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SNY Overview

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$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
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Intellectia

Loading chart...

High
42.470
Open
42.340
VWAP
42.24
Vol
4.09M
Mkt Cap
101.45B
Low
41.855
Amount
172.55M
EV/EBITDA(TTM)
7.70
Total Shares
2.39B
EV
102.04B
EV/OCF(TTM)
7.49
P/S(TTM)
1.92
Sanofi SA is a France-based healthcare company based in France. The Company focuses on patient needs and engages in the research, development, manufacture, and marketing of therapeutic solutions. Its three operating segments are: Pharmaceuticals, Consumer Healthcare (CHC), and Vaccines. The Pharmaceuticals includes: Immunology, Multiple Sclerosis / Neurology, Oncology, Rare Diseases, Rare Blood Disorders, Cardiovascular, Diabetes, Established Prescription Products. The Vaccines segment comprises, for all geographical territories, the commercial operations of Sanofi Pasteur, together with research, development, and production activities dedicated to vaccines. The CHC segment comprises the commercial operations for Sanofi’s Consumer Healthcare products, together with research, development and production activities dedicated to those products. The Company’s products developed in collaboration or franchise include Dupixent, Aubagio, Lemtrada, Cerezyme, Lumizyme, Jevtana, Fabrazyme.
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Events Timeline

(ET)
2026-06-15
13:00:00
CMS Proposes Permanent Drug Price Negotiation Framework
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link
2026-06-10 (ET)
2026-06-10
16:30:00
US Stocks Drop Sharply Amid Renewed US-Iran Tensions
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2026-06-10
12:10:00
Major U.S. Averages Decline Amid Escalating Geopolitical Tensions
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News

