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Bexicaserin (LP352) in Participants with Developmental and Epileptic Encephalopathies (DEES)","therapeuticArea":"Neurology","highestDevelopmentStatus":"Phase II","country":"U.S.A","productType":"Small molecule","productStatus":"New Molecular Entity","date":"January 2024","url1":"","url2":"","graph1":"Neurology","graph2":"Phase II"},{"orgOrder":0,"company":"Longboard Pharmaceuticals","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"Longboard Pharmaceuticals Announces Initiation of First-in-Human Phase 1 Clinical Study of LP659 in Adult Healthy Volunteers","therapeuticArea":"Rare Diseases and Disorders","highestDevelopmentStatus":"Phase I","country":"U.S.A","productType":"Small molecule","productStatus":"New Molecular Entity","date":"November 2023","url1":"","url2":"","graph1":"Rare Diseases and Disorders","graph2":"Phase I"}]
Find Clinical Drug Pipeline Developments & Deals by Longboard Pharmaceuticals
The proceeds will advance research and development and clinical trial expenses of company's pipeline including LP352 (bexicaserin), an oral, centrally acting, 5-HT2C superagonist for seizures associated with DEEs such as Dravet syndrome and Lennox-Gastaut syndrome.
The net proceeds will advance research and development expenses, clinical trial expenses of company's pipeline including LP352, an oral, centrally acting, 5-HT2C superagonist in development for seizures associated with DEEs such as Dravet syndrome and Lennox-Gastaut syndrome.
The net proceeds will advance research and development expenses, clinical trial expenses of company's pipeline including LP352, an oral, centrally acting, 5-HT2C superagonist in development for seizures associated with DEEs such as Dravet syndrome and Lennox-Gastaut syndrome.
LP352 (Bexicaserin) is a potentially best-in-class and highly selective, oral, novel 5-HT2C receptor superagonist, which is under phase 1/2 clinical development for the treatment of Developmental and Epileptic Encephalopathies (DEEs).
LP352 (Bexicaserin) is a potentially best-in-class and highly selective, oral, novel 5-HT2C receptor superagonist, which is under phase 1/2 clinical development for the treatment of Developmental and Epileptic Encephalopathies (DEEs).
LP659 is a S1P1/5 receptor Modulator, small molecule drug, which is currently being investigated for the treatment of rare neuroinflammatory conditions.
LP352 is an oral, centrally acting, 5-HT2C superagonist in development for the potential treatment of seizures associated with DEEs such as Lennox-Gastaut syndrome (LGS), tuberous sclerosis complex (TSC), CDKL5 deficiency disorder (CDD), and other epileptic disorders.
The agreement spans a range of Societal CDMO’s offerings including technology transfer and analytical method validation activities to support Longboard’s Oral, Centrally Acting 5-HT2C Receptor Superagonist, LP352, being developed for treatment of refractory seizures.
The Company expects to use the net proceeds from the Offering, for the advancement of the Company’s clinical development programs, including LP352 and for working capital and other general corporate purposes.
The Company intends to use the net proceeds from the offering primarily for the acceleration of the development of LP352, and supporting business development activities, and for general corporate purposes.