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AZN

AstraZeneca (AZN)

AstraZeneca PLC
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 검색 관련기사 보기:NASDAQ:AZN
일자시간출처헤드라인심볼기업
2024/09/2320:00Business WireDatopotamab deruxtecan final overall survival results reported in patients with metastatic HR-positive, HER2-low or negative breast cancer in TROPION-Breast01 Phase III trialNASDAQ:AZNAstraZeneca PLC
2024/09/2319:44Edgar (US Regulatory)Form 6-K - Report of foreign issuer [Rules 13a-16 and 15d-16]NASDAQ:AZNAstraZeneca PLC
2024/09/2319:32IH Market NewsApollo Eyes $5 Billion Investment in Intel; TSMC and Samsung Explore UAE Chip Projects, and MoreNASDAQ:AZNAstraZeneca PLC
2024/09/2319:27Edgar (US Regulatory)Form 6-K - Report of foreign issuer [Rules 13a-16 and 15d-16]NASDAQ:AZNAstraZeneca PLC
2024/09/2105:34Business WireFLUMIST approved for self-administration in the USNASDAQ:AZNAstraZeneca PLC
2024/09/1820:00Business WireFASENRA approved in the US for eosinophilic granulomatosis with polyangiitisNASDAQ:AZNAstraZeneca PLC
2024/09/1800:22GlobeNewswire Inc.International companies to host live webcasts at Deutsche Bank’s Depositary Receipts Virtual Investor Conference on September 24th and 25th, 2024NASDAQ:AZNAstraZeneca PLC
2024/09/1620:00Business WireIMFINZI® (durvalumab) plus IMJUDO® (tremelimumab-actl) demonstrated unprecedented overall survival in advanced liver cancer with one in five patients surviving five years in HIMALAYA Phase III trialNASDAQ:AZNAstraZeneca PLC
2024/09/1523:30Business WireIMFINZI® (durvalumab) perioperative regimen reduced the risk of recurrence by 32% and the risk of death by 25% vs. neoadjuvant chemotherapy alone in muscle-invasive bladder cancer in the NIAGARA Phase III trialNASDAQ:AZNAstraZeneca PLC
2024/09/1323:00Business WireENHERTU® (fam-trastuzumab deruxtecan-nxki) showed substantial clinical activity in patients with HER2-positive metastatic breast cancer and brain metastasesNASDAQ:AZNAstraZeneca PLC
2024/09/1023:28PR Newswire (US)SOPHiA GENETICS and AstraZeneca Collaborate to Further Expand Global Access to Liquid Biopsy TestingNASDAQ:AZNAstraZeneca PLC
2024/09/1023:16PR Newswire (US)SOPHiA GENETICS and AstraZeneca Collaborate to Further Expand Global Access to Liquid Biopsy TestingNASDAQ:AZNAstraZeneca PLC
2024/09/1019:02IH Market NewsApple Loses EU Dispute; Google’s $2.7 Billion Fine Upheld; Oracle Shares Surge 9%NASDAQ:AZNAstraZeneca PLC
2024/09/1002:50Business WireDatopotamab deruxtecan showed median overall survival of 14.6 months in patients with advanced nonsquamous non-small cell lung cancer in TROPION-Lung01 Phase III trialNASDAQ:AZNAstraZeneca PLC
2024/09/0901:25Business WireNovel computational pathology-based TROP2 biomarker for datopotamab deruxtecan was predictive of clinical outcomes in patients with non-small cell lung cancer in TROPION-Lung01 Phase III trialNASDAQ:AZNAstraZeneca PLC
2024/09/0519:11IH Market NewsQualcomm Develops Mixed Reality Glasses; Verizon to Boost Dividend, Eyes Acquisition; Samsonite Plans US Dual ListingNASDAQ:AZNAstraZeneca PLC
2024/09/0320:00Business WireAstraZeneca advances ambition to improve standards of care in multiple cancer types at WCLC and ESMO 2024NASDAQ:AZNAstraZeneca PLC
2024/08/2321:20IH Market NewsCruise and Uber Join Forces for Robotaxis, Alibaba Shifts Primary Listing to Hong Kong, Altria Hikes Dividend 4.1%NASDAQ:AZNAstraZeneca PLC
2024/08/1620:00Business WireIMFINZI® (durvalumab) approved in the US for the treatment of resectable non-small cell lung cancer before and after surgeryNASDAQ:AZNAstraZeneca PLC
2024/08/1619:21Edgar (US Regulatory)Form 6-K - Report of foreign issuer [Rules 13a-16 and 15d-16]NASDAQ:AZNAstraZeneca PLC
2024/08/1520:00Business WireIMFINZI® (durvalumab) granted Priority Review and Breakthrough Therapy Designation for patients with limited-stage small cell lung cancer in the USNASDAQ:AZNAstraZeneca PLC
2024/07/3019:26Edgar (US Regulatory)Form 6-K - Report of foreign issuer [Rules 13a-16 and 15d-16]NASDAQ:AZNAstraZeneca PLC
2024/07/3019:00IH Market NewsToyota Reports Another Global Production Decline, Delta Sues CrowdStrike, Meta Launches AI Studio for Custom ChatbotsNASDAQ:AZNAstraZeneca PLC
2024/07/2920:00Business WireFixed-duration CALQUENCE® (acalabrutinib) plus venetoclax, with or without obinutuzumab, significantly improved progression-free survival in 1st-line chronic lymphocytic leukemia in AMPLIFY Phase III trialNASDAQ:AZNAstraZeneca PLC
2024/07/2919:00Edgar (US Regulatory)Form 6-K - Report of foreign issuer [Rules 13a-16 and 15d-16]NASDAQ:AZNAstraZeneca PLC
2024/07/2520:00Business WireAstraZeneca’s H1 and Q2 2024 Financial ResultsNASDAQ:AZNAstraZeneca PLC
2024/07/2519:21IH Market NewsU.S. Index Futures Mixed After Tech Sell-Off, Oil Prices Drop on Weak China Demand and Ceasefire ExpectationsNASDAQ:AZNAstraZeneca PLC
2024/07/2519:19IH Market NewsEarnings Updates: Ford Shares Fall 13% on EPS Miss, Stellantis Down 6%, Viking Therapeutics Up 20%, Unilever Up 5%NASDAQ:AZNAstraZeneca PLC
2024/07/2320:00PR Newswire (Canada)Voydeya est approuvé au Canada à titre de traitement d'appoint au ravulizumab ou à l'éculizumab chez les adultes atteints d'une maladie rare, appelée HPN, qui présentent une anémie hémolytique résiduelle attribuable à une hémolyse extravasculairNASDAQ:AZNAstraZeneca PLC
2024/07/2320:00PR Newswire (Canada)Voydeya approved in Canada as add-on therapy to ravulizumab or eculizumab for adults with the rare disease PNH who have residual hemolytic anemia due to extravascular hemolysisNASDAQ:AZNAstraZeneca PLC
 검색 관련기사 보기:NASDAQ:AZN