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      • 2022
        • 2022
        • Sanofi provides update on Phase 2 study evaluating amcenestrant in ER+/HER2- advanced or metastatic breast cancer
        • Press Release: Xenpozyme® (olipudase alfa) approved in Japan, first and only approved therapy indicated to treat acid sphingomyelinase deficiency
        • Sanofi announces €300 million collaboration with Blackstone Life Sciences to advance an innovative treatment for multiple myeloma
        • Press Release: Sanofi and Seagen announce collaboration to develop and commercialize multiple novel antibody-drug conjugates
        • Press Release: Sanofi moves forward with EUROAPI listing on Euronext Paris
        • Sanofi recognized by S&P as one of the most sustainability-committed companies
        • Nirsevimab significantly protected infants against RSV disease in Phase 3 trial
        • Late-breaking data at 2022 AAAAI Annual Meeting show Dupixent® (dupilumab) significantly improved signs and symptoms of eosinophilic esophagitis
        • Press release: Late-breaking Phase 3 data at AAD 2022 show Dupixent® (dupilumab) significantly improved signs and symptoms of prurigo nodularis
        • Efanesoctocog alfa met primary and key secondary endpoints in pivotal study in hemophilia A, demonstrating superiority to prior factor prophylaxis treatment
        • Press Release: Sanofi continues on path to industry leadership in Immunology with Dupixent® (dupilumab) as key driver
        • Press Release: Sanofi and IGM Biosciences Announce Collaboration Agreement for Oncology, Immunology and Inflammation Targets
        • Press Release: Availability of the Q1 2022 Memorandum for modelling purposes
        • Press Release: Sanofi unveils new corporate brand and logo – unites the company under one purpose and a single identity
        • Press Release: Sanofi teams up with McLaren Racing to accelerate industrial excellence
        • FDA accepts Dupixent® (dupilumab) for Priority Review in children aged 6 months to 5 years with moderate-to-severe atopic dermatitis
        • Press Release: FDA accepts Dupixent® (dupilumab) for Priority Review in patients aged 12 years and older with eosinophilic esophagitis
        • Olipudase alfa shown to provide sustained improvement across multiple clinical manifestations of ASMD
        • Update on ongoing Dupixent® (dupilumab) chronic spontaneous urticaria Phase 3 program
        • Press Release: EUROAPI listing on Euronext Paris expected on May 6, 2022
        • Press Release: Sanofi continues to deliver strong business EPS growth driven by higher sales and improved margins in Q1
        • Filing of the 2021 U.S. Form 20-F and French “Document d’Enregistrement Universel” containing the Annual Financial Report
        • Exscientia and Sanofi establish strategic research collaboration to develop AI-driven pipeline of precision-engineered medicines
        • Nirsevimab EMA regulatory submission accepted under accelerated assessment for RSV protection in all infants
        • Press Release: Positive Phase 1/2 study results of rilzabrutinib in people with immune thrombocytopenia published in The New England Journal of Medicine
        • Sanofi and Regeneron provide regulatory update on Libtayo® (cemiplimab-rwlc) in advanced cervical cancer
        • Press Release: Sanofi launches first-in-pharma Diversity, Equity & Inclusion Board
        • Press Release: Sanofi successfully priced an inaugural sustainability-linked bond indexed on access to medicines
        • Late-breaking phase 3 data at 2022 AAAAI Annual Meeting show Dupixent® (dupilumab) significantly reduced itch and hives in patients with chronic spontaneous urticaria
        • Availability of the Q4 2021 Memorandum for modelling purposes
        • New preclinical tolebrutinib data demonstrated superior brain penetration and potency
        • Positive Dupixent® (dupilumab) data across five diseases with underlying type 2 inflammation to be presented at 2022 AAAAI Annual Meeting
        • Sanofi and GSK to seek regulatory authorization for COVID-19 vaccine
        • Press Release: Dupixent® (dupilumab) approved by European Commission for children aged 6 to 11 years with severe asthma with type 2 inflammation
        • Press Release: Strong 2021 sales and business EPS growth enabling increased investment in R&D
        • Nexviazyme® (avalglucosidase alfa) shows sustained improvements in respiratory function and mobility in patients with Pompe disease
        • CHMP recommends approval of Dupixent® (dupilumab) for children aged 6 to 11 years with severe asthma with type 2 inflammation
        • Sanofi completes acquisition of Amunix
        • Second positive Phase 3 Dupixent® (dupilumab) trial confirms significant improvements for patients with prurigo nodularis
        • FDA approves Enjaymo™ (sutimlimab-jome), first treatment for use in patients with cold agglutinin disease
        • Sanofi’s Board of Directors proposes the appointment of Carole Ferrand, Emile Voest and Antoine Yver as independent Directors
        • Media Update: Rezurock® (belumosudil) patient-reported outcomes correlated with clinical response in chronic graft-versus-host disease
        • Press Release: Annual General Meeting of May 3, 2022
        • Press Release: Foundation S: Sanofi’s new philanthropic spearhead
        • Press Release: Update on Cialis® Rx-to-OTC Switch Actual Use Trial
        • Press Release: Sarclisa® (isatuximab) combination provides unprecedented median progression free survival in patients with relapsed multiple myeloma receiving a proteasome inhibitor therapy
        • Press Release: FDA grants efanesoctocog alfa Breakthrough Therapy designation for hemophilia A
        • Press Release: New nirsevimab data analyses reinforce efficacy against RSV
        • Press Release: Annual General Meeting of May 3, 2022
        • Press Release: FDA approves Dupixent® (dupilumab) as first treatment for adults and children aged 12 and older with eosinophilic esophagitis
        • Media Update: New data from fast-growing innovative Oncology pipeline and portfolio to be presented at 2022 ASCO Annual Meeting
        • Press Release: Sanofi grants Regeneron worldwide exclusive license rights to Libtayo® (cemiplimab)
        • Media Update: CHMP recommends approval of Xenpozyme® (olipudase alfa), the first and only treatment for ASMD
        • Press Release: FDA accepts Dupixent® (dupilumab) for priority review in adults with prurigo nodularis
        • Sanofi launches 2022 global Employee Stock Purchase Plan for 86.000 people
        • Press Release: FDA approves Dupixent® (dupilumab) as first biologic medicine for children aged 6 months to 5 years with moderate-to-severe atopic dermatitis
        • Sanofi launches its first Digital Accelerator fueled by new talent and focused on growth
        • Media Update: Sanofi, a leader in immune-mediated rare blood disorders, to present latest data at EHA 2022
        • Press Release: Sanofi-GSK next-generation COVID-19 booster delivers strong immune response against variants of concern, including Omicron
        • Press Release: Sanofi-GSK first to report a successful efficacy study against Omicron with COVID-19 Beta-containing vaccine
        • Availability of the Q2 2022 Memorandum for modelling purposes
        • Media Update: Survey: Physicians and pharmacists would tell CDC to recommend vaccine like Fluzone High-Dose Quadrivalent (Influenza Vaccine) for people 65 years and older
        • Press Release: Nexviadyme® (avalglucosidase alfa) approved by European Commission as a potential new standard of care for the treatment of Pompe Disease
        • Press Release: Xenpozyme® (olipudase alfa) approved by European Commission as first and only treatment for ASMD
        • Media Update: Patient enrollment of phase III tolebrutinib trials paused in the U.S.
