SNYSanofi

Nasdaq sanofi.com


$ 48.54 $ 0.44 (0.92 %)    

Friday, 28-Jun-2024 15:59:46 EDT
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$ 48.52
$ 48.10
$ 48.35 x 249
$ 48.52 x 200
$ 48.06 - $ 48.94
$ 40.90 - $ 53.45
3,048,949
na
60.96B
$ 0.58
$ 10.21
TBD
na
na ($ 0.08)
na
TBD na
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News

OPINIONS

 sanofis-frexalimab-phase-2-data-shows-41-reduction-in-key-biomarker-of-nerve-cell-damage-in-relapsing-ms-high-dose-arm-demonstrates-significant-drop-in-plasma-neurofilament-light-chain-levels-after-48-weeks-supports-potential-as-high-efficacy-disease-modifying-treatment-phase-3-studies-underway

Frexalimab new phase 2 data showed reduction of key biomarker of nerve cell damage in relapsing MSFrexalimab high-dose arm obse...

Core News & Articles

- Reuters

 first-inhaled-copd-therapy-in-over-2-decades---fda-approves-verona-pharmas-first-commercial-product

The FDA has approved Verona Pharma's Ohtuvayre (ensifentrine) as maintenance treatment of chronic obstructive pulmonary dis...

Core News & Articles

Vigil Neuroscience, Inc. (NASDAQ:VIGL), a clinical-stage biotechnology company committed to harnessing the power of microglia f...

Core News & Articles

The trial showed a greater proportion of those receiving weight-tiered higher dose Dupixent experienced significant improvement...

 sanofi-looks-to-sell-20b-icy-hot-division-likely-bidders-include-advent-pai-partners-blackstone-cvc

Sanofi wants $20 billion for its consumer health division, attracting interest from major firms like Advent and PAI Partners.

 tuesday-sanofi-announced-riliprubart-one-year-follow-up-from-phase-2-study-showed-efficacy-and-safety-and-rapid-and-durable-reduction-of-key-biomarkers-including-those-associated-with-classical-complement-pathway-and-nerve-cell-damage

https://www.sanofi.com/en/media-room/press-releases/2024/2024-06-25-20-30-00-2904145

 sanofi-seeks-bids-for-20b-consumer-arm-by-mid-july-advent-pai-among-top-suitors-blackstone-cdr-cvc-and-tpg-also-interested

- Bloomberg Citing Sources

 sanofi-to-present-altuviiios-long-term-efficacy-and-fitusirans-prophylaxis-potential-at-isth

ISTH: Sanofi advances leadership in hemophilia with new data for ALTUVIIIO and fitusiran Seven oral presentations across the...

 industry-groups-back-gsks-effort-to-halt-70000-lawsuits-associated-with-heartburn-drug-zantac-caused-cancer

GSK, supported by major industry groups, seeks to stop 70,000 Zantac lawsuits in Delaware, arguing a recent court ruling threat...

Core News & Articles

SAR443579/IPH6101, ANKET® platform lead asset, is a first-in-class NKp46/CD16-based NK cell engager targeting CD123 from a jo...

Core News & Articles

-Reuters

 sanofi-highlights-data-from-blood-cancer-drug-sarclisa-in-new-diagnosed-multiple-myeloma-patients

Sanofi's phase 3 IMROZ study shows Sarclisa with VRd significantly improves progression-free survival in newly diagnosed, t...

 zantac-heart-burn-continues-for-gsk-as-us-court-ruling-allows-thousands-of-zantac-lawsuits-to-move-forward

GSK shares fell as the Delaware State Court allowed over 70,000 lawsuits regarding the discontinued heartburn drug Zantac (rani...

 dhl-supply-chain-expands-pharma-logistics-operations-in-france---dhl-group

https://group.dhl.com/en/media-relations/press-releases/2024/dhl-supply-chain-expands-pharma-logistics-operations-in-france.html

 fda-extends-review-deadline-for-regeneronsanofis-dupixent-for-smokers-lungs-disease

The FDA extends the target action date for reviewing Dupixent as an add-on treatment for uncontrolled COPD to September 27, 202...

Core News & Articles

Dupixent recommended for EU approval by the CHMP to treat patients with COPD Recommendation for adults with uncontrolled COP...