Molecular structure of memantine
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Memantine

Memantine is the first in a novel class of Alzheimer's disease medications acting on the glutamatergic system. Memantine was developed by Merz and licensed to Forest for the U.S. and Lundbeck for selected European and international markets. Memantine is marketed under the brands Axura and Akatinol by Merz, Namenda by Forest and Ebixa by Lundbeck. more...

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Pharmacology

NMDA receptor

A dysfunction of glutamatergic neurotransmission, manifested as neuronal excitotoxicity, is involved in the aetiology of Alzheimer's disease. Targeting the glutamatergic system, specifically NMDA receptors, offers a novel approach to treatment in view of the limited efficacy of existing drugs targeting the cholinergic system. (Cacabelos et al., 1999)

Memantine is a low-affinity voltage-dependent uncompetitive antagonist at glutamatergic NMDA receptors. By binding to the NMDA receptor with a higher affinity than Mg2+ ions, memantine is able to inhibit the prolonged influx of Ca2+ ions which forms the basis of neuronal excitotoxicity. The low-affinity of memantine, however, preserves the physiological function of the receptor as it can still be activated by the relatively high concentrations of glutamate released following depolarisation of the presynaptic neuron.

5-HT3

Memantine acts as an uncompetitive antagonist at the 5HT3 receptor, with a potency similar to that for the NMDA receptor. (Rammes et al., 2001) The clinical significance of this serotonergic activity in the treatment of Alzheimer's disease is unknown.

Clinical use

Indications

Memantine is indicated for the treatment of the symptoms of moderate to severe Alzheimer's disease. (Joint Formulary Committee, 2004; Rossi, 2006)

Memantine has been associated with a moderate decrease in clinical deterioration in Alzheimer's disease. (Rossi, 2006) A systematic review of randomised controlled trials found that memantine has a small positive effect on cognition, mood, behaviour, and the ability to perform daily activities in moderate to severe Alzheimer's disease, but an unknown effect in mild to moderate disease. (Areosa et al., 2005)

Memantine is also being tested for depression, glaucoma, and neuropathic pain.

Adverse drug reactions

Memantine is generally well-tolerated. (Areosa et al., 2005) Common adverse drug reactions (ADRs) include: confusion, dizziness, drowsiness, headache, insomnia, agitation, and hallucinations. (Rossi, 2006) Less common ADRs include: vomiting, anxiety, hypertonia, cystitis, and increased libido. (Joint Formulary Committee, 2004)

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Merz + Co./Forest Labs Sign Pact For Memantine Development
From Worldwide Biotech, 8/1/00

Neurobiological Technologies, Inc. (NTI*) (OTC-BB:NTII), Richmond, Calif., has announced that its corporate collaborator, Merz + Co. (http://www.merz.de/index_ehtml) of Frankfurt, Germany has entered into an agreement with Forest Laboratories, Inc. (NYSE: FRX), for the development and marketing of Memantine in the United States for the treatment of Alzheimer's disease, neuropathic pain, and AIDS-related dementia.

Memantine is the leading prescription pharmaceutical product used in the treatment of dementia in Germany. Merz has completed three separate Phase III clinical trials of Memantine for mild to moderate vascular dementia, moderately severe to severe dementia, and Alzheimer's disease in Europe. In February 2000, Merz announced positive results after completing a Phase III trial in the U.S. for moderately severe to severe Alzheimer's disease. The U.S. study demonstrated improvement in patients with more advanced disease for which no other treatment has yet proven successful.

NTI recently completed a 421-patient, Phase IIB clinical trial in the U.S. of Memantine for diabetic neuropathic pain that demonstrated a statistically significant reduction in nighttime pain after treatment with Memantine. In addition, last January NTI completed enrollment in a double-blind, placebo-controlled Phase II clinical trial of Memantine for AIDS-related dementia funded by the National Institute of Health (NIH) and conducted by the AIDS Clinical Trials Group (ACTG), a clinical consortium funded by the National Institute of Allergy and Infectious Diseases (NIAID). The company expects results of this trial to be reported in the latter part of this year.

Memantine is an orally active N-methyl-D-aspartate (NMDA) antagonist. Research indicates that NMDA receptor antagonists have the potential to prevent the injury and death of neurons related to a variety of conditions, including neuropathic pain, Alzheimer's disease, Huntington's disease, and AIDS-related dementia. Memantine is the first NMDA receptor antagonist to show efficacy in Alzheimer's disease and vascular dementia.

"NTI is delighted that Merz + Co., our corporate collaborator on Memantine, and Forest Laboratories have entered into this agreement for the development and marketing of Memantine in the U.S.," said Paul E. Freiman, president and chief executive officer of NTI. "This agreement will initiate a sharing of payments with Merz on a formula basis including front-end, milestone and royalty payments. We strongly believe that Memantine will be an important and successful treatment for a number of NMDA-receptor-related neurological diseases."

NTI is an emerging drug development company focused on the clinical evaluation and regulatory approval of neuroprotective drugs. The company's strategy is to in-license and develop early-stage drug candidates that target major medical needs and that can be rapidly commercialized. NTI is currently developing Memantine for multiple neurological conditions and evaluating XERECEPT* as a treatment for peritumoral brain edema.

For more information, call 415-974-7230.

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