        • Sanofi Global Health launches nonprofit Impact® brand for 30 medicines in low-income countries
        • Press Release: Fitusiran prophylaxis reduced bleeds by 61% in people with hemophilia A or B, with or without inhibitors, compared to prior factor or bypassing agent prophylaxis
        • Press Release: Pivotal data demonstrate once-weekly efanesoctocog alfa provides superior bleed protection compared to prior factor prophylaxis
        • Press Release: Dupixent® (dupilumab) Phase 3 trial shows positive results in children 1 to 11 years of age with eosinophilic esophagitis
        • Press Release: Strong execution in Q2 drives full-year 2022 guidance upgrade and delivers rich R&D news flow in Immunology and Rare Disease
        • Press Release: Sanofi and Innovent Biologics enter strategic collaboration to accelerate development of oncology medicines and expand presence in China
        • Media Update: Tolebrutinib clinical trial program update
        • Sanofi Media Update
        • Press Release: Sanofi provides update on amcenestrant clinical development program
        • Media Update: New Dupixent® (dupilumab) data at ERS adds to body of safety and efficacy data in chronic respiratory diseases
        • Press Release: FDA grants priority review to efanesoctocog alfa for people with hemophilia A
        • Press Release: XenpozymeTM (olipudase alfa-rpcp) approved by FDA as first disease-specific treatment for ASMD (non-CNS manifestations)
        • Press Release: Evolution of the Board of Directors
        • Press Release: Late-breaking Dupixent® (dupilumab) data at ERS 2022 show consistent efficacy and safety profile for up to two years in children aged 6 to 11 years with moderate-to-severe asthma
        • Media Update: New Dupixent® (dupilumab) data at EADV 2022 adds to body of evidence across multiple inflammatory skin diseases
        • Press Release: Dupixent® (dupilumab) late-breaking Phase 3 data at EADV 2022 showed significant improvements in signs and symptoms of prurigo nodularis
        • Media Update: Positive Dupixent® (dupilumab) Phase 3 data in children aged 6 months to 5 years with moderate-to-severe atopic dermatitis published in The Lancet
        • Press Release: CHMP recommends approval of Beyfortus® (nirsevimab) for prevention of RSV disease in infants
        • Media Update: CHMP recommends approval of Enjaymo™ (sutimlimab), first and only approved treatment for hemolytic anemia in adult patients with cold agglutinin disease
        • Press Release: Availability of the Q3 2022 Memorandum for modelling purposes
        • Press Release: Dupixent® (dupilumab) approved by FDA as the first and only treatment indicated for prurigo nodularis
      • 2021
        • 2021
        • Sarclisa® (isatuximab) trial is first Phase 3 study to meet primary endpoint of minimal residual disease negativity in transplant-eligible patients with newly diagnosed multiple myeloma
        • Vaccines Investor Event: Sanofi reiterates confidence in strong growth outlook and showcases pipeline of innovative vaccine candidates
        • Sanofi to acquire Origimm Biotechnology in first move to treat acne with vaccine-based immunotherapy
        • Data from two Phase 3 studies demonstrating fitusiran significantly reduced bleeds in people with hemophilia A or B, with or without inhibitors, were featured at ASH’s plenary and late-breaking sessions
        • New England Journal of Medicine publishes positive Phase 3 Dupixent® (dupilumab) results in children with moderate-to-severe asthma
        • Sanofi completes acquisition of Kadmon
        • Sanofi to acquire Amunix immuno-oncology pipeline with next generation Conditionally Activated Biologics
        • Positive Phase 3 Dupixent® (dupilumab) data in children 6 months to 5 years with moderate-to-severe atopic dermatitis featured in RAD 2021 late-breaking session
        • Sanofi and GSK announce positive preliminary booster data for their COVID-19 vaccine candidate and continuation of Phase 3 trial per independent Monitoring Board recommendation
        • Sanofi announces results of CHMP re-examination of the New Active Substance status for avalglucosidase alfa, a potential new standard of care for the treatment of Pompe disease
        • Sanofi invests $180 million equity in Owkin’s artificial intelligence and federated learning to advance oncology pipeline
        • EMA accepts regulatory submission for olipudase alfa, the first potential therapy for ASMD
        • Press Release: Gilles SCHNEPP takes over as Chairman of the Appointments, Governance and CSR Committee of Sanofi
        • Sanofi completes acquisition of Translate Bio, accelerating the application of mRNA in new vaccines and therapeutics
        • Sanofi: Availability of the Q2 2021 Memorandum for modelling purposes
        • Sanofi to focus its COVID-19 development efforts on the recombinant vaccine candidate
        • Sanofi: Availability of the Q3 2021 Memorandum for modelling purposes
        • Sanofi: Libtayo® (cemiplimab) approved by the European Commission as the first immunotherapy indicated for patients with advanced basal cell carcinoma
        • ESMO late-breaking data show Libtayo® (cemiplimab) and chemotherapy first-line treatment combination significantly improved overall survival in patients with advanced NSCLC
        • Second Dupixent® (dupilumab) Phase 3 eosinophilic esophagitis trial to demonstrate significant disease improvements, underscoring role of type 2 inflammation in this complex disease
        • Sanofi highlights scientific innovations in the field of rare blood disorders at ISTH 2021
        • Sanofi continues streamlining of established products with sale of dental care brands to Septodont
        • Sanofi launches its new global employee share ownership plan
        • Sanofi: Positive results from the first study of high-dose influenza vaccine with a COVID-19 mRNA booster support co-administration recommendations
        • MenQuadfi® demonstrates superior immune response against serogroup C meningococcal disease in toddlers
        • Libtayo® (cemiplimab) receives positive CHMP opinion for the treatment in Europe of two advanced cancers
