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日付概要
1890年 Dr. Shibasaburo Kitasato and Dr. Bering discovered that the serum obtained from an animal infected with diphtheria was effective in the treatment of diphtheria and tetanus; they established serum therapy.
1907年 1907 - Establishment of Kirin Brewery Co., Ltd.
1949年 1949 - Establishment of Kyowa Hakko Kogyo Co., Ltd. as a secondary company of Kyowa Sangyo Co., Ltd, as part of industrial readjustment plans.
1951年 1951 - Introduced production technology of Streptomycin, an anti-tubercular drug, from US pharmaceutical company Merck & Co., Inc. and succeeded in its mass production. Contributed to the wiping out of tuberculosis in Japan (beginning of involvement in pharmaceutical business operations).
1956年 1956 - Success of isolation and commercially mass-production of the anticancer drug, Mitomycin C. Invention of the process of L-glutamic acid production by fermentation (a world first).
1959年 Gerald Edelman and Rodney Porter determined the molecular structure of antibodies.
1963年 1963 - Initiation of full-scale involvement in the pharmaceutical business. Release of Mitomycin C, an anticancer drug, and Spiramycin, an antibiotic drug.
1967年 1967 - Release of 5-FU, an anticancer drug.
1971年 1971 - Release of Leunase, an anticancer drug.
1975年 César Milstein, Georges Köhler and Niels Kaj Jerne established the hybridoma technology, which is a technology for producing monoclonal antibodies.
1976年 Dr. Susumu Tonegawa discovered the genetic principle for the generation of antibody diversity.
1982年 1982 - The Research Institute for Production Development foundation begins full-scale research towards the commercialization of erythropoietin.
1986年 The world's first therapeutic antibody "muromonab" was approved.
1988年 1988 - Supported the establishment in the U.S.A. of the La Jolla Institute for Allergy and Immunology (LIAI).
1990年 1990 - Release of ESPO®, an erythropoietin (EPO) drug.
1990年 Antibody engineering technologies were established.
1991年 1991 - Release of GRAN®, G-CSF drug. Release of Coniel, a remedy for hypertension and angina pectoris.
1997年 1997 - Establishment of fully human antibody production technology.
2003年 2003 - Establishment of BioWa, Inc. in the United States to promote Kyowa Hakko's therapeutic antibody business.
2005年 Japan’s first therapeutic antibody "tocilizumab" was approved.
2007年 2007 - The launch of Kirin Pharma Company, Limited. Release of NESP®, a long-acting erythropoietic stimulating drug. Established COMPLEGENT®, a novel antibody engineering technology, and licensed to BioWa, Inc., its subsidiary. Capital alliance between Kyowa Hakko Group and Kirin Group.
2008年 2008 - Release of REGPARA®, a drug for secondary hyperparathyroidism. Spun off its biochemical business, establishing Kyowa Hakko Bio Co., Ltd. Kyowa Hakko Kirin was formed through the merger of Kyowa Hakko Kogyo and Kirin Pharma.
2009年 2009 - Introduced 'Commitment to Life'.
2011年 2011 - Acquired ProStrakan Group plc.
2012年 2012 - Launch of Poteligeo® in Japan, a Therapeutic Antibody for Adult T-cell Leukemia-Lymphoma (ATL).
2013年 2013 - Launch of NOURIAST® tablets 20 mg in Japan, a novel antiparkinsonian agent.
2014年 2014 - ProStrakan completes acquisition of Archimedes. Launch of Sustained-Duration G-CSF Product G-LASTA® in Japan.
2016年 2016 - Rebranding Western Pharmaceutical Subsidiaries to 'Kyowa Kirin'. Launch of LUMICEF® for Psoriasis Treatment in Japan.
2018年 2018 - Crysvita® approved in the US and Europe for X-linked hypophosphatemia. Poteligeo® approved in the US and Europe for mycosis fungoides and Sézary syndrome.
2019年 2019 - Trade name changed to Kyowa Kirin Co., Ltd. Crysvita® launched in Japan for FGF23-related Hypophosphatemic Rickets and Osteomalacia. Nourianz™ launched in the US for Parkinson's disease.
2020年 2020 - Poteligeo® launched in Europe for mycosis fungoides and Sézary syndrome. Crysvita® approved in the US for tumor-induced osteomalacia.
2021年 2021 - New Vision toward 2030. Agreement with Amgen on KHK4083. Support for TCFD recommendations.
2022年 2022 - Adoption of global DE&I statement. Launch of G-Lasta® Subcutaneous Injection 3.6 mg BodyPod. Completion of Q-TOWER analysis facility.
2022年 More than 100 therapeutic antibodies have been approved in Japan, Europe, and the United States.
2023年 2023 - PHOZEVEL® approved in Japan. Acquisition of Orchard Therapeutics announced.
2024年 2024 - Lenmeldy™ approved and launched in the US. New biologics manufacturing plant planned in North Carolina. Collaboration with Kura Oncology on menin inhibitor ziftomenib.
2025年 2025 - Completion of HB7 Building at Takasaki Plant. FDA approval and US launch of KOMZIFTI™ (ziftomenib) for AML.
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2026-06-18 14:31 (Model: gpt-4.1-nano )
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