Ontology highlight
ABSTRACT: Background/objective
Amyotrophic lateral sclerosis (ALS) is a diagnosis that incorporates a heterogeneous set of neurodegenerative processes into a single progressive and uniformly fatal disease making the development of a uniformly applicable therapeutic difficult. Recent multinational ALS natural history incidence studies have identified systemic chronic activation of the innate immune system as a major risk factor for developing ALS. Persistent immune activation in patients with ALS leads to loss of muscle and lowering of serum creatinine. The goal of the current study was to test whether the slowing of nerve and muscle destruction in NP001-treated ALS patients compared with controls in phase 2 studies would lead to extension of survival.Methods
Phase 2 clinical studies
SUBMITTER: McGrath MS
PROVIDER: S-EPMC11505581 | biostudies-literature | 2024 Oct
REPOSITORIES: biostudies-literature