Press Releases
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- Jul 14, 2016Eisai and Arena Pharmaceuticals Announce Regulatory Approval of VENESPRI® (lorcaserin HCl) in MexicoFirst Country in Latin America to Approve lorcaserin
Eisai Inc. and Arena Pharmaceuticals, Inc. (NASDAQ: ARNA) today announced that the Federal Commission for the Protection Against Sanitary Risk (COFEPRIS) has granted regulatory approval of the...
- Jun 29, 2016Eisai Highlights its Strong Pipeline and Innovative Approach to R&D at Company's U.S. Scientific Day-- "Ricchi" philosophy focuses on hardest-to-treat medical conditions, including dementia
Eisai Inc., the U.S. pharmaceutical subsidiary of Eisai Co., Ltd., today held a Scientific Day to present its approach to global R&D and introduce the company's robust neurology and oncology...
- Jun 22, 2016
Eisai Inc., the U.S. pharmaceutical subsidiary of Eisai Co., Ltd., announced today that it will host a Scientific Day on June 29, 2016 from 9:00 a.m. EDT to 12:45 p.m. EDT in New York City, and...
- Jun 15, 2016New FDA-Approved Formulation Indicated as Adjunctive Therapy for the Treatment of Partial-Onset Seizures and Primary Generalized Tonic-Clonic Seizures
Eisai Inc. announced today the availability of FYCOMPA® (perampanel) Oral Suspension, a new bioequivalent interchangeable alternative to the FYCOMPA tablet for patients who have difficulty...
- Jun 14, 2016Two-day forum conducted to identify innovative resources that may help patients with rare, severe form of epilepsy
Eisai Inc. and the Lennox-Gastaut Syndrome (LGS) Foundation held a hackathon event, called #HackLGS, bringing together LGS caregivers, technology developers, students and creative specialists on...
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Jun 2, 2016Combination treatment recently approved by FDA for Patients with Advanced Renal Cell Carcinoma Following Prior Anti-angiogenic Therapy
Eisai Inc., the U.S. pharmaceutical subsidiary of Eisai Co., Ltd., and Novartis Pharmaceuticals Corporation, an affiliate of Basel, Switzerland-based Novartis AG, have entered into an agreement to...
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May 24, 2016- Abstracts include sub-analysis from second pivotal trial of Halaven® to show overall survival advantage, which supported January FDA approval in advanced liposarcoma
Eisai Inc. announced today presentations of new analyses of studies supporting U.S. Food and Drug Administration (FDA) approvals at the 2016 American Society of Clinical Oncology (ASCO) Annual...
- May 24, 2016
Eisai Inc., the U.S. pharmaceutical subsidiary of Eisai Co., Ltd., today announced the immediate appointment of Maria Garrigan, as Vice President, Global Regulatory Strategy for the Oncology...
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May 13, 2016- Near-tripling in progression-free survival demonstrated by LENVIMA and everolimus when compared with a standard of care advances treatment paradigm in this category
Eisai Inc. announced today that the U.S. Food and Drug Administration (FDA) approved LENVIMA® (lenvatinib), the company's multiple receptor tyrosine kinase inhibitor, in combination with...
- May 2, 2016New Formulation Expands Treatment Options for Epilepsy Patients with POS and PGTC Seizures
Eisai Inc. today announced that the U.S. Food and Drug Administration (FDA) has approved FYCOMPA® (perampanel) CIII Oral Suspension as adjunctive therapy for the treatment of partial-onset...
