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ROCHE HOLDING LTD S/ADR - RHHBY STOCK NEWS

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Roche Holdings Ltd. S/ADR (RHHBY) is a leading biotechnology company with a global presence in the field of in-vitro diagnostics. Roche focuses on scientific excellence to develop medicines and diagnostics for improving and saving lives. The company's pivotal role in personalized healthcare is reflected in its commitment to transforming healthcare delivery. Roche's innovative approach encompasses the discovery and development of cutting-edge treatments, including the first CD20xCD3 bispecific antibody, Columvi® (glofitamab), for relapsed or refractory diffuse large B-cell lymphoma (DLBCL). The company's recently FDA-cleared whole-slide imaging system, VENTANA DP 200, signifies Roche's dedication to revolutionizing pathology workflows through digitalization and artificial intelligence-based tools, ensuring pathologists can provide accurate and timely diagnoses. Roche's extensive portfolio and pipeline of haematology medicines demonstrate its unwavering commitment to advancing treatment options for patients worldwide.

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Roche receives CE Mark approval for VENTANA HER2 (4B5) Rabbit Monoclonal Primary Antibody RxDx to identify metastatic breast cancer patients with low HER2 expression, potentially benefiting from ENHERTU treatment. The test aids in assessing HER2-low status, expanding treatment options for patients.
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Roche's cobas Malaria test receives FDA approval for screening U.S. blood donors, offering a sensitive solution to detect Plasmodium parasites and improve blood safety.
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Roche shareholders approve all Board proposals, re-elect Severin Schwan as Chairman, and increase dividend for the 37th consecutive year. The company reports strong performance in Pharmaceuticals and Diagnostics Divisions with a focus on oncology, immunology, neurology, and new areas like obesity.
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Roche introduces navify Analytics and Monitoring solutions for laboratories and point of care services, aiming to enhance operational efficiency and financial outcomes. The suite offers actionable insights to improve productivity, reduce costs, and optimize test turnaround times.
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Roche and Alnylam's Phase II KARDIA-2 study of zilebesiran for hypertension met its primary endpoint, showing significant blood pressure reductions. The study demonstrated promising safety and tolerability, supporting potential twice-yearly dosing. The companies have initiated the Phase II KARDIA-3 study. Hypertension is a global health crisis with high mortality rates, affecting one in three adults worldwide.
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Roche's Xolair shows promising results in treating food allergies in NIH-sponsored Phase III study, leading to FDA approval for expanded use in children and adults. The study reveals increased tolerance to peanuts, tree nuts, egg, milk, and wheat in multi-food allergic patients as young as 1 year old, reducing the risk of severe allergic reactions.
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Genentech, a member of the Roche Group, has received FDA approval for Xolair to reduce allergic reactions in patients with IgE-mediated food allergy. The approval is based on positive data from the NIH-sponsored Phase III OUtMATCH study, showing improved tolerance to food allergens in patients as young as 1 year old.
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Roche (RHHBY) partners with PathAI to develop AI digital pathology algorithms for companion diagnostics, aiming to advance precision medicine. The collaboration will enhance patient access to targeted treatments by integrating AI-interpretation into pathology labs globally.
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Genentech, a member of the Roche Group, announced new 72-week data from two global Phase III studies evaluating Vabysmo in macular edema due to branch and central retinal vein occlusion. The data showed that nearly 60% of people receiving Vabysmo were able to extend their treatment intervals to three or four months apart. Patients maintained vision gains and retinal drying for more than one year. Vabysmo is approved in the U.S. and more than 90 countries for people with wet AMD and DME.
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Roche announces positive 72-week data from global Phase III studies evaluating Vabysmo in macular edema due to retinal vein occlusion. Up to 60% of patients were able to extend treatment intervals to three or four months apart. The drug maintained vision gains and retinal drying for more than a year, with well-tolerated safety profiles. Vabysmo is the first and only bispecific antibody approved for the eye, targeting angiopoietin-2 and vascular endothelial growth factor-A. It is approved in the US for RVO and in over 90 countries for nAMD and DME.
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FAQ

What is the current stock price of ROCHE HOLDING S/ADR (RHHBY)?

The current stock price of ROCHE HOLDING S/ADR (RHHBY) is $34.89 as of December 23, 2024.

What is the market cap of ROCHE HOLDING S/ADR (RHHBY)?

The market cap of ROCHE HOLDING S/ADR (RHHBY) is approximately 235.1B.

What is Roche Holdings Ltd. S/ADR (RHHBY) known for?

Roche is a global leader in biotechnology, specializing in in-vitro diagnostics and the development of cutting-edge medicines.

What is the significance of Columvi® (glofitamab) in Roche's portfolio?

Columvi® (glofitamab) is the first CD20xCD3 bispecific antibody that has shown promising results in treating relapsed or refractory diffuse large B-cell lymphoma (DLBCL).

How does Roche contribute to personalized healthcare?

Roche aims to transform healthcare delivery by focusing on scientific excellence, data insights, and partnerships with stakeholders to provide tailored treatment options for patients.

What recent innovation has Roche introduced in digital pathology?

Roche's VENTANA DP 200 whole-slide imaging system, with FDA clearance, allows pathologists to review and interpret digital pathology images efficiently, facilitating remote diagnosis and collaboration.

What is Roche's approach to advancing haematology treatments?

Roche has a robust portfolio and pipeline of haematology medicines, including T-cell engaging bispecific antibodies like Columvi®, to address the diverse needs of patients with blood cancers.

ROCHE HOLDING LTD S/ADR

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RHHBY Stock Data

235.09B
5.12B
0.97%
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