Fission Pharma is developing a protein-protein interaction inhibitor drug that cuts the link between chronic inflammation and mitochondrial dysfunction to treat multiple age-related and neurodegenerative diseases to extend human lifespan. Referenced from VitaDAO VDP-143
P110 peptide has been shows to improve disease-specific phenotypes in mouse models of ALS, AD, Huntington Disease
(from VDP-143 referenced above) Fission Pharma is creating the first drug-like small molecule P110 mimetics. P110 is a mito-protective peptide originating from Stanford University [1]. The efficacy of P110 in treating neurodegenerative and cardiac disease is supported by 13 years of research, resulting in 20 scientific publications across 11 disease models and collaboration with 15 independent labs globally. P110 has highly generalized anti-degenerative activity, increasing lifespan in mouse models of neurodegeneration (HD [2-5], ALS [5-6], AD [5, 7, 8], PD [1], MS, stroke, and scrapie) and also a model of ischemic heart disease [9]. Dr. Luis Rios published the first small molecule P110 mimetics in 2023 [10] and showed comparable efficacy to P110 in mouse models of ALS and sepsis. These inhibitors have a unique property, they inhibit the downstream pathological consequences of inflammation without inhibiting immune signals. These compounds aim to be the first effective and generalized orally available and brain penetrant treatments for chronic inflammation and mitochondrial dysfunction, critical hallmarks of aging, and may do so without causing immunosuppression, the limiting factor in chronic inflammation treatment. The most tractable go-to-market strategy will be in a rare neurodegenerative disease (ALS) and they will expand to age-related degenerative indications such as AD and ischemic heart disease, the major limiting factors in human lifespan.
Cerebrum DAO Neuroscience Deal Flow group has recommended the proposal for funding with the following conditions: co-funding the company-building project, initiated and funded with $250,000 from VitaDAO for 60% of the IP-NFT and $83,333 from Cerebrum DAO in exchange for the 20% share of the resulting IP-NFT.
The funding should be transferred in tranches, based on the milestones. As the result, the project should move from PRL 2 (validated hypothesis in animal studies) to PRL 4 (Initial hits identified, leads are effective in the secondary screen in neurons).