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0QQ6

Roche (0QQ6)

Roche Holding Ag
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일자시간출처헤드라인심볼기업
2025/03/1715:00UK RegulatoryRoche to share latest scientific advancements from its neuromuscular portfolio at Muscular Dystrophy Association (MDA) 2025 conferenceLSE:0QQ6Roche Holding Ag
2025/03/1215:00UK RegulatoryRoche enters into an exclusive collaboration & licensing agreement with Zealand Pharma to co-develop and co-commercialise petrelintide as a potential foundational therapy for people with overweight and obesityLSE:0QQ6Roche Holding Ag
2025/03/0715:00UK RegulatoryRoche announces launch of Roche Genentech Innovation Center Boston based at Harvard’s Enterprise Research Campus in AllstonLSE:0QQ6Roche Holding Ag
2025/03/0515:00UK RegulatoryFDA accepts supplemental Biologics License Application for Roche’s Gazyva/Gazyvaro for the treatment of lupus nephritisLSE:0QQ6Roche Holding Ag
2025/03/0307:00UK RegulatoryPhase III study shows Xolair may be more effective with fewer side effects than oral immunotherapy for the treatment of food allergiesLSE:0QQ6Roche Holding Ag
2025/02/2822:15UK RegulatoryCHMP recommends EU approval of Roche’s Columvi combination for people with relapsed or refractory diffuse large B-cell lymphomaLSE:0QQ6Roche Holding Ag
2025/02/2103:30UK RegulatoryRoche unveils a new class of next-generation sequencing with its novel sequencing by expansion technologyLSE:0QQ6Roche Holding Ag
2025/02/1301:45UK RegulatoryFDA approves Roche’s Evrysdi tablet as first and only tablet for Spinal Muscular Atrophy (SMA)LSE:0QQ6Roche Holding Ag
2025/02/0717:45UK RegulatoryNew England Journal of Medicine publishes new data for Roche’s Gazyva/Gazyvaro which shows superiority over standard therapy in people with active lupus nephritisLSE:0QQ6Roche Holding Ag
2025/02/0501:45UK RegulatoryFDA approves Roche’s Susvimo as the first and only continuous delivery treatment for the leading cause of diabetes-related blindnessLSE:0QQ6Roche Holding Ag
2025/02/0101:45UK RegulatoryRoche receives FDA approval for the first companion diagnostic to identify patients with HER2-ultralow metastatic breast cancer eligible for ENHERTULSE:0QQ6Roche Holding Ag
2025/01/3015:00UK Regulatory[Ad hoc announcement pursuant to Art. 53 LR] Roche reports strong 2024 results with 7% sales growth; fourth quarter marks third straight quarter of 9% growthLSE:0QQ6Roche Holding Ag
2025/01/3015:00UK Regulatory[Ad-hoc-Mitteilung gemäss Art. 53 KR] Roche erzielt starkes Jahresergebnis für 2024 mit Verkaufswachstum von 7%; drittes Quartal in Folge mit 9% WachstumLSE:0QQ6Roche Holding Ag
2025/01/2915:00UK RegulatoryChange to the Roche Enlarged Corporate Executive CommitteeLSE:0QQ6Roche Holding Ag
2025/01/2815:00UK RegulatoryRoche’s Itovebi demonstrated statistically significant and clinically meaningful overall survival benefit in a certain type of HR-positive advanced breast cancerLSE:0QQ6Roche Holding Ag
2025/01/2715:00UK RegulatoryRoche announces new results from EMBARK demonstrating significant sustained benefits of Elevidys in ambulatory individuals with Duchenne muscular dystrophy (DMD)LSE:0QQ6Roche Holding Ag
2025/01/2215:00UK RegulatoryRoche receives FDA clearance with CLIA waiver for cobas® liat molecular tests to diagnose sexually transmitted infections at the point of careLSE:0QQ6Roche Holding Ag
2025/01/0815:10UK RegulatoryRoche purchases shares in tender offer for Poseida Therapeutics, Inc.LSE:0QQ6Roche Holding Ag
2024/12/1915:00UK RegulatoryRoche’s Phase IIb study of prasinezumab missed primary endpoint, but suggests possible benefit in early-stage Parkinson’s diseaseLSE:0QQ6Roche Holding Ag
2024/12/1815:00UK RegulatoryRoche transforms mass spectrometry diagnostics with launch of cobas® Mass Spec solutionLSE:0QQ6Roche Holding Ag
2024/12/1315:10UK RegulatoryRoche’s Vabysmo prefilled syringe (PFS) approved in the EU for three retinal conditions that can cause blindnessLSE:0QQ6Roche Holding Ag
2024/12/1315:00UK RegulatoryRoche receives CE Mark for new and updated molecular cobas 6800/8800 systems, enhancing laboratory efficiency and testing capabilitiesLSE:0QQ6Roche Holding Ag
2024/12/1015:00UK RegulatoryNew and updated data for Roche's fixed-duration Columvi and Lunsumio at ASH 2024 reinforce their potential to improve outcomes for people with lymphomaLSE:0QQ6Roche Holding Ag
2024/12/1006:30UK RegulatoryRoche commences tender offer for all shares of Poseida Therapeutics, Inc. for $9.00 per share in cash, plus a non-tradeable contingent value right for up to $4.00 per share in cashLSE:0QQ6Roche Holding Ag
2024/12/0902:30UK RegulatoryFive-year results confirm Roche’s Polivy combination therapy as new standard of care for previously untreated aggressive lymphomaLSE:0QQ6Roche Holding Ag
2024/12/0515:00UK RegulatoryFDA accepts supplemental Biologics License Application for Roche’s Columvi combination for people with relapsed or refractory diffuse large B-cell lymphomaLSE:0QQ6Roche Holding Ag
2024/11/2615:10UK RegulatoryRoche enters into a definitive agreement to acquire Poseida Therapeutics, including cell therapy candidates and related platform technologiesLSE:0QQ6Roche Holding Ag
2024/11/2615:00UK RegulatoryRoche reports update on Phase III SKYSCRAPER-01 study resultsLSE:0QQ6Roche Holding Ag
2024/11/0523:15UK RegulatoryRoche to present new and encouraging long-term follow-up data across broad haematology portfolio at ASH 2024LSE:0QQ6Roche Holding Ag
2024/10/3115:15UK RegulatoryRoche presents new data at CTAD, demonstrating its growing momentum in diagnostics for Alzheimer’s diseaseLSE:0QQ6Roche Holding Ag
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