Monoclonal antibody | |
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Type | Whole antibody |
Source | Humanized |
Target | Beta amyloid |
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Formula | C6396H9922N1712O1996S42 |
Molar mass | 144.1 kg/mol |
(what is this?) |
Solanezumab (proposed INN, LY2062430) is a monoclonal antibody being investigated by Eli Lilly as a neuroprotector for patients with Alzheimer's disease. The drug originally attracted extensive media coverage proclaiming it a breakthrough, but it has failed to show promise in Phase III trials.
Solanezumab was safely used in combination with approved Alzheimer’s disease treatment, such as acetylcholinesterase inhibitors or memantine, in the clinical trials.
Aside from Alzheimer’s disease, there are other amyloid beta related diseases, in which solanezumab could be used, e.g., Down syndrome or cerebral amyloid angiopathy. However, this has not been studied so far.
No safety concerns were detected in any of the studies. A few patients suffered from mild infusion reactions that resolved on their own. The measured laboratory values and vital signs, showed no changes. Other adverse events that occurred, e.g., headache or hematoma, where not considered as related to treatment.
Other anti-amyloid beta antibodies caused amyloid-related imaging abnormalities, which is not the case for solanezumab.
Solanezumab binds the amyloid-β peptides that aggregate and form plaques in the brain that are an early pathological feature of Alzheimer's disease. Solanezumab binds the central epitope of monomeric amyloid-β, KLVFFAD, (PDB ID 4XXD) with picomolar affinity. This epitope is known as the nucleation site for Aβ oligomerization, and it is these oligomers of Aβ that are thought to be toxic to neurons.