Kyowa Kirin Taiwan Co., Ltd.
Company name
Group Parent Subsidiary Customer Supplier Alliance Bank Shareholder
BioWa, Inc.
Group company Parent Subsidiary Customer Supplier Alliance Bank, lending and credit Investment, equity and shareholders
Group
Kyowa Kirin USA Holdings, Inc.
Group company Parent Subsidiary Customer Supplier Alliance Bank, lending and credit Investment, equity and shareholders
Group

15 entries
DateDescription
2020 Poteligeo® launched in Europe for the treatment for mycosis fungoides (MF) and Sézary syndrome (SS).
2020 Crysvita® approved in the US for the treatment of tumor-induced osteomalacia (TIO).
2021 New Vision toward 2030 designed to realize the creation and delivery of life-changing value.
2021 Agreement reached with Amgen to jointly develop and commercialize KHK4083, a Kyowa Kirin-discovered anti-OX40 fully human monoclonal antibody.
2021 Declared support for the recommendations of the Task Force on Climate-Related Financial Disclosures (TCFD).
2022 Global DE&I Statement adopted with 40% of global leaders to be female by 2030.
2022 An automated injection device "G-Lasta® Subcutaneous Injection 3.6 mg BodyPod" launched in Japan for the long-acting G-CSF preparation, G-Lasta®.
2022 Q-TOWER, the new biopharmaceutical analysis facility completed at Takasaki Plant, Kyowa Kirin's major biopharmaceutical manufacturing site.
2023 PHOZEVEL® approved in Japan for the treatment of Hyperphosphatemia in chronic kidney disease patients.
2023 Kyowa Kirin announced the acquisition of UK company Orchard Therapeutics with strength in hematopoietic stem cell gene therapy.
2024 Lenmeldy™ , an innovative hematopoietic stem cell (HSC) gene therapy, approved and launched in the United States.
2024 A new biologics manufacturing plant decided to be established in North Carolina, the United States.
2024 A global strategic collaboration signed to develop and commercialize menin inhibitor ziftomenib in acute leukemias with Kura Oncology.
2025 Completion of the HB7 Building, a new biopharmaceutical DS (Drug Substance) manufacturing facility at the Takasaki Plant, to strengthen global manufacturing capacity and talent development.
2025 FDA approval and U.S. launch of KOMZIFTI™ (ziftomenib) for adult AML (Acute Myeloid Leukemia).
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2026-09-21 18:05 (Model: ggml-org/gpt-oss-20b )
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