Chugai's Satralizumab Receives FDA Breakthrough Therapy Designation for Neuromyelitis Optica and Neuromyelitis Optica Spectrum Disorders Dec 19, 2018 03:00AM
Chugai’s Satralizumab Meets Primary Endpoint in Phase III Monotherapy Study in NMOSD Dec 19, 2018 03:00AM
Chugai's HEMLIBRA® Approved in Taiwan for the Treatment of Hemophilia A with Factor VIII Inhibitors Dec 4, 2018 02:00AM
Results Presented from Primary Analysis of the Phase III HAVEN 2 Study with Chugai's HEMLIBRA® for Children with Hemophilia A with Inhibitors at the American Society of Hematology 2018 Dec 3, 2018 08:00PM
Chugai Presents Results from Phase III Study of Satralizumab in NMOSD at ECTRIMS 2018 Oct 14, 2018 11:00PM


Oct 12, 2018 12:30AM Chugai Releases Disease Awareness Anime about Rheumatoid Arthritis in Multiple Languages Emphasizing Importance of Early Detection/Treatment and Care by Specialists
Oct 4, 2018 09:00PM Chugai's HEMLIBRA® Receives Regulatory Approval from U.S. FDA for Hemophilia A Without Inhibitors
Aug 30, 2018 01:00AM Results of Global Phase III Study with Chugai's HEMLIBRA® for Hemophilia A Without Inhibitors Published in the New England Journal of Medicine
Jul 26, 2018 03:00AM Announcement of Business Expansion of Chugai Pharmabody Research Pte. Ltd., Chugai's Research Subsidiary
Jul 26, 2018 02:30AM Chugai Enters into Comprehensive Partnership Agreement with Preferred Networks
May 21, 2018 05:44AM Chugai Presents Results of Two Pivotal Phase lll Studies for its Bispecific Antibody HEMLIBRA® at WFH 2018
Apr 17, 2018 01:00AM Chugai's HEMLIBRA® Receives Breakthrough Therapy Designation from U.S. FDA for Hemophilia A Without Factor VIII Inhibitors
Feb 27, 2018 09:20PM Chugai's HEMLIBRA® Approved by European Commission in Hemophilia A with Inhibitors
Jan 28, 2018 06:30PM Chugai's HEMLIBRA® Gains Positive CHMP Opinion in Hemophilia A with Inhibitors
Dec 21, 2017 01:30AM EU Follows US and Approves Chugai's ALK Inhibitor "Alecensa®" as First Line Therapy for ALK-Positive Non-Small Cell Lung Cancer
Dec 7, 2017 02:45AM Chugai's Emicizumab Every Four Weeks Showed Positive Interim Results in Phase III Study
Nov 20, 2017 03:29AM Chugai's Bispecific Antibody Emicizumab Meets Primary Endpoint in Phase lll Study
Nov 16, 2017 06:30PM Chugai's HEMLIBRA® Receives the World's First Regulatory Approval from FDA for Hemophilia A with Inhibitors
Nov 8, 2017 01:00AM Chugai's ALK Inhibitor "Alecensa®" Approved for the Treatment of First Line Therapy on ALK-Positive Non-Small Cell Lung Cancer in the US
Oct 4, 2017 09:20PM Chugai's Bispecific Antibody "ERY974" Results of Preclinical Study Published in Science Translational Medicine
Aug 24, 2017 01:00AM Chugai's Emicizumab Receives Priority Review Designation by FDA for Hemophilia A with Inhibitors
Jun 5, 2017 07:30PM Data of Chugai's Alecensa® Presented at the American Society of Clinical Oncology on Global Phase III ALEX Study
May 11, 2017 12:51AM Results of the J-ALEX Study for Chugai's Alecensa® are Published in "The Lancet" Online
Apr 10, 2017 03:42AM Chugai's Alecensa® Met Its Primary Endpoint in the ALEX Study
Mar 29, 2017 08:01PM Chugai - A*STAR Joint Development Project for Anti-Dengue Virus Antibody Selected as Grant Recipient by the GHIT Fund
Feb 27, 2017 01:00AM Chugai's ALK Inhibitor "Alecensa®" Approved in Taiwan
Dec 22, 2016 04:27AM Chugai's Bispecific Antibody "Emicizumab" for Hemophilia A Meets Primary Endpoint in Phase lll Study
Oct 5, 2016 01:00AM Chugai's ACTEMRA®/RoACTEMRA® Receives Breakthrough Therapy Designation from US FDA for Giant Cell Arteritis
Oct 4, 2016 01:00AM Chugai's Alecensa® Receives Breakthrough Therapy Designation from FDA for First-Line Treatment of ALK Positive Non-Small Cell Lung Cancer
Jul 27, 2016 10:30PM Chugai's Emicizumab Showed Continued Benefits in Patients with Hemophilia A
Jul 20, 2016 07:30PM Chugai and Galderma Announce Global License Agreement for Nemolizumab (CIM331), Novel Biologic for Skin Diseases
May 25, 2016 10:30PM Chugai's Bispecific Antibody "ACE910/Emicizumab" Phase l Data in Patients with Hemophilia A Published in The New England Journal of Medicine Online
May 18, 2016 09:00PM Chugai to Present Japanese Phase III Results on Alecensa® at ASCO
Mar 5, 2016 12:30PM Chugai Announces Phase II Global Study Results of Nemolizumab (CIM331) in Late-breaking Research Forums at AAD
Feb 10, 2016 04:49AM Chugai's ALK Inhibitor "Alecensa®" Trial Stopped Early for Benefit
Dec 14, 2015 01:34AM Chugai's ALK Inhibitor "Alecensa®" Accelerated Approval in Three Months after Priority Review Designation in the US
Nov 30, 2015 03:00AM Chugai Pharma Marketing Changed Its Corporate Name to Chugai Pharma Europe
Oct 1, 2015 08:10PM Company Profile for Chugai Pharmaceutical Co., Ltd.
Sep 10, 2015 02:00AM Launch of Netupitant-Palonosetron Fixed Combination (Akynzeo®) in the UK by Chugai Pharma UK Ltd.
Sep 9, 2015 01:00AM Chugai's ALK Inhibitor "Alectinib," New Drug Application Submitted for ALK Positive Advanced Non-Small Cell Lung Cancer in the United States
Sep 4, 2015 01:00AM Chugai's Bispecific Antibody "ACE910" for the Treatment of Hemophilia A Designated as a Breakthrough Therapy by the US FDA