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Reunion Neuroscience Appoints Robert Alexander as Chief Medical Officer

Reunion Neuroscience Appoints Robert Alexander as Chief Medical Officer
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Oral Orexin Agonist Gets Breakthrough Therapy Status for Narcolepsy Type 1

Oral Orexin Agonist Gets Breakthrough Therapy Status for Narcolepsy Type 1
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Redirecting to U.S. Food and Drug Administration Grants Breakthrough Therapy Designation to Takeda's Investigational Compound, TAK-994, an Oral Orexin Agonist in Clinical Development for Narcolepsy Type 1 (NT1)

Redirecting to U.S. Food and Drug Administration Grants Breakthrough Therapy Designation to Takeda's Investigational Compound, TAK-994, an Oral Orexin Agonist in Clinical Development for Narcolepsy Type 1 (NT1)
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Global Roundup: Takeda and PeptiDream Expand CNS Collaboration

Global Roundup: Takeda and PeptiDream Expand CNS Collaboration
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Redirecting to Takeda Secures Global Rights from Ovid Therapeutics to Develop and Commercialize Soticlestat for the Treatment of Children and Adults with Dravet Syndrome and Lennox-Gastaut Syndrome

March 5, 2021 healthcare Takeda Secures Global Rights from Ovid Therapeutics to Develop and Commercialize Soticlestat for the Treatment of Children and Adults with Dravet Syndrome and Lennox-Gastaut Syndrome − Ovid eligible to receive up to $856M in payments, including a $196M upfront payment, regulatory and commercial milestone payments and tiered double-digit royalties on product sales − Potential first-in-class therapy reduced seizure frequency in children with Dravet syndrome and Lennox-Gastaut syndrome in Phase 2 ELEKTRA study − Original 2017 collaboration between Ovid and Takeda to conclude; Ovid will have no further development or milestone obligations − Takeda plans to initiate Phase 3 studies in children and adults with Dravet syndrome and Lennox-Gastaut syndrome in calendar year Q2 2021

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Ovid-therapeutics

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