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Last updated about 7 hours ago

[Ad hoc announcement pursuant to Art. 53 LR] Roche reports strong 2025 results with 7% sales growth

about 7 hours ago

Group sales grew by 7%1 at constant exchange rates (CER; 2% in...

[Ad hoc announcement pursuant to Art. 53 LR] Roche announces positive Phase II results for its dual GLP-1/GIP receptor agonist CT-388 in people living with obesity

2 days ago

A once-weekly subcutaneous injection of CT-388 achieved a statistically significant placebo-adjusted weight...

FDA approves Roche’s Lunsumio VELO™ for subcutaneous use in relapsed or refractory follicular lymphoma

about 1 month ago

Lunsumio VELO reduces administration time from 2-4 hours to approximately one minuteAvailability...

Roche expands automated mass spectrometry menu with antibiotics drug monitoring CE mark approval offering industry’s broadest in vitro diagnostic menu

about 2 months ago

With this approval, Roche’s automated mass spectrometry platform now offers the industry’s...

Roche’s giredestrant reduced risk of invasive disease recurrence or death by 30% in ER-positive early-stage breast cancer

about 2 months ago

Giredestrant is the only oral SERD to show superior invasive disease-free survival...

European Commission approves Roche’s Gazyva/Gazyvaro for adults with active lupus nephritis

about 2 months ago

Approval based on phase II NOBILITY and phase III REGENCY studies showing...

Roche presents Lunsumio data showing potential across earlier treatment lines in indolent and aggressive lymphomas

about 2 months ago

Lunsumio in combination with lenalidomide may offer an effective treatment in relapsed...

Roche’s Columvi combination shows sustained survival benefit at three-year follow up of pivotal phase III STARGLO study

about 2 months ago

Overall survival was twice as long for people treated with Columvi in...

Roche receives FDA clearance with CLIA waiver and CE Mark for its first point-of-care test for diagnosing Bordetella infections, including whooping cough (pertussis)

about 2 months ago

The point-of-care test delivers PCR-accurate results in just 15 minutes, enabling healthcare...

European Commission approves Roche’s Lunsumio subcutaneous for relapsed or refractory follicular lymphoma

2 months ago

Lunsumio provides high rates of deep and long-lasting responses in third-line and...

[Ad hoc announcement pursuant to Art. 53 LR] Roche’s giredestrant becomes the first oral SERD to show superior invasive disease-free survival in early breast cancer

2 months ago

At interim analysis, giredestrant demonstrated a statistically significant and clinically meaningful benefit...