NASDAQ.COM
9.0
06-19NASDAQ.COM
PinnedJapan Approves Sarclisa Subcutaneous Injection for Multiple Myeloma
  • New Drug Approval: French pharmaceutical giant Sanofi announced that its Sarclisa (isatuximab) subcutaneous formulation has been approved in Japan for multiple myeloma patients, marking a significant advancement in the oncology sector.
  • Expanded Indications: The approval for Sarclisa SC includes its use in combination with approved standard treatment regimens, such as with pomalidomide and dexamethasone for relapsed or refractory multiple myeloma, and with bortezomib, lenalidomide, and dexamethasone for newly diagnosed patients, showcasing its broad clinical application potential.
  • Clinical Research Support: This approval is based on results from the IRAKLIA phase 3 study, which demonstrated non-inferiority of Sarclisa SC compared to intravenous administration in treating relapsed or refractory multiple myeloma, further enhancing its market competitiveness.
  • Innovative Delivery Method: Sanofi's CirCLIQ on-body injector (OBI) is currently under review in Japan, and if approved, Sarclisa SC will become the first anticancer treatment administered via an OBI, significantly improving patient convenience and adherence to treatment.
NASDAQ.COM
7.5
06-19NASDAQ.COM
Denali Sells Rare Pediatric Disease Priority Review Voucher for $195 Million
  • Significant Transaction: Denali Therapeutics announced the sale of its Rare Pediatric Disease Priority Review Voucher (PRV) for $195 million, providing a substantial non-dilutive capital infusion that significantly strengthens its financial position.
  • Product Background: The PRV was granted following the FDA's accelerated approval of Avlayah (tividenofusp alfa-eknm) in March 2026 for treating Hunter syndrome, highlighting the drug's market potential and the company's competitiveness in the rare disease sector.
  • Advancing Clinical Portfolio: The capital infusion will aid Denali in advancing its broad Transport Vehicle-enabled clinical portfolio focused on lysosomal storage disorders and neurodegenerative diseases, further solidifying its position in the biopharmaceutical industry.
  • Collaborations and R&D: Denali collaborates with pharmaceutical giants like Sanofi, Biogen, and Takeda to develop various candidates, and despite the discontinuation of the BIIB122 project with Biogen due to unmet expectations, the company will continue to independently advance other key studies, demonstrating resilience and promising prospects in its R&D efforts.
seekingalpha
9.0
06-13seekingalpha
FDA Approves Expanded Use of Sanofi's Diabetes Therapy Tzield
  • Indication Expansion: The FDA has approved Sanofi's Tzield therapy for expanded use in stage 3 diabetes patients, aiming to delay insulin production decline in children aged 8 to 17, marking a significant broadening of treatment scope.
  • Clinical Trial Support: This approval is backed by data from the PROTECT Phase 3 trial, which demonstrated that patients on Tzield experienced a significant slowdown in C-peptide decline, indicating its effectiveness in delaying diabetes progression.
  • Accelerated Approval Pathway: Tzield's accelerated approval allows it to delay the onset of stage 3 diabetes in stage 2 patients, reflecting the FDA's recognition of the therapy's potential benefits, which could lead to greater market opportunities for Sanofi.
  • Follow-up Research Plans: Sanofi is currently enrolling patients in the BETA-PRESERVE Phase 3 study, aiming to convert the accelerated approval into standard approval, further solidifying its position in the diabetes treatment landscape.
NASDAQ.COM
9.0
06-13NASDAQ.COM
Sanofi's Tzield Receives FDA Accelerated Approval
  • FDA Accelerated Approval: Sanofi's Tzield (teplizumab-mzwv) has received FDA accelerated approval for delaying endogenous insulin production decline in children aged 8 to 17 recently diagnosed with stage 3 type 1 diabetes, marking a significant advancement in diabetes treatment.
  • Clinical Research Support: This approval is based on results from the PROTECT phase 3 study and additional data from a global clinical development program involving over 900 patients, demonstrating Tzield's effectiveness in delaying insulin decline, potentially opening new market opportunities for the company.
  • Adverse Reaction Concerns: Common adverse reactions associated with Tzield include lymphopenia, vomiting, and rash, with serious events such as cytokine release syndrome and viral reactivation risks, which may affect patient willingness to use the drug and market acceptance.
  • Global Regulatory Dynamics: Beyond the U.S., Tzield has also been approved in several countries including the UK, EU, and China, indicating its potential in global markets, while facing ongoing regulatory reviews in other jurisdictions that could impact future sales growth.
stocktwits
9.5
06-12stocktwits
Dianthus Therapeutics Receives Strong Buy Rating Following Positive Trial Results
  • Clinical Trial Success: Dianthus Therapeutics reported that 75% of patients in its trial for claseprubart, aimed at chronic inflammatory demyelinating polyneuropathy (CIDP), showed significant improvement, exceeding the company's expectation of 50%, thereby enhancing its competitive position in the market.
  • Positive Market Reaction: Following the announcement of favorable clinical data, Dianthus's stock surged 8% on Friday, marking its best performance since March, indicating strong investor confidence in its future potential.
  • Analyst Rating Maintained: Investment bank Raymond James reaffirmed its 'Strong Buy' rating on Dianthus, keeping the price target at $125 per share, reflecting a positive market outlook, especially in comparison to competing drugs from Sanofi.
  • Future Guidance: Dianthus expects to provide guidance on the timing of Part B top-line results by the end of 2026, further increasing investor interest in its research progress, particularly in the treatment of CIDP and other neurological disorders.
NASDAQ.COM
8.5
06-12NASDAQ.COM
Biotech Sector Sees Surge in FDA and Global Approvals
  • FDA Approval Boosts Innovation: Guardant Health (GH) secured FDA approval for its Guardant360 CDx liquid biopsy test as a companion diagnostic for Boehringer Ingelheim's HERNEXEOS, highlighting the growing importance of liquid biopsy in advanced cancer treatment, which is expected to drive GH's market share growth.
  • Therapy Expansion: Eli Lilly (LLY) received FDA approval for an every-eight-week maintenance dose of EBGLYSS, with Q1 2026 sales surging 141% to $145 million, reflecting strong demand in its immunology portfolio and further solidifying the company's market position.
  • China Market Breakthrough: Vor Bio (VOR) announced that Telitacicept received approval from China's NMPA, becoming the only approved therapy for Sjögren's disease in the country, supported by positive Phase 3 trial data, which is expected to significantly improve patient quality of life and expand market reach.
  • EU Approval for New Therapy: Sanofi (SNY) secured European Commission approval for Sarclisa in newly diagnosed multiple myeloma patients, based on Phase 3 IRAKLIA trial results, which is expected to enhance Sarclisa's application range and strengthen the company's competitiveness in blood cancer treatment.
Wall Street analysts forecast SNY stock price to rise
5 Analyst Rating
Wall Street analysts forecast SNY stock price to rise
2 Buy
3 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
57.00
Averages
79.36
High
119.07
Current: 0.000
sliders
Low
57.00
Averages
79.36
High
119.07
Deutsche Bank
Buy
to
Buy
downgrade
AI Analysis
2026-06-15
New
Reason
Deutsche Bank
Price Target
AI Analysis
2026-06-15
New
downgrade
Buy
to
Buy
Reason
Deutsche Bank lowered the firm's price target on Sanofi to EUR 95 from EUR 100 and keeps a Buy rating on the shares.
Morgan Stanley
Overweight -> Equal Weight
downgrade
$55 -> $52
2026-05-01
Reason
Morgan Stanley
Price Target
$55 -> $52
2026-05-01
downgrade
Overweight -> Equal Weight
Reason
Morgan Stanley downgraded Sanofi to Equal Weight from Overweight with a price target of $52, down from $55. Q1 results support upside to 2026 numbers and scope for a Q2 guidance raise, but \"the equity story remains catalyst-light\" with key pipeline readouts now in 2027, the analyst tells investors. The analyst added that \"cheap valuation alone may not close the discount.\"
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for SNY
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Valuation Metrics

