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武田薬品、第64回米国血液学会（ASH）年次総会で血液がんおよび他の血液疾患の患者へのコミットメントを示すデータを発表へ
大阪 & 米マサチューセッツ州ケンブリッジ （ビジネスワイヤ） — 武田薬品（TSE:4502/NYSE:TAK）は本日、2022年12月10～13日にニューオーリンズで開催される第64回米国血液学会（ASH）年次総会において、企業スポンサー研究のアブストラクト15件を報告すると発表しました。武田薬品の最新の研究では、血液疾患の患者の長期転帰改善に重点を置いています。...
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BeiGene’s BRUKINSA® (zanubrutinib) Demonstrated Superior Progression-Free...
CAMBRIDGE, Mass. & BASEL, Switzerland & BEIJING BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) a global biotechnology company, today presented the final progression-free survival (PFS)...
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athenahealth Expands its Global Corporate Social Responsibility Program in 2022
WATERTOWN, Mass. athenahealth, Inc., a leading provider of network-enabled software and services for medical groups and health systems nationwide, today announced that its athenaGives corporate...
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知临集团宣布完成交易 2023 年到期的 300 万美元可转换票据
NEW YORK & LONDON & PARIS (美国商业资讯)– 知临集团有限公司（纳斯达克股票代码：APM，巴黎泛欧证券交易所股票代码：APM）（“知临集团”或“知临”），一家致力于满足肿瘤、自身免疫性疾病和传染病领域未被满足的医疗需求的临床阶段生物制药公司，今天宣布已完成交易私募发售本金总额为300万美元...
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Aptorum Group Announces Completion of $3 Million Convertible Note due 2023
NEW YORK & LONDON & PARIS Regulatory News: Aptorum Group Limited (Nasdaq: APM, Euronext Paris: APM) (“Aptorum Group” or “Aptorum”), a clinical stage biopharmaceutical company dedicated to...
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百奥赛图自研双抗获FDA批准进入临床试验
中国北京 (美国商业资讯)- 百奥赛图（北京）医药科技股份有限公司（“百奥赛图”，股票代码02315.HK）宣布其自主研发的全球首创双特异性抗体YH008（PD-1 x CD40）的IND申请获得美国FDA批准。此次IND申报由百奥赛图全资子公司祐和医药完成。...
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Biocytogen Announces FDA Clearance of IND Application for Bispecific Antibody...
BEIJING Biocytogen Pharmaceuticals (Beijing) Co., Ltd. (“Biocytogen”, HKEX: 02315) today announced that the US FDA has approved the Investigational New Drug (IND) application for a phase I study of...
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ENHERTU® Recommended for Approval in the EU by CHMP for Patients with HER2...
TOKYO & MUNICH Daiichi Sankyo (TSE: 4568) and AstraZeneca’s (LSE/STO/Nasdaq: AZN) ENHERTU® (trastuzumab deruxtecan) has been recommended for approval in the European Union (EU) as a monotherapy...
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ENHERTU® Approved in the EU for Patients with Previously Treated HER2...
TOKYO & MUNICH Daiichi Sankyo (TSE: 4568) and AstraZeneca’s (LSE/STO/Nasdaq: AZN) ENHERTU® (trastuzumab deruxtecan) has been approved in the European Union (EU) as a monotherapy for the...
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REGiMMUNE Presented Positive Results of RGI-2001 in the Reduction of Acute...
TAIPEI, Taiwan REGiMMUNE Limited, a clinical-stage biopharmaceutical company developing innovative immunotherapies for immune disorders and cancer, today announced the positive results of their...
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Seagen, Astellas and Merck Announce FDA Acceptance of sBLAs for PADCEV®...
BOTHELL, Wash. & TOKYO & RAHWAY, N.J. Seagen Inc. (Nasdaq: SGEN), Astellas Pharma Inc. (TSE:4503) and Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced...
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バイオサイトジェン、二重特異性抗体YH008のIND申請をFDAが承認したと発表
北京 （ビジネスワイヤ） — バイオサイトジェン・ファーマシューティカルズ（北京）（以下「バイオサイトジェン」、HKEX: 02315）は本日、ファーストインクラスの自社開発PD-1 x...
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InnoCare Announces Approval to Conduct a Phase II Clinical Trial of...
BEIJING InnoCare Pharma (HKEX: 09969; SSE: 688428) announced today that the Company has received approval from the Center for Drug Evaluation (CDE) to conduct a single-arm, open-label, multi-cohort...
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Yescarta® Now Approved in Japan for Initial Treatment of Relapsed/Refractory...
SANTA MONICA, Calif. & TOKYO Kite Pharma, Inc., a Gilead Company, (hereafter, Kite) (NASDAQ: GILD) and Daiichi Sankyo Co., Ltd. (hereafter, Daiichi Sankyo) (TSE: 4568) today jointly announced...
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Elpiscience Announces CDE IND Clearance of ES014, a First in Class...
SHANGHAI & SUZHOU, China & GERMANTOWN, Md. Elpiscience Biopharmaceuticals, Inc. (“Elpiscience”), a clinical-stage biopharmaceutical company focused on developing next-generation...
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LegoChem Biosciences and Amgen Enter into a Multi-Target Research...
DAEJEON, South Korea LegoChem Biosciences, Inc. (‘LCB’) (KOSDAQ:141080) announced on December 23 that it has entered into a research collaboration and license agreement with Amgen, whereby it...
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InnoCare Announces Approval of Tafasitamab in Combination With Lenalidomide...
BEIJING InnoCare Pharma (HKEX: 09969; SSE: 688428) announced today the approval of tafasitamab in combination with lenalidomide for adult patients with relapsed or refractory diffuse large B-cell...
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BeiGene Announces Acceptance of 12th Regulatory Submission in China for PD-1...
CAMBRIDGE, Mass. & BASEL, Switzerland & BEIJING BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235), a global biotechnology company announced that the Center for Drug Evaluation (CDE) of the...
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Legend Biotech Announces Acceptance of Its New Drug Application for...
SOMERSET, N.J. Legend Biotech Corporation (NASDAQ: LEGN) (Legend Biotech), a global biotechnology company developing, manufacturing and commercializing novel therapies to treat life-threatening...
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PharmaEssentia to Present at the 41st Annual J.P. Morgan Healthcare Conference
TAIPEI, Taiwan PharmaEssentia Corporation (TPEx:6446), a global biopharmaceutical innovator leveraging deep expertise and proven scientific principles to deliver new biologics in hematology and...
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