        • Sanofi announces positive Phase 1/2 study interim results for its first mRNA-based vaccine candidate
        • Sanofi partnering with leading academic cooperative groups to study amcenestrant in the adjuvant setting for patients with estrogen receptor positive breast cancer
        • Sanofi and Translate Bio initiate Phase 1 clinical trial of mRNA influenza vaccine
        • European Commission approves Aubagio® (teriflunomide) as the first oral MS therapy for first-line treatment of children and adolescents living with relapsing-remitting multiple sclerosis
        • FDA approves Nexviazyme® (avalglucosidase alfa-ngpt), an important new treatment option for late-onset Pompe disease
        • Sanofi and GSK initiate global Phase 3 clinical efficacy study of COVID-19 vaccine candidate
        • New, late-breaking data at EADV highlights emerging clinical profile of amlitelimab (formerly KY1005) in adults with inadequately controlled moderate-to-severe atopic dermatitis
        • Sanofi: Libtayo® (cemiplimab) approved by the European Commission for first-line treatment of patients with advanced non-small cell lung cancer with ≥50% PD-L1 expression
        • Dupixent® (dupilumab) pivotal trial meets all primary and secondary endpoints becoming first biologic medicine to significantly reduce signs and symptoms of moderate-to-severe atopic dermatitis in children as young as 6 months
        • Sanofi: Strong Q3 performance drives guidance upgrade to around 14% business EPS growth at CER(1)
        • Sanofi and GSK COVID-19 vaccine candidate demonstrates strong immune responses across all adult age groups in Phase 2 trial
        • New long-term data reinforcing promising safety and efficacy profile of brain-penetrant tolebrutinib presented at ECTRIMS 2021 
        • Sanofi provides update on Aubagio® (teriflunomide) submission for children and adolescents with relapsing-remitting multiple sclerosis in the U.S.
        • Sanofi to acquire Translate Bio; advances deployment of mRNA technology across vaccines and therapeutics development
        • FDA expands approval of Dupixent® (dupilumab) to include children aged 6 to 11 years with moderate-to-severe asthma
        • Update from Sanofi regarding Kevzara® (sarilumab): Supply constraints anticipated until early 2022
        • Early amcenestrant data featured at ASCO support its potential to become a new endocrine backbone therapy for ER+/HER2- breast cancer
        • Dupixent® (dupilumab) is the first biologic to significantly reduce itch and skin lesions in Phase 3 trial for prurigo nodularis, demonstrating the role of type 2 inflammation in this disease
        • New pivotal data at EHA 2021 reinforces sutimlimab as a first-in-class investigational C1s inhibitor with the potential to be the first approved treatment for hemolysis in people with CAD, a serious and chronic autoimmune hemolytic anemia  
        • New Soliqua® data shows improved blood sugar control without weight gain versus premixed insulin
        • Nirsevimab shows positive topline results in RSV Phase 2/3 MEDLEY trial
        • Dupixent® (dupilumab) efficacy and quality of life data in asthma patients across multiple age groups to be presented at 2021 ERS international congress
        • Sanofi provides update on Phase 3 study evaluating rilzabrutinib for the treatment of pemphigus
        • Phase 3 trial of Libtayo® (cemiplimab) combined with chemotherapy stopped early due to significant improvement in overall survival in patients with first-line advanced non-small cell lung cancer
        • Dupixent® (dupilumab) significantly improved itch and hives in patients with chronic spontaneous urticaria, a step forward in demonstrating the role of type 2 inflammation in these patients  
        • Sanofi to showcase data from its transformative oncology pipeline at 2021 ASCO Meeting
        • New Dupixent® (dupilumab) data in patients as young as 6 years old with moderate-to-severe atopic dermatitis to be presented at WCPD and EADV
        • Sanofi streamlines Consumer Healthcare portfolio in Latin America with divestiture of eight brands to Hypera Pharma
        • Sanofi announces Paris 2024 Premium partnership for the Olympic and Paralympic Games in Paris
        • New research presented at IDWeek 2021 reinforces Sanofi’s robust vaccines pipeline and commitment to advancing public health protection
        • Sanofi launches dedicated vaccines mRNA Center of Excellence
        • Sanofi provides update on venglustat clinical program
        • Dupixent® (dupilumab) SmPC updated with long-term data reinforcing well-established safety profile in adults with moderate-to-severe atopic dermatitis
        • Sanofi launches €3 million Planet Mobilization fund to support employees’ environmental projects
        • Sanofi streamlines Consumer Healthcare portfolio in Europe with divestiture of 16 brands to STADA
        • Sanofi appoints new leaders to Executive Committee and announces future Chair of EUROAPI
        • Sanofi to acquire Kadmon to further strengthen growth of transplant business
        • US FDA approves fexinidazole as the first all-oral treatment for sleeping sickness
        • New data in blood cancers, hemophilia, and other hematological disorders to be presented at ASH 2021
        • Conversion of Kiadis to a private limited liability company postponed until completion of statutory buy-out proceedings
        • Sanofi provides update on avalglucosidase alfa EU submission for patients with Pompe Disease
        • Online availability of Sanofi’s half-year financial report for 2021
        • Sales growth accelerated - Full-year guidance raised
        • Pivotal data at ATS 2021 show Dupixent® (dupilumab) significantly reduced asthma attacks and improved lung function in children
        • Sanofi and GSK initiate new Phase 2 study of their adjuvanted recombinant protein-based COVID-19 vaccine candidate
        • Sanofi to provide manufacturing support to Johnson & Johnson for their COVID-19 vaccine to help address global supply demands
        • Sanofi declares the offer for Kiadis unconditional
