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Roche report reveals that misconceptions about hepatitis are driving reluctance to test and failure to treat despite rising deaths
Survey finds fear and misconceptions around hepatitis discourage testing, with more than half of respondents assuming they are not at risk
Phase III study shows Xolair may be more effective with fewer adverse effects for the treatment of food allergies
First-ever head-to-head trial comparing Xolair and oral immunotherapy (OIT)
Roche transforms mass spectrometry diagnostics with launch of cobas Mass Spec solution
Clinical mass spectrometry testing offers sensitivity and specificity, providing clinicians with additional diagnostic insights
Roche receives FDA approval for PATHWAY HER2 (4B5) test
The PATHWAY HER2 (4B5) test helps identify patients with previously treated, unresectable or metastatic HER2-positive biliary tract cancer (BTC) who may be eligible for treatment with ZIIHERA
Roche presents new data highlighting advances in Alzheimer’s diagnostics
Roche’s Elecsys Amyloid Plasma Panel shows high accuracy in ruling out Alzheimer's, offering new hope for early and less invasive diagnostics
Novel diagnostic assay for gastric and gastroesophageal junction cancer receives CE Mark approval
Roche obtains CE certification for VENTANA CLDN18 (43-14A) RxDx Assay to identify patients with gastric and gastroesophageal junction cancer eligible for targeted treatment with VYLOY
FDA approves OCREVUS ZUNOVO subcutaneous injection for people with relapsing and progressive multiple sclerosis
OCREVUS ZUNOVO has the potential to expand treatment options to centers without IV infrastructure or with IV constraints
Roche launches new analytical units for cobas pro integrated solutions
The cobas c 703 and cobas ISE neo analytical units deliver greater efficiency and capacity to laboratories
Roche respiratory test receives FDA Emergency Use Authorization
Roche four-in-one molecular test for SARS-CoV-2, Influenza A/B viruses and RSV receives U.S. FDA Emergency Use Authorization
Roche granted FDA Breakthrough Device Designation
The Roche Diagnostics Tina-quant Lp(a) assay measures lipoprotein (a) in a person’s bloodstream
Roche announces FDA approval of HPV self-collection solution
Expanding access and screening options to help eliminate cervical cancer with one of the first HPV self-collection solutions in the US
Roche granted FDA Breakthrough Device Designation for pTau217 blood test
Supporting earlier Alzheimer's disease diagnosis
Roche receives FDA approval for molecular malaria test
The cobas Malaria test is the first FDA-approved molecular test to screen US blood donors for malaria
Roche launches new diagnostic test for the better understanding of immune response to SARS-CoV-2
The test detects T-cell response, which may play an important role in determining if immune protection has been achieved
Roche launches the VENTANA DP 600 slide scanner for digital pathology, enhancing patient care with precision diagnostics
The VENTANA DP 600 is Roche’s new, high-capacity slide scanner that creates high-resolution, digital images of stained tissue samples that help to diagnose cancer and determine a patient’s treatment
Roche launches comprehensive genomic profiling kit to expand access to personalized cancer research
The AVENIO Tumor Tissue Comprehensive Genomic Profiling Kit is the first jointly-developed product that brings together the expertise and reach of Roche with Foundation Medicine’s pioneering leadership in genomic science
Roche’s VENTANA PD-L1 Assay receives FDA approval as a companion diagnostic to identify lung cancer patients eligible for Tecentriq (atezolizumab)
The VENTANA PD-L1 (SP263) Assay helps determine which non-small cell lung cancer patients may benefit from treatment with Tecentriq immunotherapy based on the results of the Phase III IMpower010 study
Roche announced the launch of three molecular PCR diagnostic test panels to detect and differentiate common respiratory pathogens simultaneously
The three new respiratory test panels on cobas 6800/8800 Systems in CE markets will help identify multiple pathogens with overlapping symptoms in patients
Roche receives FDA approval for first companion diagnostic to identify dMMR solid tumor patients eligible for anti-PD-1 immunotherapy
Using cancer biomarkers, the VENTANA MMR RxDx Panel helps determine which tumor patients may benefit from GSK immunotherapy
FDA grants Breakthrough Therapy Designation for Venclexta in combination with azacitidine
The drug aims to treat patients with myelodysplastic syndromes
Roche’s Actemra/RoActemra receives FDA EUA for the treatment of COVID-19
The authorization enables emergency use of Actemra/RoActemra for the treatment of COVID-19 in hospitalized adult and pediatric patients
Roche obtains CE mark for the SARS-CoV-2 Antigen Self-Test Nasal allowing for rapid self-testing of COVID-19 at home
The test will be widely available to individuals through pharmacies and other locations in accordance with local guidelines and testing strategies
Roche’s cobas SARS-CoV-2 test receives FDA emergency use authorization
First commercial test will enable expedited coronavirus testing to meet urgent medical needs