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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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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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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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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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ENHERTU® Significantly Improved Tumor Response Rate and Overall Survival in...

  TOKYO & BASKING RIDGE, N.J. & MUNICH Detailed results from the positive pivotal randomized, controlled phase 2 DESTINY-Gastric01 trial showed Daiichi Sankyo Company, Limited (hereafter,...

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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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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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Fibralign Announces Strategic Partnership With Terumo

  UNION CITY, Calif. Fibralign Corp., a Stanford spin-out developer of therapeutic biomedical devices, has announced today that it has executed a long term distributor agreement with Terumo...

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武田发布Pevonedistat联合阿扎胞苷治疗较高危MDS患者2期试验的有力数据

  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,...

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武田薬品、高リスクMDS患者でpevonedistatとアザシチジンの併用療法を検討する第2相試験の有力なデータを発表

  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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Noxopharm Reports Veyonda’s Potential in Late-Stage Cancer at ASCO 2020

  SYDNEY At the 2020 American Society of Clinical Oncology (ASCO) Virtual Annual Meeting, Noxopharm, a clinical-stage Australian oncology drug development company, has reported two sets of clinical...

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Genetron Health Receives FDA Emergency Use Authorization for SARS-CoV-2 RNA...

  BEIJING Genetron Holdings Limited (“Genetron Health”), a China-based precision oncology company that covers full-cycle cancer care, announced that its independently developed detection kit for the...

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