        • New indication for Plavix® (clopidogrel) now approved in the European Union
        • Sanofi establishes three-year collaboration with Stanford Medicine to accelerate immunology research
        • Positive Phase 3 Libtayo® (cemiplimab) results in advanced cervical cancer presented at ESMO Virtual Plenary
        • Delisting of Kiadis will be effective on 25 May 2021
        • European Commission approves second indication of Sarclisa® (isatuximab) for relapsed multiple myeloma
        • Interim late-breaking clinical data validate not-alpha profile of THOR-707 (SAR444245), Sanofi’s novel investigational IL-2
        • Sanofi presents amended protocols in fitusiran clinical studies at EAHAD 2021
        • FDA approves Libtayo® (Cemiplimab-rwlc) as first immunotherapy indicated for patients with advanced basal cell carcinoma
        • CHMP recommends approval of Sarclisa® (isatuximab) in combination with carfilzomib and dexamethasone for the treatment of relapsed multiple myeloma
        • FDA accepts Dupixent® (dupilumab) for review in children with moderate-to-severe asthma
        • Sanofi to provide support to BioNTech in manufacturing their COVID-19 vaccine to help address public health needs
        • Sanofi’s Board of Directors proposes the appointment of Christian Brandts and Barbara Lavernos as Board Members
        • New data to be featured at EHA 2021 Congress highlight Sanofi’s ongoing commitment to rare blood disorders
        • Sanofi continued its growth trajectory. Strong increase in Q1 2021 business EPS(1) at CER
        • Sanofi to build new facility in Canada to increase global availability of high-dose influenza vaccine
        • Sanofi to help manufacture Moderna COVID-19 vaccine, supporting global supply demands
        • Sanofi to invest in a leading-edge production site in Singapore; continues to strengthen its vaccines manufacturing capacities
        • FDA approves Libtayo® (cemiplimab-rwlc) monotherapy for patients with first-line advanced non-small cell lung cancer with PD-L1 expression of ≥50%
        • Positive results from the sutimlimab pivotal trial for people with cold agglutinin disease published in New England Journal of Medicine
        • Capital Markets Day 2021: Sanofi progresses on its strategy to drive growth across its businesses and innovation with emerging leadership in immunology
        • Sanofi delivered close to double-digit Q4 2020 business EPS(1) growth at CER
        • Sanofi expands its social commitments, creates nonprofit unit to provide poorest countries with access to essential medicines
        •  Data presented at WORLDSymposiumTM reinforces robust rare disease pipeline and highlights additional clinical data for investigational avalglucosidase alfa in Pompe disease
        • Sanofi completes Kymab acquisition
        • Filing of the 2020 U.S. Form 20-F and French “Document d’Enregistrement Universel” containing the Annual Financial Report
        • Sanofi completes Kiadis acquisition
        • Sanofi and Translate Bio initiate Phase 1/2 clinical trial of mRNA COVID-19 vaccine candidate
        • Sanofi to acquire Kymab, adding KY1005 to its pipeline, a human monoclonal antibody targeting key immune system regulator OX40L
        • SANOFI unveils EUROAPI as the name of the new industry leading European API* company and appoints Karl Rotthier as its future Chief Executive Officer
        • Nirsevimab demonstrated protection against respiratory syncytial virus disease in healthy infants in Phase 3 trial
        • Annual General Meeting of April 30, 2021
        • Final results of the Offer for Kiadis: 97.39% of Kiadis Shares in total committed under the Offer
        • Sanofi continues streamlining of established products with sale of anti-inflammatory drugs to Fidia Farmaceutici
        • Sanofi acquires Tidal Therapeutics, adding innovative mRNA-based research platform with applications in oncology, immunology, and other disease areas
        • New Dupixent® (dupilumab) data showcasing improvements across four type 2 inflammatory diseases to be presented at 2021 AAAAI Annual Meeting
        • Efanesoctocog alfa granted FDA Fast Track Designation for treatment of hemophilia A
        • Availability of the Q1 2021 Memorandum for modelling purposes
        • Offer Memorandum for All Outstanding Shares of Kiadis Pharma N.V.
        • Sanofi launches recommended cash offer for all shares in Kiadis
        • The Lancet publishes Libtayo® (cemiplimab) data showing extended overall survival in patients with first-line advanced non-small cell lung cancer with PD-L1 expression of ≥50%
        • FDA approves Sarclisa® (isatuximab) in combination with carfilzomib and dexamethasone for patients with relapsed or refractory multiple myeloma
        • Phase 3 trial of Libtayo® (cemiplimab) monotherapy in advanced cervical cancer stopped early for positive result on overall survival           
        • Kiadis shareholders give irrevocable commitment to tender 36.6% of the shares under the offer by Sanofi
        • New Dupixent® (dupilumab) analyses reinforce long-term safety and efficacy profile in patients with atopic dermatitis as young as 6 years
        • Sanofi and GSK initiate global Phase 3 clinical efficacy study of COVID-19 vaccine candidate
      • 2020
        • 2020
        • Sanofi and Kiadis satisfy competition condition related to the tender offer
        • Sanofi pioneers sustainable finance in the pharmaceutical industry with the signing of its two first sustainability-linked revolving credit facilities
        • Update on the intended offer by Sanofi for Kiadis
        • CHMP recommends approval of Plavix® (clopidogrel) with aspirin in adults for certain types of strokes
        • Dupixent® (dupilumab) approved by European Commission as first and only biologic medicine for children aged 6 to 11 years with severe atopic dermatitis
        • Sanofi renews partnership with the WHO to fight Neglected Tropical Diseases and eliminate sleeping sickness before 2030
        • FDA grants priority review for avalglucosidase alfa, a potential new therapy for Pompe disease
        • Sanofi to resume dosing in fitusiran clinical studies in the U.S.
