Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease resulting in increasing disability,being uniformly fatal. Since its approval in the 1990s, riluzole remained for long time the unique treatment, offeringmodest survival benefit. Most recently a second drug has been approved by the US Food and Drug Administrationfor treatment of ALS: edaravone. Significant advances have been made in the symptomatic management of thedisease but more effective drug therapy targeting disease progression is still dreadfully needed, the success appearing almost a miracle. Recent discoveries related to genetics indicate divergent mechanisms of disease encouraging precision medicine leading to molecularly tailored interventions. The search for effective therapy still faces important challenges in the areas of both basic science and animal research, adequate translation of results into human clinical trials, inherent bias in human studies, and issues related to delays in clinical diagnosis. It is interesting to point out that ALS research may speed up drug development not only for this disease, but also forother more prevalent neurodegenerative diseases: the reverse is also conceivable.
Therapy in Amyotrophic Lateral Sclerosis (ALS) : an unexpected evolving scenario / V. Silani. - In: ARCHIVES ITALIENNES DE BIOLOGIE. - ISSN 0003-9829. - 155:4(2017), pp. 228-241. [10.12871/00039829201747]
Therapy in Amyotrophic Lateral Sclerosis (ALS) : an unexpected evolving scenario
V. Silani
2017
Abstract
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease resulting in increasing disability,being uniformly fatal. Since its approval in the 1990s, riluzole remained for long time the unique treatment, offeringmodest survival benefit. Most recently a second drug has been approved by the US Food and Drug Administrationfor treatment of ALS: edaravone. Significant advances have been made in the symptomatic management of thedisease but more effective drug therapy targeting disease progression is still dreadfully needed, the success appearing almost a miracle. Recent discoveries related to genetics indicate divergent mechanisms of disease encouraging precision medicine leading to molecularly tailored interventions. The search for effective therapy still faces important challenges in the areas of both basic science and animal research, adequate translation of results into human clinical trials, inherent bias in human studies, and issues related to delays in clinical diagnosis. It is interesting to point out that ALS research may speed up drug development not only for this disease, but also forother more prevalent neurodegenerative diseases: the reverse is also conceivable.File | Dimensione | Formato | |
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