Sanofi (SNYNF) — 6-K Filings
All 6-K filings from Sanofi. Browse 50 Foreign Current Report reports with AI-powered summaries and risk analysis.
6-K Filings (50)
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Sanofi Updates Tolebrutinib Regulatory Submission
— Dec 29, 2025 Risk: low
On December 24, 2025, Sanofi announced an update regarding its tolebrutinib regulatory submission for non-relapsing secondary progressive multiple sclerosis. Th - 6-K Filing — Dec 23, 2025
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Sanofi Agrees to Lower Drug Costs with US Government
— Dec 22, 2025 Risk: medium
On December 19, 2025, Sanofi announced an agreement with the US government to reduce medicine costs. This agreement aims to balance lower prices with continued - 6-K Filing — Dec 15, 2025
- 6-K Filing — Dec 12, 2025
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Sanofi's Dupixent Gets EU Approval as First Targeted Medicine
— Dec 3, 2025 Risk: low
On November 25, 2025, Sanofi announced that its drug Dupixent, developed with Regeneron, received approval in the European Union as the first targeted medicine -
Sanofi's Dupixent Study Meets Endpoints
— Nov 18, 2025 Risk: low
On November 7, 2025, Sanofi announced that the pivotal study for Dupixent, developed with Regeneron, met all primary and secondary endpoints. This filing is a F - 6-K Filing — Nov 3, 2025
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Sanofi's efdoralprin alfa shows positive results
— Oct 31, 2025 Risk: low
On October 22, 2025, Sanofi announced positive results for its efdoralprin alfa drug. The drug met all primary and key secondary endpoints in a study for alpha- -
Sanofi Prices $3 Billion Bond Issuance
— Oct 28, 2025 Risk: low
On October 28, 2025, Sanofi announced the successful pricing of a USD 3 billion bond issuance. This filing is a Form 6-K report, indicating it's a report of a f -
Sanofi Files 6-K with Mid-Year Financial Updates
— Oct 27, 2025 Risk: low
Sanofi filed a 6-K on October 27, 2025, presenting unaudited condensed half-year consolidated financial statements as of June 30, 2025. These statements should -
Sanofi Files 6-K, Updates EU Rezurock Review
— Oct 24, 2025 Risk: low
On October 17, 2025, Sanofi announced an update regarding the regulatory review of Rezurock for chronic graft-vs-host disease (cGVHD) in the EU. The company als -
Sanofi Files 6-K Report for October 2025
— Oct 24, 2025 Risk: low
On October 24, 2025, Sanofi filed a Form 6-K, reporting its activities for the month of October 2025. This filing includes a press release, Exhibit 99.1, which -
Sanofi's AlphaMedixTM Drug Meets Phase 2 Efficacy Endpoints
— Oct 15, 2025 Risk: low
On October 8, 2025, Sanofi announced that its AlphaMedixTM (212Pb-DOTAMTATE) drug successfully met all primary efficacy endpoints in a Phase 2 study. This devel -
Sanofi Drug SAR446268 Gets FDA Fast Track Nod
— Sep 26, 2025 Risk: low
On September 23, 2025, Sanofi announced that its investigational drug, SAR446268, received U.S. Food and Drug Administration (FDA) Fast Track designation for th -
Sanofi's Dupixent Gets EU Green Light for Urticaria
— Sep 22, 2025 Risk: low
On September 22, 2025, Sanofi announced that its drug Dupixent, developed with Regeneron, received a positive opinion from the European Medicines Agency's Commi -
Sanofi's Tzield approved in China; Q3 sales rise 3.1%
— Sep 17, 2025 Risk: low
On September 10, 2025, Sanofi announced that its drug Tzield received approval in China, marking it as the first disease-modifying therapy for adults with stage -
Sanofi's amlitelimab succeeds in Phase 3 atopic dermatitis study
— Sep 4, 2025 Risk: low
On September 4, 2025, Sanofi announced that its drug amlitelimab successfully met all primary and key secondary endpoints in the COAST 1 Phase 3 study for treat -
Sanofi's Wayrilz Approved in US for Immune Thrombocytopenia