        • Rilzabrutinib granted FDA Fast Track Designation for treatment of immune thrombocytopenia
        • European Commission approves Supemtek® (quadrivalent recombinant influenza vaccine) for the prevention of influenza in adults aged 18 years and older
        • FDA issues Complete Response Letter for sutimlimab, an investigational treatment for hemolysis in adults with cold agglutinin disease
        • Sanofi and GSK announce a delay in their adjuvanted recombinant protein-based COVID-19 vaccine program to improve immune response in the elderly
        • Availability of the Q4 2020 Memorandum for modelling purposes
        • European Commission approves MenQuadfi®, the latest innovation in meningococcal (MenACWY) vaccination for individuals 12 months of age and older
        • Sanofi to commence tender offer for acquisition of Principia Biopharma Inc.
        • Availability of the Pre-quarterly Results Communication
        • Sanofi to present Phase 3 results of avalglucosidase alfa in patients with late-onset Pompe disease
        • FDA grants Dupixent® (dupilumab) Breakthrough Therapy designation for eosinophilic esophagitis
        • Sanofi H1 2020 business EPS(1) growth of 9.2%(2) driven by transformation
        • Sanofi and GSK selected for Operation Warp Speed to supply United States government with 100 million doses of COVID-19 vaccine
        • Sanofi provides update on Kevzara® (sarilumab) Phase 3 trial in severe and critically ill COVID-19 patients outside the U.S.
        • Sanofi and GSK agree with the UK government to supply up to 60 million doses of COVID-19 vaccine
        • Sanofi’s investigational enzyme replacement therapy shows clinically meaningful improvement in critical manifestations of late-onset Pompe disease
        • Sanofi and GSK will provide up to 300 million doses of COVID-19 vaccine to the European Union
        • Sanofi and GSK in advanced discussions with European Union to supply up to 300 million doses of COVID-19 vaccine
        • CHMP recommends approval of MenQuadfi® for active immunization of individuals from the age of 12 months and older against invasive meningococcal ACWY disease
        • Sanofi to evaluate the safety and efficacy of novel investigational candidate THOR-707 and KEYTRUDA® (pembrolizumab) in pursuit of establishing a new treatment option in oncology
        • Sanofi to launch “Action 2020”, a worldwide employee stock purchase plan
        • Dupixent® (dupilumab) approved in China for adults with moderate-to-severe atopic dermatitis
        • Hart-Scott-Rodino waiting period expires for Sanofi’s acquisition of Principia Biopharma Inc.
        • EMA accepts regulatory submission for avalglucosidase alfa, a potentially new standard of care enzyme replacement therapy for Pompe disease
        • Sanofi offers to acquire Kiadis, a clinical-stage company developing cell-based immunotherapy products
        • CHMP recommends approval of Dupixent® (dupilumab) for children aged 6 to 11 years with severe atopic dermatitis
        • Sanofi and Translate Bio mRNA COVID-19 vaccine candidate induced high antibody levels in preclinical studies
        • Sanofi and GSK to support COVAX with 200 million doses of adjuvanted, recombinant protein-based COVID-19 vaccine
        • New England Journal of Medicine publishes positive final results from Phase 1/2a study of BIVV001 in people with severe hemophilia A
        • European Commission approves Sarclisa® (isatuximab) for adults with relapsed and refractory multiple myeloma
        • Sanofi completes Principia Biopharma Inc. acquisition
        • Dupixent® (dupilumab) significantly reduced severe asthma attacks in children and is the only biologic to demonstrate improvement in children’s lung function in a randomized Phase 3 trial
        • Sarclisa® (isatuximab) combination therapy demonstrated superior progression free survival and clinically meaningful depth of response in patients with relapsed multiple myeloma
        • Sanofi offers to acquire Kiadis for €308 million
        • Late-breaking ESMO presentation shows Libtayo® (cemiplimab) monotherapy increases overall survival in first-line advanced non-small cell lung cancer with PD-L1 expression of ≥50%
        • Sanofi invests to make France its world class center of excellence in vaccine research and production
        • Sanofi Q3 2020 business EPS(1) growth of 8.8% at CER
        • Dupixent® (dupilumab) long-term data show sustained improvement in lung function and reduction in severe exacerbations in adults and adolescents with moderate-to-severe asthma
        • Dupixent® (dupilumab) late-breaking pivotal data showing significant improvement in eosinophilic esophagitis signs and symptoms presented for the first time at scientific meetings
        • Sanofi announces closing of Regeneron stock sale
        • New clinical and health-related quality of life data in multiple myeloma and rare blood disorders to be presented at ASH 2020
        • Safety and efficacy of Dupixent® (dupilumab) in patients as young as 6 years with moderate-to-severe atopic dermatitis further reinforced by new data analyses presented at EADV
        • Sanofi’s virtual R&D Day event to highlight capabilities, platforms, and expertise in disease pathways to deliver potentially transformative treatments to patients
        • Sanofi to present growth opportunities and development strategy for Dupixent® (dupilumab) in type 2 inflammatory diseases
        • CHMP recommends approval of Supemtek® (quadrivalent recombinant influenza vaccine) for the prevention of influenza in adults aged 18 years and older
        • European Patent Office rules in favor of Sanofi and Regeneron concerning Praluent® (alirocumab)
        • Positive pivotal data for Libtayo® (cemiplimab) monotherapy in locally advanced basal cell carcinoma featured as a late-breaking presentation at ESMO 
