Chugai Pharma USA
Business Services · New Jersey, United States · 201-500 Employees
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Overview
Headquarters
300 Connell Dr Ste 3100, Berkeley Height...Phone Number
(908) 516-1350Website
www.chugai-pharm.comRevenue
$22 MillionIndustry
About Chugai Pharma USA
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Chugai Pharma USA News & Media
Chugai's HEMLIBRA® Receives Regulatory Approval from U.S. FDA for Hemophilia A Without Inhibitors
TOKYO--(BUSINESS WIRE)--#biotech--Chugai Pharmaceutical Co., Ltd. (TOKYO:4519) announced today that the U.S. Food and Drug Administration (FDA) has approved HEMLIBRA® (US generic name: emicizumab-kxwh), a treatment for hemophilia A created by Chugai, for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and children, ages newborn and older, with hemophilia A without factor VIII inhibitors, administered once weekly, every two weeks, or every four weeks. The FDAResults of Global Phase III Study with Chugai's HEMLIBRA® for Hemophilia A Without Inhibitors Published in the New England Journal of Medicine
TOKYO--(BUSINESS WIRE)--#biotech--Chugai Pharmaceutical Co., Ltd. (TOKYO:4519) today announced that results of the HAVEN 3 study (NCT02847637), the global phase III study evaluating hemophilia A treatment, HEMLIBRA® (generic name: emicizumab [genetical recombination]), were published in the 30 August 2018 issue of the New England Journal of Medicine (NEJM).Article: https://www.nejm.org/doi/full/10.1056/NEJMoa1803550Quick video summary by NEJM: https://www.nejm.org/do/10.1056/NEJMdo005333/full/ TChugai's Anti-IL-31 Receptor A Humanized Monoclonal Antibody "nemolizumab," Long Term Data from Global Phase II Study Published in Journal of Allergy and Clinical Immunology Online
TOKYO--(BUSINESS WIRE)--#atopicdermatitis--Long term data from global phase 2 study for Chugai's nemolizumab was published in Journal of Allergy and Clinical Immunology Online.Chugai's HEMLIBRA® Receives Breakthrough Therapy Designation from U.S. FDA for Hemophilia A Without Factor VIII Inhibitors
TOKYO--(BUSINESS WIRE)--#biotech--Chugai Pharmaceutical Co., Ltd. (TOKYO:4519) announced today that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation for its anti-coagulation factor IXa/X humanized bispecific monoclonal antibody / coagulation factor VIII substitute, “HEMLIBRA®” [US generic name: emicizumab-kxwh] for people with hemophilia A without factor VIII inhibitors. Development and distribution of the drug in the US is conducted by Genentech, a member
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Frequently Asked Questions Regarding Chugai Pharma USA
Chugai Pharma USA, Inc. (CPUSA) is a subsidiary of Chugai Pharmaceutical Co., Ltd., located in Berkeley Heights, NJ. The company specializes in planning and executing global and U.S. clinical programs for innovative new drug candidates developed by Chugai. CPUSA emphasizes partnerships in healthcare solutions and is committed to integrity and socia... Read More