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0QQ6

Roche (0QQ6)

Roche Holding Ag
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 Showing the most relevant articles for your search:LSE:0QQ6
DateTimeSourceHeadlineSymbolCompany
09/26/20241:00AMUK RegulatoryPositive phase III results for Roche’s Gazyva/Gazyvaro show superiority to standard therapy alone in people with lupus nephritisLSE:0QQ6Roche Holding Ag
09/24/20241:00AMUK RegulatoryRoche launches the first test to use its breakthrough TAGS technology for high throughput, simultaneous detection of 12 respiratory virusesLSE:0QQ6Roche Holding Ag
09/23/20241:00AMUK RegulatoryWHO endorses dual-stain cytology (CINtec PLUS) testing in its cervical cancer prevention guidelines, advancing patient care and underlining Roche’s role in pioneering cervical cancer solutionsLSE:0QQ6Roche Holding Ag
09/19/20241:00AMUK RegulatoryPositive phase III results show Xofluza significantly reduces the transmission of influenza virusesLSE:0QQ6Roche Holding Ag
09/16/20241:00AMUK RegulatoryFDA approves OCREVUS ZUNOVO™ as the first and only twice-a-year 10-minute subcutaneous injection for people with relapsing and progressive multiple sclerosisLSE:0QQ6Roche Holding Ag
09/13/20241:00AMUK RegulatoryFDA approves Roche’s Tecentriq Hybreza, the first and only subcutaneous anti-PD-(L)1 cancer immunotherapyLSE:0QQ6Roche Holding Ag
09/10/202410:00AMUK RegulatoryRoche eröffnet Pharmaforschungs- und Entwicklungszentrum in Basel, um wissenschaftliche Innovationen zu beschleunigenLSE:0QQ6Roche Holding Ag
09/10/202410:00AMUK RegulatoryRoche opens Pharma Research and Development Center in Basel to accelerate scientific innovationLSE:0QQ6Roche Holding Ag
09/04/20242:00AMUK RegulatoryRoche’s fenebrutinib demonstrated near-complete suppression of disease activity and disability progression for up to 48 weeks in patients with relapsing multiple sclerosisLSE:0QQ6Roche Holding Ag
08/27/20241:00AMUK RegulatoryRoche’s PiaSky approved in the EU as the first monthly subcutaneous treatment for people with PNHLSE:0QQ6Roche Holding Ag
08/20/20248:30AMUK RegulatoryRoche responds to WHO’s declaration of a global health emergency due to the ongoing mpox outbreakLSE:0QQ6Roche Holding Ag
07/30/20241:00AMUK RegulatoryEuropean Commission approves Roche’s Vabysmo for treatment of retinal vein occlusion (RVO)LSE:0QQ6Roche Holding Ag
07/29/20241:00AMUK RegulatoryRoche closes acquisition of LumiraDx’s Point of Care technology to expand access to diagnostic testing in primary careLSE:0QQ6Roche Holding Ag
07/25/20241:00AMUK Regulatory[Ad hoc announcement pursuant to Art. 53 LR] Roche sales increase by 5% (CER) in first half of 2024; strong growth in second quarter – full-year earnings outlook raisedLSE:0QQ6Roche Holding Ag
07/18/20247:20AMUK RegulatoryNew data for Roche’s Susvimo demonstrates sustained efficacy in two serious diabetic eye conditionsLSE:0QQ6Roche Holding Ag
07/17/202411:45AMUK RegulatoryRoche’s Vabysmo showed extended durability, continued efficacy and a consistent safety profile in long-term diabetic macular edema (DME) studyLSE:0QQ6Roche Holding Ag
07/17/20241:00AMUK Regulatory[Ad hoc announcement pursuant to Art. 53 LR] Roche announces positive Phase I results of its oral GLP-1 receptor agonist CT-996 for the treatment of people with obesityLSE:0QQ6Roche Holding Ag
07/09/20241:00AMUK RegulatoryRoche receives CE Mark for its AI-enabled continuous glucose monitoring solution offering critical predictions to people living with diabetesLSE:0QQ6Roche Holding Ag
07/08/202411:45AMUK RegulatoryRoche to reintroduce Susvimo in the US for people with neovascular age-related macular degeneration (nAMD)LSE:0QQ6Roche Holding Ag
07/05/20241:00AMUK RegulatoryFDA approves Roche’s Vabysmo prefilled syringe (PFS) for three leading causes of vision lossLSE:0QQ6Roche Holding Ag
07/04/20241:00AMUK Regulatory[Ad hoc announcement pursuant to Art. 53 LR] Roche provides update on phase II/III SKYSCRAPER-06 study in metastatic non-squamous non-small cell lung cancerLSE:0QQ6Roche Holding Ag
06/28/20247:15AMUK RegulatoryRoche’s Vabysmo gets CHMP recommendation for third indication retinal vein occlusion (RVO)LSE:0QQ6Roche Holding Ag
06/28/20247:00AMUK RegulatoryCHMP recommends EU approval of Roche’s PiaSky for people with PNH, a rare, life-threatening blood conditionLSE:0QQ6Roche Holding Ag
06/27/20241:00AMUK RegulatoryRoche expands access to cervical cancer screening tools with two new WHO prequalification designations, including HPV self-collectionLSE:0QQ6Roche Holding Ag
06/25/20241:00AMUK RegulatoryRoche’s OCREVUS subcutaneous administration approved by European Commission, as first and only twice-a-year injection for relapsing and primary progressive multiple sclerosisLSE:0QQ6Roche Holding Ag
06/24/20241:00AMUK RegulatoryRoche launches new analytical units for cobas® pro integrated solutions delivering greater efficiency and capacity to laboratoriesLSE:0QQ6Roche Holding Ag
06/20/20241:00AMUK RegulatoryRoche launches new highly-sensitive test to more easily diagnose patients who may have B-cell lymphomaLSE:0QQ6Roche Holding Ag
06/15/202410:00AMUK RegulatoryRoche’s Phase III STARGLO study demonstrates Columvi significantly extends survival in people with relapsed or refractory diffuse large B-cell lymphomaLSE:0QQ6Roche Holding Ag
06/10/20241:05AMUK RegulatoryRoche four-in-one molecular test for SARS-CoV-2, Influenza A/B viruses and RSV receives U.S. FDA Emergency Use AuthorizationLSE:0QQ6Roche Holding Ag
06/10/20241:00AMUK RegulatoryEuropean Commission approves Roche’s Alecensa as the first and only targeted adjuvant treatment for people with ALK-positive early-stage lung cancerLSE:0QQ6Roche Holding Ag
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