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Search / Trial NCT02337907

BI 409306 in Patients With Cognitive Impairment Due to Alzheimer's Disease.

Launched by BOEHRINGER INGELHEIM · Jan 9, 2015

Trial Information

Current as of August 11, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion criteria:
  • Patients with early signs of dementia of Alzheimer Type
  • Male and female patients with an age of at least 55 years
  • Previous use of Alzheimer's Disease (AD) medications (AChEIs, memantine) is allowed up 3 month prior to screening. Patients who are currently taking AChEIs are eligible as long as they have been using a stable dose for at least 3 months prior to screening and no change is foreseen for the duration of the study. This dose must be consistent with the product label in the concerned country. Patients currently taking memantine are excluded.
  • Patients must have at least 6 years of formal education and fluency in the test language as verbally confirmed by the patient and documented by the study investigator.
  • Patients must have a reliable study partner (per investigator judgement, for instance a family member, partner etc., guardian or, if applicable, a legal representative)
  • Exclusion criteria:
  • Cognitive impairment or dementia with any etiology other than Alzheimer's Disease (AD)
  • Substantial concomitant cerebrovascular disease (defined by a history of a stroke / intracranial haemorrhagia) temporally related to the onset of worsening of cognitive impairment per investigator judgement
  • Medical history or diagnosis of any of symptomatic and unstable/uncontrolled conditions per investigator judgement
  • Any other psychiatric disorders such as schizophrenia, or mental retardation
  • Previous participation in investigational drug studies of mild cognitive impairment/Dementia of Alzheimer Type (DAT) within three months prior to screening. Having received active treatment in any other study targeting disease modification of AD like Aß immunization and tau therapies. Previous participation in studies with non-prescription medications, vitamins or other nutritional formulations is allowed.
  • Clinically significant uncompensated hearing loss in the judgment of the investigator. Use of hearing aids is allowed.

About Boehringer Ingelheim

Boehringer Ingelheim is a global, research-driven pharmaceutical company dedicated to improving health and quality of life through innovative therapies. Established in 1885 and headquartered in Ingelheim, Germany, the company focuses on the development of prescription medicines in key therapeutic areas, including respiratory diseases, cardiovascular health, oncology, and immunology. Boehringer Ingelheim is committed to advancing medical science through rigorous clinical trials and collaborative research, striving to bring novel treatments to patients while upholding the highest standards of safety and efficacy. With a strong emphasis on sustainability and corporate responsibility, the company aims to make a meaningful impact on global health challenges.

Locations

West Palm Beach, Florida, United States

Indianapolis, Indiana, United States

Regina, Saskatchewan, Canada

Bath, , United Kingdom

Bennington, Vermont, United States

Ulm, , Germany

Staten Island, New York, United States

Berlin, , Germany

Calgary, Alberta, Canada

Tulsa, Oklahoma, United States

Dendermonde, , Belgium

Eatontown, New Jersey, United States

Firenze, , Italy

Mannheim, , Germany

Mainz, , Germany

Gent, , Belgium

Penticton, British Columbia, Canada

Amadora, , Portugal

Coimbra, , Portugal

Santa Maria Da Feira, , Portugal

Bologna, , Italy

'S Hertogenbosch, , Netherlands

Dijon, , France

Orlando, Florida, United States

Braga, , Portugal

Sherman Oaks, California, United States

Parma, , Italy

Loures, , Portugal

Brussel, , Belgium

Bochum, , Germany

Bordeaux, , France

Lisboa, , Portugal

Charlotte, North Carolina, United States

Wien, , Austria

Quebec, , Canada

Montpellier, , France

Nantes, , France

Paris, , France

Poitiers, , France

Berlin, , Germany

Leipzig, , Germany

Westerstede, , Germany

Amsterdam, , Netherlands

Kielce, , Poland

Poznan, , Poland

Sopot, , Poland

Szczecin, , Poland

Wroclaw, , Poland

Plymouth, , United Kingdom

Rochester, New York, United States

Mons, , Belgium

Marseille, , France

Erbach, , Germany

Bialystok, , Poland

Lublin, , Poland

Lublin, , Poland

Guimarães, , Portugal

Matosinhos, , Portugal

Dundee, Scotland, , United Kingdom

Ivybridge, , United Kingdom

Patients applied

0 patients applied

Trial Officials

Boehringer Ingelheim

Study Chair

Boehringer Ingelheim

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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