        • Online availability of Sanofi’s half-year financial report for 2020
        • Sanofi to acquire Principia Biopharma
        • Dr. Jean-Christophe Rufin appointed President of the Sanofi Espoir Corporate Foundation
        • Sanofi and GSK initiate Phase 1/2 clinical trial of COVID-19 adjuvanted recombinant protein-based vaccine candidate
        • Sanofi announces positive long-term efficacy and safety data for fitusiran from interim analysis of Phase 2 extension study in people with hemophilia A and B, with or without inhibitors 
        • Availability of the Q3 2020 Memorandum for modelling purposes
        • Sanofi and Regeneron provide update on Kevzara® (sarilumab) Phase 3 U.S. trial in COVID-19 patients
        • Sanofi and GSK sign agreements with the Government of Canada to supply up to 72 million doses of adjuvanted COVID-19 vaccine
        • Nirsevimab reduced respiratory syncytial virus infections requiring medical care in healthy premature infants in Phase 2b trial
        • Sanofi to present oncology strategy, provide update on portfolio and emerging pipeline
        • Sanofi and Translate Bio expand collaboration to develop mRNA vaccines across all infectious disease areas
        • Sanofi : FDA approves Sarclisa® (isatuximab-irfc) for patients with relapsed refractory multiple myeloma
        • COVID-19:  Sanofi to donate 100 million doses of hydroxychloroquine across 50 countries 
        • Sanofi : Filing of the 2019 U.S. Form 20-F and French “Document d’Enregistrement Universel” containing the Annual Financial Report
        • Sanofi : Availability of the Pre-quarterly Results Communication
        • Sanofi announces pricing of Regeneron stock offering
        • Sanofi: FDA approves Dupixent® (dupilumab) as first biologic medicine for children aged 6 to 11 years with moderate-to-severe atopic dermatitis
        • Sanofi joins forces with U.S. Department of Health and Human Services to advance a novel coronavirus vaccine
        • Sanofi: First patient outside U.S. treated in global Kevzara® (sarilumab) clinical trial program for patients with severe COVID-19
        • Sanofi to present Phase 2 detailed results of its brain-penetrant BTK inhibitor in relapsing multiple sclerosis
        • Sanofi and Translate Bio collaborate to develop novel mRNA vaccine candidate against COVID-19
        • Sanofi: Annual General Meeting of April 28, 2020
        • Libtayo® (cemiplimab) shows clinically meaningful and durable responses in second-line advanced basal cell carcinoma
        • Sanofi's Board of Directors proposes the appointment of Rachel Duan and Lise Kingo as independent directors
        • Sanofi to highlight pipeline programs in a series of interactive virtual sessions leading to a R&D day event
        • Sanofi delivers strong 2019 business EPS growth of 6.8% at CER
        • Sanofi: Phase 3 trial of Libtayo® (cemiplimab) as monotherapy for first-line advanced non-small cell lung cancer stopped early due to highly significant improvement in overall survival
        • Sanofi and GSK to join forces in unprecedented vaccine collaboration to fight COVID-19
        • Sanofi names new leaders to Executive Committee
        • Sanofi: Availability of the Pre-quarterly Results Communication
        • Sanofi brain-penetrant BTK inhibitor significantly reduced disease activity in Phase 2 trial in relapsing multiple sclerosis
        • Libtayo® (cemiplimab-rwlc) longer-term results in advanced cutaneous squamous cell carcinoma presented at ASCO 2020 show durable responses that deepen over time
        • FDA approves MenQuadfiTM, the latest innovation in meningococcal (MenACWY) vaccination
        • Sanofi successfully prices EUR 1.5 billion of bond issue
        • Sanofi receives positive CHMP opinion for Sarclisa® (isatuximab) for the treatment of relapsed and refractory multiple myeloma
        • Sanofi : Positive topline results demonstrated by olipudase alfa, first and only investigational therapy in late-stage development for acid sphingomyelinase deficiency
        • Sanofi and Regeneron provide update on U.S. Phase 2/3 adaptive-designed trial in hospitalized COVID-19 patients
        • Sanofi: Dupixent® (dupilumab) Phase 3 data show significant improvement in severe atopic dermatitis for children aged 6 to 11 years
        • Sanofi successfully prices taps on outstanding bond issues for EUR 500 million
        • Sanofi: Information on Sanofi’s Shareholder General Meeting of Tuesday, April 28, 2020
        • Sarclisa® (isatuximab) Phase 3 IKEMA trial meets primary endpoint early in patients with relapsed multiple myeloma
        • Sanofi’s Board of Directors notes the resignation of Emmanuel Babeau and coopts Gilles Schnepp as Independent Director
        • FDA grants priority review of sutimlimab, potential first approved treatment of hemolysis in adult patients with Cold Agglutinin Disease
        • Sanofi : FDA accepts for priority review Dupixent® (dupilumab) for children aged 6 to 11 years with moderate-to-severe atopic dermatitis
        • Sanofi intends to sell its equity investment in Regeneron; confirms no change to ongoing collaboration
        • Sanofi and Luminostics to join forces on developing breakthrough COVID-19 smartphone-based self-testing solution
        • Sanofi finalizes Praluent® (alirocumab) restructuring with Regeneron
        • Dupixent® (dupilumab) eosinophilic esophagitis trial meets both co-primary endpoints
        • Sanofi to create new industry leading European company to provide active pharmaceutical ingredients (API*)
        • Sanofi : Sanofi brain-penetrant BTK inhibitor meets primary endpoint of Phase 2 trial in relapsing multiple sclerosis
        • Sanofi : Sanofi Completes Acquisition of Synthorx, Inc.
