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The Safety and Efficacy of Neramexane in Patients With Moderate to Severe Alzheimer's Disease

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Forest Laboratories

Status and phase

Completed
Phase 3

Conditions

Alzheimer's Disease

Treatments

Drug: Neramexane

Study type

Interventional

Funder types

Industry

Identifiers

NCT00090116
NER-MD-02

Details and patient eligibility

About

Memory loss and difficulties with thinking associated with Alzheimer's disease may be due to chronic release of a brain chemical called glutamate. Glutamate helps transmit messages between nerve cells through interaction with a certain type of receptor (N-methyl-D-aspartate, NMDA) on the cell. Neramexane is a new drug that blocks the effects of excessive glutamate at the receptor (NMDA receptor antagonist).

Sex

All

Ages

50+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinical diagnosis of moderate to severe Alzheimer's disease;
  • ambulatory patients

Exclusion criteria

  • folate deficiency;
  • clinically significant central nervous system disease other than Alzheimer's disease;
  • clinically significant pulmonary, gastrointestinal, renal, hepatic, endocrine or cardiovascular disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

35

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Data sourced from clinicaltrials.gov

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