Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease wh
ich was thought to be untreatable for a long time. However, recent evidence
in men indicates that antiglutamatergic strategies are the first to have a
n influence on its pathogenesis and slow down the disease process. Since th
e effect of the drugs is still small, this progress cannot only be seen as
a success of the present but most also be acknowledged as a starting point
for the future. How will these future studies look like? They will have to
take into account that ALS presumably has a long preclinical period and the
y will use a number of novel compounds and treatment strategies which have
recently been shown to be effective in a transgenic animal model. This also
implies that we are likely to use combination therapies and have to try to
treat patients early. The latter will be necessarily connected with the de
mand for a novel clinical attitude to the diagnosis of the disease.