Welcome to our dedicated page for Roche Hldg news (Ticker: RHHBY), a resource for investors and traders seeking the latest updates and insights on Roche Hldg stock.
Roche Holding Ltd/ADR (RHHBY) is linked to a stream of news that reflects the company’s activities in biotechnology, pharmaceuticals and diagnostics. Recent announcements from Roche and its U.S. affiliate Genentech highlight regulatory approvals, late‑stage clinical trial results, new diagnostic platforms and agreements related to access and manufacturing.
Investors and healthcare observers following RHHBY news will see updates on oncology and haematology programmes, such as the U.S. Food and Drug Administration’s accelerated approval of Lunsumio VELO, a subcutaneous CD20xCD3 bispecific antibody for relapsed or refractory follicular lymphoma after at least two prior lines of systemic therapy. News also covers Phase III data for the investigational oral SERD giredestrant in ER‑positive early‑stage breast cancer, as well as new data on Lunsumio combinations and long‑term outcomes in lymphomas presented at major scientific meetings.
On the diagnostics side, Roche has reported the U.S. launch of next‑generation cobas 6800/8800 systems and software upgrades, CE Mark approval for its cobas Mass Spec solution reagent pack for antibiotics drug monitoring, and CE Mark for the cobas BV/CV assay for bacterial vaginosis and candida vaginitis. These stories illustrate how the company is expanding its in‑vitro diagnostic menu and enhancing laboratory efficiency.
Additional news items include European Commission approval of Gazyva/Gazyvaro for lupus nephritis and Genentech’s agreement with the U.S. government addressing prescription drug costs and direct‑to‑patient programmes. For users of this page, the RHHBY news feed offers a central place to review such regulatory milestones, clinical trial readouts, product launches and policy‑related developments associated with Roche and the Roche Group.
Roche announced that data for OCREVUS (ocrelizumab) and ENSPRYNG (satralizumab) will be presented at the 37th ECTRIMS Congress on October 13-15, 2021. Data shows OCREVUS provides sustained disability reduction for up to 8 years in primary progressive multiple sclerosis (PPMS) and 7.5 years in relapsing MS (RMS). Additionally, long-term safety analyses demonstrate a favorable benefit-risk profile for OCREVUS. ENSPRYNG shows sustained efficacy and safety over four years in neuromyelitis optica spectrum disorder (NMOSD). New studies exploring disease activity in treatment-naïve patients will also be highlighted.
Roche has announced positive results from the phase II/III 2066 study of Ronapreve™ (casirivimab and imdevimab) in hospitalized COVID-19 patients. The trial met its primary endpoint, demonstrating a significant reduction in viral load among seronegative patients not requiring supplemental oxygen (p=0.0172). The study complements prior findings from the UK's RECOVERY trial, showing numeric improvements across clinical endpoints. Despite these advancements, Ronapreve is not yet authorized for hospitalized COVID-19 patients. The compound is currently available in over 40 countries.
Roche presented new data at the World Muscle Society Congress on its neurological treatments, highlighting the efficacy of Evrysdi in treating spinal muscular atrophy (SMA) in pre-symptomatic babies. The RAINBOWFISH study showed that 80% of infants treated for 12 months achieved independent mobility, and all maintained swallowing ability. Evrysdi is now approved in 58 countries. Additionally, interim results on the investigational gene therapy SRP-9001 for Duchenne muscular dystrophy (DMD) showed lasting motor improvements, supporting further clinical studies.
Roche has launched three new PCR test panels for detecting respiratory pathogens, including influenza and RSV, from a single patient sample. This innovative approach utilizes syndromic testing to provide clinicians with actionable insights more quickly than traditional methods. The flexible testing option aims to optimize patient care by reducing unnecessary diagnostics while enabling targeted therapies. These tests can be integrated with Roche's existing COVID-19 testing solutions on the cobas® 6800/8800 Systems, enhancing operational efficiency amidst the ongoing need for respiratory disease management.
Roche presented new data at the ESMO Congress, highlighting Tecentriq's efficacy in treating early-stage lung cancer. The IMpower010 study showed a 34% reduction in disease recurrence or death among patients with Stage II-IIIA non-small cell lung cancer (NSCLC) expressing PD-L1≥1%. The FDA granted Tecentriq Priority Review as an adjuvant treatment, with a decision due by December 1, 2021. This groundbreaking data could significantly impact the treatment landscape for lung cancer and potentially boost Roche's market performance.
Roche announced the European Medicines Agency's CHMP recommendation for Gavreto (pralsetinib) as a monotherapy for adults with RET fusion-positive advanced non-small cell lung cancer (NSCLC). This marks a potential milestone, as it would be the first targeted treatment approved for first-line RET fusion-positive NSCLC in Europe. The recommendation is based on positive findings from the phase I/II ARROW study, which demonstrated significant clinical activity including a 79% overall response rate in treatment-naïve patients. A final decision from the European Commission is expected soon.
Roche has launched the Digital Pathology Open Environment, enhancing collaboration among software developers to improve personalized healthcare through advanced image analysis. This platform enables secure data exchange, allowing pathologists to access algorithms from third-party developers alongside Roche’s AI tools for improved diagnostic precision. By leveraging this open environment, Roche aims to foster partnerships and expedite the development of next-generation diagnostic tests, ultimately benefiting cancer patients with more targeted treatments.
Roche has announced its definitive agreement to acquire the TIB Molbiol Group, with the transaction expected to close in the fourth quarter of 2021. This acquisition aims to enhance Roche's molecular diagnostics portfolio, particularly in assays for infectious diseases, including SARS-CoV-2 variants. TIB Molbiol, recognized for its rapid assay development, has over 45 CE-IVD assays and more than 100 research use assays available on Roche’s LightCycler PCR systems. The two companies have collaborated for over 20 years, responding swiftly to biological threats.
Genentech, part of Roche Group, will present new oncology data at the ESMO Congress from September 16-21, 2021. Highlights include Phase II results from the coopERA study on giredestrant for ER-positive, HER2-negative breast cancer, and Phase III data from the IMpower010 study showing Tecentriq improves outcomes in early-stage non-small cell lung cancer (NSCLC). Genomic insights from the CUPISCO study may enhance personalized treatment for Cancer of Unknown Primary. This underscores Genentech’s commitment to advancements in oncology.
NeuExcell Therapeutics and Spark Therapeutics, part of Roche Group (OTCQX: RHHBY), announced a collaboration to develop a gene therapy for Huntington’s Disease (HD) on September 7, 2021. The agreement grants Spark access to NeuExcell's neuro-regenerative gene therapy platform and potential milestone payments up to $190 million plus royalties. The partnership aims to leverage Spark's expertise in gene therapy to accelerate the HD program, addressing the challenges of neurodegenerative conditions.