's Disease

Currently open trials in the same condition.

Other Abbott trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00809510.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing