| Literature DB >> 34229081 |
Abstract
In 2020, the anti-tumor necrosis factor (TNF) monoclonal antibody Humira® generated US$165.8 billion in cumulative sales and snatched the crown for the industry's most successful drug from Lipitor (atorvastatin). TNF-α is a major component in beneficial and disease-related inflammation and TNF-α-inhibitor biologics have gained widespread use in autoimmune diseases, such as rheumatoid arthritis (RA). Many more diseases could benefit from TNF-α inhibitors, such as Alzheimer's disease (AD) or major depression. However, the nature of TNF-α-inhibitor biologics prohibits central nervous system (CNS) applications. Moreover, high drug production costs and pricing, together with antidrug immune reactions and insufficient patient coverage, argue for the development of small-molecule drugs. Recently, drug-like orally available small molecules were described with high activity in animal disease models with activities comparable to those of antibodies.Entities:
Keywords: Antagonist; Antibody; Inflammation; Protein/protein interaction; Small molecule; Structure-based design; Symmetry disruption; TNF-α; TNF-α receptor
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Year: 2021 PMID: 34229081 DOI: 10.1016/j.drudis.2021.06.018
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851