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Chugai Releases Disease Awareness Anime about Rheumatoid Arthritis in Multiple Languages Emphasizing Importance of Early Detection/Treatment and Care by Specialists
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Chugai's HEMLIBRA® Receives Regulatory Approval from U.S. FDA for Hemophilia A Without Inhibitors
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Results of Global Phase III Study with Chugai's HEMLIBRA® for Hemophilia A Without Inhibitors Published in the New England Journal of Medicine
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Announcement of Business Expansion of Chugai Pharmabody Research Pte. Ltd., Chugai's Research Subsidiary
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Chugai Enters into Comprehensive Partnership Agreement with Preferred Networks
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Chugai Presents Results of Two Pivotal Phase lll Studies for its Bispecific Antibody HEMLIBRA® at WFH 2018
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Chugai's HEMLIBRA® Receives Breakthrough Therapy Designation from U.S. FDA for Hemophilia A Without Factor VIII Inhibitors
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Chugai's HEMLIBRA® Approved by European Commission in Hemophilia A with Inhibitors
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Chugai's HEMLIBRA® Gains Positive CHMP Opinion in Hemophilia A with Inhibitors
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EU Follows US and Approves Chugai's ALK Inhibitor "Alecensa®" as First Line Therapy for ALK-Positive Non-Small Cell Lung Cancer
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Chugai's Emicizumab Every Four Weeks Showed Positive Interim Results in Phase III Study
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Chugai's Bispecific Antibody Emicizumab Meets Primary Endpoint in Phase lll Study
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Chugai's HEMLIBRA® Receives the World's First Regulatory Approval from FDA for Hemophilia A with Inhibitors
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Chugai's ALK Inhibitor "Alecensa®" Approved for the Treatment of First Line Therapy on ALK-Positive Non-Small Cell Lung Cancer in the US
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Chugai's Bispecific Antibody "ERY974" Results of Preclinical Study Published in Science Translational Medicine
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Chugai's Emicizumab Receives Priority Review Designation by FDA for Hemophilia A with Inhibitors
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Data of Chugai's Alecensa® Presented at the American Society of Clinical Oncology on Global Phase III ALEX Study
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Results of the J-ALEX Study for Chugai's Alecensa® are Published in "The Lancet" Online
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Chugai's Alecensa® Met Its Primary Endpoint in the ALEX Study
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Chugai - A*STAR Joint Development Project for Anti-Dengue Virus Antibody Selected as Grant Recipient by the GHIT Fund
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Chugai's ALK Inhibitor "Alecensa®" Approved in Taiwan
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Chugai's Bispecific Antibody "Emicizumab" for Hemophilia A Meets Primary Endpoint in Phase lll Study
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Chugai's ACTEMRA®/RoACTEMRA® Receives Breakthrough Therapy Designation from US FDA for Giant Cell Arteritis
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Chugai's Alecensa® Receives Breakthrough Therapy Designation from FDA for First-Line Treatment of ALK Positive Non-Small Cell Lung Cancer
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Chugai's Emicizumab Showed Continued Benefits in Patients with Hemophilia A
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Chugai and Galderma Announce Global License Agreement for Nemolizumab (CIM331), Novel Biologic for Skin Diseases
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Chugai's Bispecific Antibody "ACE910/Emicizumab" Phase l Data in Patients with Hemophilia A Published in The New England Journal of Medicine Online
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Chugai to Present Japanese Phase III Results on Alecensa® at ASCO
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Chugai Announces Phase II Global Study Results of Nemolizumab (CIM331) in Late-breaking Research Forums at AAD
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Chugai's ALK Inhibitor "Alecensa®" Trial Stopped Early for Benefit
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Chugai's ALK Inhibitor "Alecensa®" Accelerated Approval in Three Months after Priority Review Designation in the US
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Chugai Pharma Marketing Changed Its Corporate Name to Chugai Pharma Europe
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Company Profile for Chugai Pharmaceutical Co., Ltd.
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Launch of Netupitant-Palonosetron Fixed Combination (Akynzeo®) in the UK by Chugai Pharma UK Ltd.
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Chugai's ALK Inhibitor "Alectinib," New Drug Application Submitted for ALK Positive Advanced Non-Small Cell Lung Cancer in the United States
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Chugai's Bispecific Antibody "ACE910" for the Treatment of Hemophilia A Designated as a Breakthrough Therapy by the US FDA

