
The drugmaker said efficacy and safety data didn't support further development of the drug, amlitelimab, for atopic dermatitis.
Sanofi, a healthcare company, is engaged in the research, development, manufacture, and marketing of therapeutic solutions in the United States, Europe, and internationally. The company is headquartered in Paris, France.
| Revenue (TTM) | $47.35B |
| Gross Profit (TTM) | $34.26B |
| EBITDA | $12.83B |
| Operating Margin | 20.00% |
| Return on Equity | 6.58% |
| Return on Assets | 4.67% |
| Revenue/Share (TTM) | $19.52 |
| Book Value | $34.54 |
| Price-to-Book | 1.27 |
| Price-to-Sales (TTM) | 1.98 |
| EV/Revenue | 2.272 |
| EV/EBITDA | 12.62 |
| Quarterly Earnings Growth (YoY) | -11.70% |
| Quarterly Revenue Growth (YoY) | 6.00% |
| Shares Outstanding | $2.39B |
| Float | $2.17B |
| % Insiders | 0.00% |
| % Institutions | 8.86% |
Volatility is currently contracting

The drugmaker said efficacy and safety data didn't support further development of the drug, amlitelimab, for atopic dermatitis.

Sanofi today announced discontinuation of clinical development of amlitelimab, an OX40-ligand monoclonal antibody, in moderate-to-severe atopic dermatitis.

Sanofi evolves its Executive Committee to support its next strategic chapter Paris, July 21, 2026. Sanofi today announced an evolution of its Executive Committee, bringing together a focused leadership team across its businesses, scientific organization and key global functions as the company continues to deliver on its priorities and prepares its next strategic chapter.

PARIS & LONDON--(BUSINESS WIRE)-- #DrugDiscovery--Aqemia, the drug invention company combining generative AI and quantum-inspired physics to invent small molecule drugs, today announced the expansion of its multi-year research collaboration with the global pharmaceutical company, Sanofi. The expansion is marked by the nomination of a new therapeutic target and an additional payment. The collaboration, first announced in December 2023, makes Aqemia eligible to receive up to a total of $140 million in upfront and.

Sanofi's subcutaneous Sarclisa Escena approved in the US as first anticancer treatment administered via on-body injector

The U.S. Food and Drug Administration said on Friday it has approved Sanofi's blood cancer drug, Sarclisa, which can be given under the skin through a wearable injector, offering multiple myeloma patients a less burdensome alternative to intravenous infusions.

The European Commission said on Wednesday it would seek feedback on commitments offered by French pharmaceutical company Sanofi to address concerns that it may have breached competition rules in a flu vaccine marketing campaign.

Sanofi's phase III Baby-COMET study meets all goals for Nexviazyme in infantile-onset Pompe disease, paving the way for a planned U.S. filing in H2 2026.

Availability of the aide-mémoire for Q2 2026 results Paris, France – July 1, 2026. Sanofi announced today the availability of the aide-mémoire for Q2 2026 results on the "Investors" page of sanofi.com: Second quarter 2026 results Prepared each quarter, this document is intended to support financial modelling of the quarterly results.

The European Commission opened on Friday an investigation into whether French drug giant Sanofi breached EU competition rules in a flu vaccine marketing campaign.
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