Forest's Namenda becomes first FDA-approved therapy for advanced AD
The US Food and Drug Administration has approved the use of ForestLaboratories' Namenda (memantine) for the treatment of patients with moderate-to-severe Alzheimer's disease. Forest obtained the exclusive development and commercialization rights to the agent from Merz Pharmaceuticals in July 2000 (Marketletters passim).
Indicated for advanced AD
The number of AD sufferers is estimated to be four million in the USA and 15 million worldwide, and Namenda becomes the first drug registered by the FDA for the moderate-to-severe form of the condition, noted the company.
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