— Sep 3, 2025 Risk: low
On August 29, 2025, Sanofi announced that its drug Wayrilz (tirabrutinib) received US approval as the first BTK inhibitor for immune thrombocytopenia (ITP). Thi -
Sanofi's Rilzabrutinib Gets EU Orphan Designation
— Aug 29, 2025 Risk: low
On August 14, 2025, Sanofi announced that its drug rilzabrutinib received Orphan Drug Designation from the European Union for the treatment of IgG4-related dise -
Sanofi Completes Vigil Neuroscience Acquisition
— Aug 7, 2025 Risk: low
On August 6, 2025, Sanofi announced the completion of its acquisition of Vigil Neuroscience, Inc. The filing incorporates a press release detailing this signifi -
Sanofi's Sarclisa Gets EU Approval for Multiple Myeloma
— Jul 31, 2025 Risk: low
On July 25, 2025, Sanofi announced that its drug Sarclisa received EU approval for treating transplant-eligible newly diagnosed multiple myeloma. This marks a s -
Sanofi Files 6-K Report for July 2025
— Jul 31, 2025 Risk: low
On July 31, 2025, Sanofi filed a Form 6-K, reporting on events for the month of July 2025. The filing incorporates by reference a press release issued by the co -
Sanofi's SAR446597 Gets FDA Fast Track for Geographic Atrophy
— Jul 22, 2025 Risk: low
On July 16, 2025, Sanofi announced that its investigational drug, SAR446597, received Fast Track designation from the U.S. Food and Drug Administration (FDA) fo -
Sanofi Files 6-K Report
— Jul 18, 2025 Risk: low
On July 18, 2025, Sanofi filed a Form 6-K with the SEC, reporting information as of the same date. The filing indicates Sanofi's principal executive offices are -
Sanofi's Riliprubart Gets US Orphan Drug Nod
— Jul 2, 2025 Risk: low
On June 25, 2025, Sanofi announced that its investigational antibody, riliprubart, received Orphan Drug Designation from the U.S. Food and Drug Administration ( -
Sanofi's Dupixent Outperforms Xolair in CRS Study
— Jun 24, 2025 Risk: low
On June 15, 2025, Sanofi announced that its drug Dupixent showed superiority over Xolair (omalizumab) in treating chronic rhinosinusitis with nasal polyps (CRSw -
Sanofi Prices €1.5 Billion Bond Issue
— Jun 18, 2025 Risk: low
On June 17, 2025, Sanofi announced the successful pricing of a €1.5 billion bond issuance. This financial move is part of the company's ongoing funding strategy -
Sanofi Ramps Up Beyfortus Shipments Ahead of RSV Season
— Jun 17, 2025 Risk: low
On June 9, 2025, Sanofi announced the acceleration of global shipping for its Beyfortus (nirsevimab-afm) product. This initiative aims to ensure healthcare prov -
Sanofi's Rilzabrutinib gets US Orphan Drug status for sickle cell
— Jun 6, 2025 Risk: low
On June 3, 2025, Sanofi announced that its drug Rilzabrutinib received Orphan Drug Designation from the U.S. Food and Drug Administration (FDA) for the treatmen -
Sanofi and Blueprint Medicines Announce Collaboration
— Jun 2, 2025 Risk: low
On June 2, 2025, Sanofi announced a joint press release with Blueprint Medicines Corporation. This filing incorporates the press release as Exhibit 99.1, detail -
Sanofi Completes DR-0201 Acquisition, Updates on Beyfortus
— May 30, 2025 Risk: low
On May 27, 2025, Sanofi announced the completion of its acquisition of DR-0201. Additionally, on May 29, 2025, Sanofi provided an update on its product Beyfortu -
Sanofi to Acquire Vigil Neuroscience for $1.4B
— May 22, 2025 Risk: medium
On May 22, 2025, Sanofi announced its intention to acquire Vigil Neuroscience, Inc. for an aggregate value of $1.4 billion. This acquisition aims to bolster San -
Sanofi Files 6-K on April 30th Annual Meeting
— May 5, 2025 Risk: low
Sanofi filed a Form 6-K on May 5, 2025, reporting on its Annual General Meeting held on April 30, 2025. The filing includes a press release from April 30, 2025, -
Sanofi Closes Opella Deal, Creates Consumer Health Leader
— Apr 30, 2025 Risk: low
