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Qingdao Primedicine Pharmaceutical Co. Ltd and Primary Peptides Inc. Announce...
QINGDAO, China & VANCOUVER, British Columbia Qingdao Primedicine Pharmaceutical Co. Ltd., a leading biotech company in China, and Primary Peptides Inc, a privately held biotech company in...
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Rising Pharmaceuticals to Support Phase 2 Clinical Trial of Chloroquine...
EAST BRUNSWICK N.J. Rising Pharma Holdings Inc., the pharmaceutical company now operating as Rising Pharmaceuticals, today announced the support of a Phase 2 clinical trial designed to determine the...
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Genetron Health Announces Strategic Collaboration with DARUI on GENETRON S5...
BEIJING Genetron Holdings Limited (“Genetron Health”), a China-based precision oncology company that covers full-cycle cancer care, announced that it has joined forces with DARUI. The partnership...
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PROTECT III試験、高リスクPCI前のImpella留置がベイルアウトPCIと比較して死亡率が低いことを示す
米マサチューセッツ州ダンバース （ビジネスワイヤ） —...
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ENHERTU® Granted Orphan Drug Designation in the U.S. for Gastric Cancer
TOKYO & BASKING RIDGE, N.J. Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) and AstraZeneca’s ENHERTU® (fam-trastuzumab deruxtecan-nxki) has been granted Orphan Drug Designation...
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Daiichi Sankyo Initiates Clinical Trial with 5th DXd ADC, DS-6157, in...
TOKYO & MUNICH & BASKING RIDGE, N.J. & NASHVILLE, Tenn. Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) and Sarah Cannon Research Institute (Sarah Cannon) announced today...
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U.S. FDA Approves Takeda’s ALUNBRIG® (brigatinib) as a First-Line Treatment...
CAMBRIDGE, Mass. & OSAKA, Japan Takeda Pharmaceutical Company Limited (TSE:4502/NYSE:TAK) today announced that the U.S. Food and Drug Administration (FDA) approved ALUNBRIG (brigatinib) for...
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美国FDA核准武田ALUNBRIG® (brigatinib)用作一种罕见严重类型肺癌患者的一线治疗选择
马萨诸塞州剑桥和日本大阪 (美国商业资讯)–武田药品工业株式会社(Takeda Pharmaceutical Company Limited) (TSE:4502/NYSE:TAK)今天宣布，美国食品药品管理局(FDA)核准ALUNBRIG...
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希少な重篤肺がんと診断された患者に対するファーストライン治療としての武田薬品のALUNBRIG®（ブリガチニブ）を米国FDAが承認
米マサチューセッツ州ケンブリッジ & 大阪 （ビジネスワイヤ） —...
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Terns Pharmaceuticals to Present at Jefferies Virtual Healthcare Conference
FOSTER CITY, Calif. & SHANGHAI Terns Pharmaceuticals, Inc., a global biopharmaceutical company focused on discovering and developing innovative therapies to treat liver disease and cancer, today...
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Takara Bio Announces the Completion of a New GMP Facility for Manufacturing...
MOUNTAIN VIEW, Calif. Takara Bio USA, Inc. (TBUSA) announced that its parent company, Takara Bio Inc., has completed the construction of a new facility, the Center for Gene and Cell Therapy...
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Qurient Announces U.S. FDA Clearance of IND Application for Q702, a Novel...
SEONGNAM-SI, Korea Qurient Co. Ltd. (KRX: 115180), a clinical stage biotech company in Korea, today announced that the U.S. Food and Drug Administration (FDA) has cleared its investigational new...
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EdiGene and Immunochina Announce Research and Development Collaboration to...
BEIJING, China & CAMBRIDGE, Mass. EdiGene, Inc., which develops genome editing technologies to accelerate drug discovery and develop novel therapeutics for a broad range of diseases, and...
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Vaxxas Announces That MSD Exercises Option to Apply Novel Immune System...
BRISBANE, Australia Vaxxas, a biotechnology company commercializing a novel vaccination platform, today announced that MSD, the tradename of Merck & Co., Inc., Kenilworth, NJ USA, has exercised...
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New data show first-line triplet regimen of pembrolizumab, Herzuma®...
INCHEON, South Korea Data presented today as part of the ASCO20 Virtual Scientific Program show that a first-line triplet regimen comprising of pembrolizumab, Herzuma® (biosimilar trastuzumab) and...
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Alteogen Presents the First-in-Human Data on ALT-P7, a HER2-targeting...
DAEJEON, South Korea Alteogen Inc. (KOSDAQ:196170) has today presented at ASCO results from the First-in-Human (FIH), phase 1 study of ALT-P7, a HER2-targeting antibody-drug conjugate (ADC), in...
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Takeda Announces Compelling Data from the Phase 2 Trial of Pevonedistat Plus...
CAMBRIDGE, Mass. & OSAKA, Japan Takeda Pharmaceutical Company Limited (TSE:4502/NYSE:TAK) today announced the results of the Phase 2 Pevonedistat-2001 trial will be presented during oral...
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ENHERTU® Achieved a Tumor Response Rate of 45.3% in Patients with HER2...
TOKYO & BASKING RIDGE, N.J. & MUNICH Results from the phase 2 DESTINY-CRC01 trial of Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) and AstraZeneca’s ENHERTU® (fam-trastuzumab...
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Daiichi Sankyo Announces Clinical Research Collaboration to Evaluate DS-1062...
TOKYO & MUNICH & BASKING RIDGE, N.J. Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) announced that it has entered into a clinical trial collaboration agreement with a subsidiary...
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ENHERTU® Demonstrated Meaningful Clinical Activity in Patients with HER2...
TOKYO & BASKING RIDGE, N.J. & MUNICH Results from the ongoing phase 2 DESTINY-Lung01 trial showed Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) and AstraZeneca’s ENHERTU®...
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