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A Study Of PF-04447943 Compared To Placebo In Subjects With Mild To Moderate Alzheimer's Disease

Pfizer logo

Pfizer

Status and phase

Completed
Phase 2

Conditions

Alzheimer's Disease

Treatments

Drug: PF-04447943
Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT00930059
B0401005
2009-012179-82 (EudraCT Number)

Details and patient eligibility

About

The purpose of this study is to evaluate the effects of PF-04447943 compared to placebo on cognitive, behavioral and overall symptoms of Alzheimer's disease; evaluate the safety and tolerability of PF-0444793 compared to placebo; and determine the levels of PF-04447943 in the plasma over the course of the study.

Enrollment

191 patients

Sex

All

Ages

55 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Mild to moderate Alzheimer's disease (MMSE 14-26)
  • Good general health (such controlled conditions as Type 2 diabetes and hypertension allowed)

Exclusion criteria

  • Use of acetylcholinesterase inhibitors (donepezil, rivastigmine, or galantamine) or memantine within 12 weeks of the start of the study
  • Significant cardiovascular disease in the past 6 months
  • Illness other than Alzheimer's disease that could contribute to cognitive impairment
  • History of stroke or seizure disorder

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

191 participants in 2 patient groups, including a placebo group

PF-04447943
Experimental group
Treatment:
Drug: PF-04447943
Placebo
Placebo Comparator group
Treatment:
Drug: Placebo

Trial contacts and locations

45

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Data sourced from clinicaltrials.gov

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