The current forward P/E ratio for Sanofi SA (SNY.O) is 8.48, compared to its 5-year average forward P/E of 9.82. For a more detailed relative valuation and DCF analysis to assess Sanofi SA's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PE
9.82
Current PE
8.48
Overvalued PE
13.50
Undervalued PE
6.15

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average EV/EBITDA
9.23
Current EV/EBITDA
9.99
Overvalued EV/EBITDA
10.26
Undervalued EV/EBITDA
8.19

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PS
2.52
Current PS
2.04
Overvalued PS
2.76
Undervalued PS
2.28

Financials

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Whales Holding SNY

E
Epoch Investment Partners, Inc.
Holding
SNY
+26.17%
3M Return
L
Lansdowne Partners Limited
Holding
SNY
+25.07%
3M Return
B
Bg Fund Management Luxembourg S.A.
Holding
SNY
+23.36%
3M Return
O
Optiver US LLC
Holding
SNY
+23.29%
3M Return
B
BBK Gestion SGIIC SA
Holding
SNY
+20.00%
3M Return
S
Schroder Investment Management North America Inc.
Holding
SNY
+19.78%
3M Return

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Frequently Asked Questions

What is Sanofi SA (SNY) stock price today?

The current price of SNY is 42.38 USD — it has decreased -0.28

What is Sanofi SA (SNY)'s business?

Sanofi SA is a France-based healthcare company based in France. The Company focuses on patient needs and engages in the research, development, manufacture, and marketing of therapeutic solutions. Its three operating segments are: Pharmaceuticals, Consumer Healthcare (CHC), and Vaccines. The Pharmaceuticals includes: Immunology, Multiple Sclerosis / Neurology, Oncology, Rare Diseases, Rare Blood Disorders, Cardiovascular, Diabetes, Established Prescription Products. The Vaccines segment comprises, for all geographical territories, the commercial operations of Sanofi Pasteur, together with research, development, and production activities dedicated to vaccines. The CHC segment comprises the commercial operations for Sanofi’s Consumer Healthcare products, together with research, development and production activities dedicated to those products. The Company’s products developed in collaboration or franchise include Dupixent, Aubagio, Lemtrada, Cerezyme, Lumizyme, Jevtana, Fabrazyme.

What is the price predicton of SNY Stock?

Wall Street analysts forecast SNY stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for SNY is79.36 USD with a low forecast of 57.00 USD and a high forecast of 119.07 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Sanofi SA (SNY)'s revenue for the last quarter?

Sanofi SA revenue for the last quarter amounts to NaN USD, decreased

What is Sanofi SA (SNY)'s earnings per share (EPS) for the last quarter?

Sanofi SA. EPS for the last quarter amounts to USD, decreased

How many employees does Sanofi SA (SNY). have?

Sanofi SA (SNY) has 76493 emplpoyees as of June 20 2026.

What is Sanofi SA (SNY) market cap?

Today SNY has the market capitalization of 101.45B USD.