On April 30, 2025, Sanofi announced the closing of its transaction with CD&R for Opella, its global consumer healthcare business. This strategic move aims to es -
Sanofi Files 6-K Report for April 2025
— Apr 24, 2025 Risk: low
On April 24, 2025, Sanofi filed a Form 6-K, reporting on events for the month of April 2025. This filing includes a press release, attached as Exhibit 99.1, whi -
Sanofi's Dupixent Approved for Chronic Spontaneous Urticaria in US
— Apr 22, 2025 Risk: low
On April 18, 2025, Sanofi announced that its drug Dupixent received US FDA approval as a new targeted therapy for chronic spontaneous urticaria (CSU). This mark -
Sanofi Respiratory Pipeline Advances with New Asthma Data, COPD Studies Planned
— Apr 16, 2025 Risk: low
On April 15, 2025, Sanofi announced advancements in its respiratory pipeline, presenting new data for asthma treatments and outlining plans for new clinical stu -
Sanofi's Tolebrutinib Shows MS Disability Benefit in Phase 3
— Apr 10, 2025 Risk: low
Sanofi announced on April 8, 2025, that Phase 3 data for its drug tolebrutinib, published in the New England Journal of Medicine (NEJM), demonstrated a benefit -
Sanofi's Rilzabrutinib Gets Orphan Drug Status for Rare Diseases
— Apr 4, 2025 Risk: low
On April 3, 2025, Sanofi announced that its investigational drug, Rilzabrutinib, received Orphan Drug Designation from the U.S. Food and Drug Administration (FD -
Sanofi's Dupixent Approved in Japan for COPD
— Apr 2, 2025 Risk: low
On March 28, 2025, Sanofi announced that Dupixent received approval in Japan as the first biologic medicine for patients suffering from Chronic Obstructive Pulm -
Sanofi's Tolebrutinib Gets FDA Priority Review for MS
— Mar 26, 2025 Risk: medium
On March 25, 2025, Sanofi announced that the U.S. Food and Drug Administration (FDA) has accepted for priority review its supplemental New Drug Application (sND -
Sanofi to Acquire Dren Bio to Boost Immunology Pipeline
— Mar 20, 2025 Risk: low
On March 20, 2025, Sanofi announced its intention to acquire Dren Bio, Inc. for an undisclosed amount. This acquisition aims to bolster Sanofi's immunology pipe -
Sanofi's Dupixent Shows Promise in Bullous Pemphigoid Trial
— Mar 10, 2025 Risk: low
On March 8, 2025, Sanofi announced positive pivotal data for Dupixent in treating bullous pemphigoid, presented at the American Academy of Dermatology (AAD) ann -
Sanofi Prices EUR 1.5 Billion Bond Issue
— Mar 6, 2025 Risk: low
On March 5, 2025, Sanofi announced the successful pricing of a EUR 1.5 billion bond issue. This filing is a Form 6-K report for the month of March 2025, indicat -
Sanofi Presents New Duvakitug Data at ECCO 2025
— Feb 28, 2025 Risk: low
On February 22, 2025, Sanofi announced new data for its drug duvakitug at the ECCO 2025 conference. The data presented reinforce the drug's potential as a best- -
Sanofi's Dupixent Gets FDA Priority Review for Bullous Pemphigoid
— Feb 20, 2025 Risk: low
On February 18, 2025, Sanofi announced that the U.S. Food and Drug Administration (FDA) accepted for priority review a supplemental Biologics License Applicatio -
Sanofi ExPEC Vaccine Phase 3 Study Update
— Feb 13, 2025 Risk: low
On February 13, 2025, Sanofi announced an update regarding its Phase 3 clinical study for an extraintestinal pathogenic E. coli (ExPEC) vaccine. The company rep -
Sanofi Files 6-K Reporting Press Release Publication
— Feb 7, 2025 Risk: low
In February 2025, Sanofi filed a Form 6-K to report the publication of a press release, attached as Exhibit 99.1. This filing is for the month of February 2025 -
Sanofi's Sarclisa Gets EU Approval for Multiple Myeloma
— Feb 3, 2025 Risk: low
On January 31, 2025, Sanofi announced that its drug Sarclisa, in combination with standard therapy, became the first anti-CD38 treatment approved in the EU for
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