        • Sanofi : Hart-Scott-Rodino waiting period expires for Sanofi’s acquisition of Synthorx
      • 2019
        • 2019
        • Sanofi commences tender offer for acquisition of Synthorx, Inc.
        • Sanofi Q3 well on track
        • Sanofi : Positive results in Phase 3 trial for Toujeo® in children and adolescents with type 1 diabetes
        • Sanofi and Regeneron announce intent to restructure Antibody collaboration for Kevzara® (sarilumab) and Praluent® (alirocumab)
        • Sanofi : FDA approves Fluzone® High-Dose Quadrivalent (Influenza Vaccine) for adults 65 years of age and older
        • Sanofi : Dupixent® (dupilumab) now approved in European Union for severe chronic rhinosinusitis with nasal polyposis
        • Sanofi announces settlement agreement related to Contingent Value Rights (CVRs) Litigation
        • Sanofi : Positive results presented from pivotal Phase 3 trial of sutimlimab in people with cold agglutinin disease
        • Sanofi : Sanofi to acquire Synthorx to bolster its immuno-oncology pipeline for $2.5 Billion
        • Sanofi CEO unveils new strategy to drive innovation and growth
        • Sanofi opens its first digitally-enabled, continuous manufacturing facility; ushers in next generation of biotech manufacturing
        • Sanofi : CHMP recommends approval of Dupixent® (dupilumab) for moderate-to-severe atopic dermatitis in adolescents
        • Sanofi : FDA approves Dupixent® (dupilumab) for chronic rhinosinusitis with nasal polyposis
        • Sanofi: Positive results presented from two Phase 3 trials of Dupixent® (dupilumab) in severe chronic rhinosinusitis with nasal polyps
        • Sanofi: Filing of the 2018 U.S. Form 20-F and French « Document de Référence » containing the Annual Financial Report
        • Sanofi: FDA to undertake priority review of Dupixent® (dupilumab) for adults with inadequately controlled severe chronic rhinosinusitis with nasal polyps
        • Sanofi: Fexinidazole, the first all-oral treatment for sleeping sickness, approved in Democratic Republic of Congo
        • Sanofi: CHMP recommends approval of Dupixent® (dupilumab) for asthma indication
        • Sanofi : Dupixent® (dupilumab) approved by European Commission for adolescents with moderate-to-severe atopic dermatitis
        • Sanofi's Board of Directors notes the resignation of Christian Mulliez and co-opts Christophe Babule as Director
        • Sanofi signs strategic deal for exclusive US over-the-counter rights to Tamiflu® in Flu Care
        • Sanofi : CHMP recommends ZynquistaTM (sotagliflozin) for the treatment of adults with type 1 diabetes
        • Sanofi : Dupixent® (dupilumab) showed positive topline results in Phase 3 trial of children aged 6 to 11 years with severe atopic dermatitis
        • Sanofi : CHMP recommends approval of Dupixent® (dupilumab) for severe chronic rhinosinusitis with nasal polyposis  
        • Sanofi : Libtayo® (cemiplimab) approved for advanced cutaneous squamous cell carcinoma in the European Union
        • Sanofi : FDA to review isatuximab as a potential treatment for relapsed/refractory multiple myeloma
        • CHMP issues positive opinion for Libtayo® (cemiplimab) in advanced cutaneous squamous cell carcinoma
        • Sanofi appoints Ameet Nathwani Chief Digital Officer
        • Phase 3 trial of isatuximab combination therapy showed 40% reduction in the risk of disease progression or death for patients with relapsed/refractory multiple myeloma
        • Sanofi : CHMP recommends approval of Praluent® (alirocumab) to reduce cardiovascular risk in people with established atherosclerotic cardiovascular disease
        • Sanofi and Abbott partner to integrate glucose sensing and insulin delivery technologies to help change the way diabetes is managed
        • Sanofi :  Sanofi provides update on ZynquistaTM (sotagliflozin) type 2 diabetes Phase 3 program and collaboration with Lexicon
        • Sanofi: Annual General Meeting of April 30, 2019
        • Sanofi : Availability of the Pre-quarterly Results Communication
        • Sanofi: FDA advisory committee votes on Zynquista(TM) (sotagliflozin) as treatment for adults with type 1 diabetes
        • Sanofi and Regeneron announce positive topline Phase 2 results for IL-33 antibody in asthma
        • Sanofi: FDA issues Complete Response Letter for Zynquista(TM) (sotagliflozin)
        • Sanofi : New England Journal of Medicine publishes data showing improved survival with Jevtana® (cabazitaxel) over second androgen receptor-targeted agent in metastatic castration-resistant prostate cancer
        • Sanofi and Google to develop new healthcare Innovation Lab
        • Sanofi : Online Availability of Sanofi Group’s Half-Year Financial Report for 2019
        • Sanofi successfully prices EUR 2 billion of bond issues
        • Sanofi : Availability of the Pre-quarterly Results Communication
        • Sanofi : Isatuximab Phase 3 trial meets primary endpoint of prolonging progression free survival in patients with relapsed/refractory multiple myeloma
        • Sanofi : Sanofi and Regeneron strongly disagree with verdict upholding three of five Amgen U.S. patent claims relating to PCSK9 antibodies
        • Sanofi delivered solid growth in Q2 2019
        • Sanofi : Dupixent® (dupilumab) Approved for Severe Asthma by European Commission
        • Soliqua® Phase 3 results significantly lowered blood sugar levels compared to GLP-1 receptor agonist treatments
        • Sanofi: FDA approves Cablivi® (caplacizumab-yhdp), the first Nanobody®-based medicine, for adults with acquired thrombotic thrombocytopenic purpura (aTTP)
        • Sanofi: Availability of the Pre-quarterly Results Communication
        • ZynquistaTM now approved in the European Union for treatment of adults with type 1 diabetes
        • Sanofi: FDA approves Praluent® (alirocumab) to prevent heart attack, stroke and unstable angina requiring hospitalization
        • Sanofi delivers 2018 business EPS growth of 5.1% at CER
        • Paul Hudson to succeed Olivier Brandicourt as Chief Executive Officer
        • Sanofi: Sanofi and Alnylam conclude research and option phase of 2014 rare disease alliance
        • Sanofi: Availability of the Pre-quarterly Results Communication
        • Praluent® (alirocumab) now approved in European Union to reduce the risk of cardiovascular events in patients with established cardiovascular disease
        • Sanofi : FDA to review MenQuadfi, a meningococcal vaccine candidate
        • Sanofi : Information on the departure conditions of Olivier Brandicourt, Chief Executive Officer
        • Sanofi : U.S. District Court invalidates Amgen patent claims targeting PCSK9
        • Sanofi delivers strong Q1 2019 business EPS growth of 9.4% at CER
        • New England Journal of Medicine publishes positive results of the pivotal trial of Cablivi® (caplacizumab) for rare blood clotting disorder
        • Sanofi and Regeneron Restructure Immuno-Oncology Collaboration for Discovery and Development Programs
      • 2018
        • 2018
        • Sanofi Head of Global R&D Elias Zerhouni to retire; Company names John Reed to take over on July 1
        • FDA grants priority review for Dupixent® (dupilumab) as potential treatment for adolescents with uncontrolled moderate-to-severe atopic dermatitis
        • Information concerning the total number of voting rights and shares, provided pursuant to article L. 233-8 II of the Code de commerce (the French Commercial Code) and article 223-16 of the Règlemen...
