Efficacy in Alzheimer's disease

An efficacious treatment for moderate to severe Alzheimer’s disease

Meta-analyses of six Phase III, placebo-controlled, 6-month studies in AD patients with MMSE <20 (memantine 29 mg/day, ITT (Intent To Treat), OC (Observed Cases)).
  • A meta analysis from six Phase III, placebo-controlled, 6-months studies showed that there was a statistically significant effect in favour of Ebixa (memantine) treatment for the cognitive, global, and functional domains.
  • The analysis included 1,826 patients with moderate to severe Alzheimer's disease (MMSE <20) (ref.1).

Significant effect of Ebixa in preventing marked clinical worsening in moderate to severe Alzheimer's disease (ref.2)

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***p<0.001
  • Prevention of clinical worsening is a relevant and realistic treatment goal in Alzheimer’s disease. Ebixa has shown a statistical significant effect in preventing concurrent clinical worsening in all three domains; cognitive, global and functional domains. Twice as many placebo treated patients showed worsening in all three domains compared to Ebixa (mematine) (Placebo 21% vs. memantine 11%, p<0.0001)
  • The analysis included 1,826 patients with moderate to severe Alzheimer’s disease (MMSE < 20)

References:

1. Winblad B, Jones RW, Wirth Y, Stoffler A, Mobius HJ. Memantine in Moderate to Severe Alzheimer's Disease: a Meta-Analysis of Randomised Clinical Trials. Dement Geriatr Cogn Disord 2007; 24(1):20-27.

2. Wilkinson D, Andersen HF. Analysis of the effect of memantine in reducing the worsening of clinical symptoms in patients with moderate to severe Alzheimer's disease. Dement Geriatr Cogn Disord 2007; 24(2):138-145.

Last updated: 03.09.2007