Genentech
Genentech articles from Informachine.Genentech rejects Roche’s $43.7-billion takeover offer as too low
13 Aug 2008
Biotechnology giant Genentech Inc today rejected a $43.7-billion takeover bid from its majority shareholder, Roche Holding AG, as too low, while saying it would be open to a higher proposal.
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Latest articles on Genentech from Informachine
Genentech and Roche Present New Data Across Pharmaceuticals and Diagnostics From Its Growing Alzheimer’s Disease Portfolio at CTAD 2026
10 Nov 2026
Updated Phase Ib/IIa Brainshuttle™ AD study data for trontinemab demonstrating rapid amyloid removal dynamics and changes in key biomarkers
Genentech’s Divarasib Demonstrated Best-In-Class Efficacy, Advancing the Standard of Care in Previously Treated KRAS G12C-Mutated Lung Cancer
25 Oct 2026
Divarasib monotherapy demonstrated superior efficacy over first-generation KRAS G12C inhibitors, lowering the risk of disease progression or death by 42% and the overall risk of death by 44%, in the Phase III Krascendo 1 study
Genentech Presents Interim Phase III Data Showing Sefaxersen Significantly Reduced Proteinuria in People With IgA Nephropathy (IgAN)
23 Oct 2026
Sefaxersen achieved a statistically significant 43.1% reduction in proteinuria, a key indicator of kidney damage, relative to placebo at 37 weeks with consistent treatment effects across all prespecified patient subgroups
Genentech Presents New Pivotal Trial Data Across Broad Neuroimmunology Portfolio at MSToronto2026
21 Oct 2026
Genentech will present new Phase III data across its neuroimmunology portfolio at MSToronto2026, including research on fenebrutinib, an investigational BTK inhibitor, and Ocrevus for people living wit
Genentech to Present Pivotal Data at ESMO 2026, Showcasing Advances Across Its Lung and Breast Cancer Late-Stage Portfolio
19 Oct 2026
Phase III Krascendo 1 results demonstrated divarasib’s superiority over first-generation KRAS G12C inhibitors in previously treated advanced G12C-mutated non-small cell lung cancer
FDA Approves First-In-Class IL-6R Inhibitor as The First And Only At-Home Subcutaneous Treatment Option For Thyroid Eye Disease (TED)
16 Oct 2026
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FDA Approves Genentech’s Enspryng, a First-in-Class IL-6R Inhibitor, as the First and Only At-Home Subcutaneous Treatment Option for Thyroid Eye Disease (TED)
16 Oct 2026
FDA approval based on Phase III SatraGO-1 and -2 studies, with SatraGO-2 demonstrating a significant reduction in eye bulging (proptosis) and improvement in diplopia (double vision), with a favorable
Genentech Presents New Phase III One-Year Data for Vamikibart in Uveitic Macular Edema (UME), a Serious Cause of Vision Loss
11 Oct 2026
In the MEERKAT and SANDCAT studies, vamikibart demonstrated sustained improvements in vision and reductions in macular thickness in patients with UME at 52 weeks.
FDA Approves Genentech’s Tecentriq in Combination With a Fluoropyrimidine and Oxaliplatin for The Adjuvant Treatment of a Certain Type of Stage III Colon Cancer
09 Oct 2026
FDA approval is based on results from the landmark Phase III ATOMIC study, published in The New England Journal of Medicine, which showed Tecentriq plus chemotherapy reduced the risk of disease recurr
Genentech and Breastcancer.Org Say It’s “About Damn Time” We Talk About What Happens When Initial Breast Cancer Treatment Ends
01 Oct 2026
More than 225,000 women in the U.S. are expected to be diagnosed with hormone receptor HR+, HER2- breast cancer this year, the most common form of the disease, representing approximately 70% of cases
