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Valent BioSciences and Kansas State University Sign Collaborative Agreement for Soil Health Research Initiative with Dr. Charles W. Rice
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Sunovion Marks 10 Years of Addressing Serious Medical Conditions That Impact the Lives of Millions Worldwide
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Sunovion Announces the Commercial Launch of KYNMOBI™ (apomorphine hydrochloride) Sublingual Film for the Treatment of Parkinson’s Disease OFF Episodes
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Sunovion Answers Is Named a J.D. Power 2020 Certified Customer Service ProgramSM
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Myovant Sciences Announces Further Financing Support from Sumitomo Dainippon Pharma and Commercial Collaboration with Sunovion Pharmaceuticals
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Sunovion Announces Topline Results from Global Phase 2 Study of SEP-4199 in Patients with Bipolar I Depression
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AMSA and Sunovion Team Up For Second Year of Neuroscience Peer Teaching Program While Transitioning to Remote Learning Experience
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Sunovion Announces Health Canada Approval of KYNMOBI™ (apomorphine hydrochloride) Soluble Film for the Treatment of Parkinson’s Disease OFF Episodes
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Sunovion Announces U.S. FDA Approval of KYNMOBI™ (apomorphine hydrochloride) Sublingual Film for the Treatment of Parkinson’s Disease OFF Episodes
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Sunovion Discontinues Dasotraline Program
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New England Journal of Medicine Publishes Pivotal Results Evaluating Sunovion’s SEP-363856 for the Treatment of Schizophrenia
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Myovant Sciences Announces Closing of $400 Million Loan Facility, Repayment of Debt, Board of Director Transitions, and Executive Promotions
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Sunovion Announces FDA Filing Acceptance of Resubmitted New Drug Application for Apomorphine Sublingual Film
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Sunovion Announces Results from Its Open-Label Extension Study of SEP-363856 in Schizophrenia
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Actor and Advocate Chyler Leigh and the American Foundation for Suicide Prevention Join Be Vocal: Speak Up for Mental Health Initiative
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Sunovion Resubmits New Drug Application for Apomorphine Sublingual Film
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Sunovion President and CEO Dr. Antony Loebel Receives Outstanding Leadership Award at CNS Summit
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Myovant Sciences Enters Landmark Agreement with Sumitomo Dainippon Pharma to Secure Major Financial Backing and Safeguards for Minority Shareholders
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Sunovion Answers Becomes a J.D. Power 2019 Certified Customer Service Program℠
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Sunovion and PsychoGenics Initiate DIAMOND Phase 3 Clinical Studies for SEP-363856 in the Treatment of Adults and Adolescents with Schizophrenia
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Myovant Sciences’ Founding Shareholder Roivant Sciences, and Sumitomo Dainippon Pharma Enter into a Memorandum of Understanding to Create a Broad Strategic Alliance
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Sunovion Receives 2018 Corporate Responsibility and Leadership Awards from United Way of Tri-County and Expands Partnership For 8th Annual Community Service Program
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Sunovion Announces Acceptance by the U.S. FDA of the New Drug Application for Dasotraline for the Treatment of Adults with Moderate-to-Severe Binge Eating Disorder
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AMSA and Sunovion Partner to Inspire Next Generation of Innovators, Provide Students With Opportunity to Teach Neuroscience to Their Classmates
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Sunovion and PsychoGenics Announce that SEP-363856 Has Received FDA Breakthrough Therapy Designation for the Treatment of People with Schizophrenia
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Sunovion Highlights Data from Its Psychiatry Portfolio at the 2019 American Psychiatric Association Annual Meeting
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Sunovion to Present Data on LONHALA® MAGNAIR® Inhalation Solution and COPD at the American Thoracic Society International Conference 2019
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Sunovion Announces Appointment of Dr. Antony Loebel as President and CEO, Effective April 1, 2019
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Sunovion Receives Complete Response Letter from FDA for Apomorphine Sublingual Film (APL-130277)
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Sunovion and PsychoGenics Announce Positive Results from Pivotal Phase 2 Study of Novel Investigational Agent SEP-363856 for the Treatment of Schizophrenia
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Sunovion Announces Health Canada Approval of Aptiom® (eslicarbazepine acetate) as Adjunctive Therapy for the Treatment of Partial-Onset Seizures in Adolescents and Children Above Six Years of Age
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Sunovion Announces Health Canada Approval of Aptiom® (eslicarbazepine acetate) as Adjunctive Therapy for the Treatment of Partial-Onset Seizures in Adolescents and Children Above Six Years of Age
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Sunovion Announces Health Canada Acceptance of New Drug Submission for Apomorphine Sublingual Film (APL-130277)
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FDA Issues a Complete Response Letter for New Drug Application for Dasotraline for the Treatment of ADHD
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Tolero Pharmaceuticals Announces Clinical Research Collaboration with AbbVie for Acute Myeloid Leukemia Trial
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Sunovion Announces Positive Top-Line Results from Pivotal Study Evaluating Dasotraline in Adults with Binge Eating Disorder
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Sunovion to Launch Take On Tomorrow™ Giving Opportunity with Red Sox Foundation and 7th Annual Community Service Program
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Sunovion Announces Health Canada Approval of Aptiom® (eslicarbazepine acetate) as Monotherapy to Treat Partial-Onset Seizures in Adults with Epilepsy
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Sunovion Presents Data from Pivotal Phase 3 Study of Apomorphine Sublingual Film (APL-130277) at the 2nd Pan American Parkinson’s Disease and Movement Disorders Congress
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Sunovion Announces FDA Acceptance of New Drug Application for Apomorphine Sublingual Film (APL-130277)
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Sunovion Announces Data Presentations Highlighting Broad Portfolio of Treatments for COPD at the American Thoracic Society International Conference 2018
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Sunovion Answers Becomes a J.D. Power 2017 Certified Contact Center
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Sunovion to Deliver Multiple Presentations at the 2018 American Psychiatric Association Annual Meeting
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Sunovion Announces Health Canada Approval of Latuda® (lurasidone HCl) to Treat Adolescents (13 to 17 years of age) with Bipolar Depression
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Sunovion Announces Lonhala™ Magnair™ (glycopyrrolate) Inhalation Solution Now Available in the U.S. for the Treatment of COPD
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Sunovion Submits New Drug Application to the FDA for Apomorphine Sublingual Film (APL-130277) for the Treatment of OFF Episodes Associated with Parkinson’s Disease
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Sunovion Receives FDA Approval of Supplemental New Drug Application (sNDA) for Use of Latuda® (lurasidone HCl) in the Treatment of Bipolar Depression in Pediatric Patients (10 to 17 Years of Age)
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Sunovion Announces Positive Topline Results from Pivotal Study of Apomorphine Sublingual Film (APL-130277) in Patients with Parkinson’s Disease
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Sunovion Receives FDA Approval for Lonhala™ Magnair™ Inhalation Solution to Treat COPD
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Sunovion to Present Data on Aptiom® (eslicarbazepine acetate) at the American Epilepsy Society (AES) Annual Meeting 2017

