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Roche Holding Aktie News

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WKN:  851311 ISIN:  CH0012032113 US-Symbol:  RHHBF Branche:  Pharmazeutika Land:  Schweiz
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Roche Holding News

06.10.25 - GlobeNewswire
Roche receives CE Mark for AI-based Kidney Klinrisk Algorithm(1) and launches new comprehensive chronic kidney disease (CKD) algorithm panel
Roche, in collaboration with KlinRisk, Inc, has received CE-mark for the first AI-based risk stratification tool for assessment of progressive decline in kidney function. This tool will be ...
03.10.25 - GlobeNewswire
FDA approves Roche’s Tecentriq plus lurbinectedin as first-line maintenance therapy for extensive-stage small cell lung cancer
Combination reduced the risk of disease progression or death by 46% and risk of death by 27% in pivotal phase III IMforte study 1 First and only combination therapy for the first-​line ...
03.10.25 - GlobeNewswire
Change in the Roche Board of Directors
Basel, 3 October 2025 - Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today that Dr. Claudia Süssmuth Dyckerhoff has decided not to stand for re-​election as a member of the ...
01.10.25 - GlobeNewswire
Roche commences tender offer for all shares of 89bio, Inc. for $14.50 per share in cash, plus a non-tradeable contingent value right for up to $6.00 per share in cash
Basel, 1 October 2025 - Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has commenced a tender offer for all of the outstanding shares of common stock of 89bio, ...
30.09.25 - GlobeNewswire
Data show Roche’s sixth-generation Troponin T test offers a new level of accuracy critical for diagnosing heart attacks
Recently granted CE Mark, the novel test delivers improved sensitivity and accuracy for faster and more reliable diagnosis in emergencies. The test helps clinicians quickly identify ...
24.09.25 - GlobeNewswire
Roche presents new data for OCREVUS and fenebrutinib across broad patient populations at ECTRIMS 2025
OCREVUS subcutaneous maintains consistent benefit-​risk profile after two years New late-​breaking data confirms OCREVUS significantly reduces disability progression in adults ...
22.09.25 - GlobeNewswire
Positive phase III results show Roche’s giredestrant significantly improved progression-free survival in ER-positive advanced breast cancer
evERA met its co-​primary endpoints; giredestrant plus everolimus demonstrated significant benefit in ITT and  ESR1 -mutated populations in post-CDK inhibitor setting, compared ...
19.09.25 - GlobeNewswire
CHMP recommends EU approval of Roche’s subcutaneous formulation of Lunsumio for people with relapsed or refractory follicular lymphoma
Lunsumio provides high and long-​lasting response rates, with approximately two-​thirds of patients with a complete response in remission after four years 1 Subcutaneous ...
18.09.25 - GlobeNewswire
Roche enters into a definitive merger agreement to acquire 89bio, and its phase 3 FGF21 analog for the therapy of moderate to severe MASH
89bio’s pegozafermin allows for a potentially best-​in-disease treatment for moderate to severe Metabolic Dysfunction-​Associated Steatohepatitis (MASH), one of the most prevalent ...
05.09.25 - GlobeNewswire
New data for Roche's Vabysmo reinforce its efficacy, safety and durability in neovascular or “wet” age-related macular degeneration (nAMD)
In AVONELLE-​X, the largest long-term extension trial in nAMD, disease control and durability were maintained over 4 years, with nearly 80% of patients on extended dosing by study ...
04.09.25 - GlobeNewswire
Roche receives CE mark for Contivue, its Port Delivery Platform containing Susvimo, for neovascular age-related macular degeneration (nAMD)
Susvimo is under review with the EMA and once approved will be the first continuous delivery treatment for nAMD, affecting 1,7 million in the European Union 1 New seven-​year data ...
30.08.25 - GlobeNewswire
Roche and Alnylam advance zilebesiran into global phase III cardiovascular outcomes trial for people with uncontrolled hypertension
Phase III trial informed by comprehensive KARDIA data set generated through three Phase II studies: KARDIA-1, KARDIA-2 and KARDIA-3 In the Phase II KARDIA-3 study, presented ...
25.08.25 - GlobeNewswire
Roche’s US subsidiary Genentech breaks ground on state-of-the-art manufacturing facility in North Carolina, USA
The $700 million project is part of Roche’s $50 billion investment in US manufacturing, infrastructure and R&D. The facility will create more than 1,900 jobs and support the ...
01.08.25 - GlobeNewswire
Roche’s Susvimo maintains vision over five years with two refills per year in people with neovascular age-related macular degeneration (nAMD)
Susvimo is the only continuous delivery treatment to provide reliable, long-term vision outcomes in nAMD, the leading cause of vision loss in people over the age of 60 With two ...
28.07.25 - GlobeNewswire
Roche presents new insights in Alzheimer’s disease research across its diagnostics and pharmaceutical portfolios at AAIC
Trontinemab’s Phase Ib/IIa Brainshuttle™ AD study continues to show rapid and robust clearance of amyloid plaques, with 91% becoming amyloid PET negative and ARIA-E ...
25.07.25 - GlobeNewswire
Roche provides regulatory update on Elevidys™ gene therapy for Duchenne muscular dystrophy in the EU
EMA’s CHMP issued an opinion not to recommend Elevidys™ (delandistrogene moxeparvovec) for the treatment of ambulatory individuals with Duchenne muscular dystrophy (DMD) ...
24.07.25 - GlobeNewswire
[Ad hoc announcement pursuant to Art. 53 LR] Roche continues strong momentum with 7% growth (CER) in the first half of 2025
Basel, 24 July 2025
24.07.25 - GlobeNewswire
[Ad-hoc-Mitteilung gemäss Art. 53 KR] Roche setzt starkes Wachstum im ersten Halbjahr 2025 fort: Verkäufe steigen um 7% (CER)
Basel, 24. Juli 2025
23.07.25 - GlobeNewswire
Roche receives CE Mark for minimally invasive blood test to help rule out Alzheimer’s disease
Elecsys pTau181 is the first In Vitro Diagnostic Regulation (IVDR) certified test to rule out Alzheimer’s associated amyloid pathology. The minimally invasive, blood-​based test can ...
23.07.25 - GlobeNewswire
European Commission approves Roche’s Itovebi for people with ER-positive, HER2-negative, advanced breast cancer with a PIK3CA mutation
Approval based on INAVO120 data showing the Itovebi™ (inavolisib)-based regimen more than doubled progression-​free survival compared with palbociclib and fulvestrant alone 1 ...

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