Key statistics
On Thursday, Roche Holding AG (RHHVF:QXI) closed at 285.14, 22.31% above the 52 week low of 233.12 set on May 06, 2024.
52-week range
Short selling activityProvided by S&P Global Market Intelligence
Open | 281.13 |
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High | 286.19 |
Low | 279.75 |
Bid | -- |
Offer | -- |
Previous close | 279.58 |
Average volume | 8.24k |
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Shares outstanding | 809.25m |
Free float | 731.58m |
P/E (TTM) | 18.84 |
Market cap | 203.29bn CHF |
EPS (TTM) | 13.23 CHF |
Annual div (ADY) | 10.86 USD |
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Annual div yield (ADY) | 3.81% |
Div ex-date | Mar 14 2024 |
Div pay-date | Mar 18 2024 |
Data delayed at least 15 minutes, as of Nov 21 2024 20:54 GMT.
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- Roche to present new and encouraging long-term follow-up data across broad haematology portfolio at ASH 2024
- Roche presents new data at CTAD, demonstrating its growing momentum in diagnostics for Alzheimer’s disease
- New England Journal of Medicine publishes landmark phase III results for Roche’s Itovebi, showing more than doubling of progression-free survival in certain type of HR-positive advanced breast cancer
- [Ad hoc announcement pursuant to Art. 53 LR] Roche’s strong sales growth of 9% (CER) continues in the third quarter of 2024; Group sales increase 6% in the first nine months
- [Ad hoc-Mitteilung gemäss Art. 53 KR] Starkes Verkaufswachstum der Roche-Gruppe von 9% (CER) auch im dritten Quartal 2024; Konzernverkäufe steigen in den ersten neun Monaten um 6%
- Roche’s Vabysmo improved vision in underrepresented populations with diabetic macular edema (DME) in a first-of-its-kind study
- Majority of children with spinal muscular atrophy (SMA) treated with Roche’s Evrysdi are able to sit, stand and walk independently, two-year data demonstrate
- FDA approves Roche’s Itovebi, a targeted treatment for advanced hormone receptor-positive, HER2-negative breast cancer with a PIK3CA mutation
- Roche obtains CE certification for the first companion diagnostic to identify patients with gastric and gastroesophageal junction cancer eligible for targeted treatment with VYLOY
- Positive phase III results for Roche’s Gazyva/Gazyvaro show superiority to standard therapy alone in people with lupus nephritis
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