        • Sanofi: FDA Approves VAXELIS(TM), Sanofi and MSD's Pediatric Hexavalent Combination Vaccine
        • Sanofi appoints Jean-Baptiste Chasseloup de Chatillon Executive Vice President, Chief Financial Officer
        • Sanofi: Dupixent® (dupilumab) showed positive Phase 3 results in adolescents with inadequately controlled moderate-to-severe atopic dermatitis
        • Sanofi : Sanofi and Advent finalize negotiations for the acquisition of Zentiva
        • Sanofi: New England Journal of Medicine publishes pivotal cemiplimab trials showing positive results in advanced cutaneous squamous cell carcinoma
        • Sanofi : Sanofi successfully prices USD 2 billion bond issue
        • Sanofi and Ablynx Announce the Successful Results of the Initial Tender Offer Period for Ablynx and Commencement of Squeeze-Out Tender Period
        • Sanofi: EMA to review sotagliflozin as potential treatment for type 1 diabetes
        • Sanofi: European Medicines Agency recommends fexinidazole, the first all-oral treatment for sleeping sickness
        • Sanofi and Ablynx Announce the Successful Results of the Initial Tender Offer Period for Ablynx and Commencement of Squeeze-Out Tender Period
        • FDA to review supplemental Biologics License Application for Praluent® (alirocumab) Injection as potential treatment to reduce major adverse cardiovascular events
        • Sanofi: Cablivi(TM) (caplacizumab) approved in Europe for adults with acquired thrombotic thrombocytopenic purpura (aTTP)
        • Sanofi successfully prices EUR 8 billion of bond issues
        • Online Availability of Sanofi Group's Half-Year Financial Report for 2018
        • Previously announced Tender Offers by Sanofi to acquire Ablynx will commence on April 4, 2018
        • Sanofi reaches civil settlement with US SEC
        • New England Journal of Medicine publishes positive detailed results from Praluent® (alirocumab) cardiovascular outcomes trial
        • Sanofi Q3 2018 Performance Confirms Return to Growth
        • Sanofi: FDA to Conduct Priority Review of Cemiplimab as a Potential Treatment for Advanced Cutaneous Squamous Cell Carcinoma
        • Sanofi to invest €350 million in Canadian vaccine facility
        • Sanofi: ODYSSEY OUTCOMES investigators highlight at AHA that Praluent® (alirocumab) was associated with fewer deaths from any cause
        • Sanofi: FDA approves asthma indication for Dupixent® (dupilumab)
        • Sanofi: Positive Phase 3 results presented for Dupixent® (dupilumab)
        • Sanofi : FDA approves Libtayo® (cemiplimab) as first and only treatment for advanced cutaneous squamous cell carcinoma
        • Sanofi: First-quarter 2018 Business EPS(1) up 1.4% at CER
        • Sanofi: Dupixent® (dupilumab) showed positive topline results in two Phase 3 trials of patients with chronic rhinosinusitis with nasal polyps
        • Sanofi: CHMP recommends approval of Cablivi(TM) (caplacizumab)
        • Sanofi and Denali Therapeutics to develop treatments for neurological and inflammatory diseases
        • Sanofi: Availability of the Pre-quarterly Results Communication
        • Sanofi: Availability of the Pre-quarterly Results Communication
        • Sanofi to refocus two global business units
        • Advent International enters into exclusive negotiations to acquire Zentiva, Sanofi's European generics business
        • Sanofi to Transfer U.S. Stock Exchange Listing to Nasdaq
        • Sanofi: Availability of the Pre-quarterly Results Communication
        • Sanofi: Q2 2018 Performance Positions Sanofi for New Growth Phase
        • Sanofi: Annual General Shareholders' Meeting of May 2, 2018
        • Sanofi Launches "Action 2018", a Worldwide Employee Stock Purchase Plan
        • Sanofi completes divestiture of Zentiva to Advent
        • Dengvaxia® vaccine approved for prevention of dengue in Europe
        • Sanofi: New England Journal of Medicine publishes two positive Phase 3 trials showing Dupixent® (dupilumab) improved moderate-to-severe asthma
        • Sanofi Head of Human Resources Roberto Pucci to retire; Company names Caroline Luscombe to take over October 1st
        • Sanofi receives positive CHMP opinion for dengue vaccine
        • Sanofi : Sanofi completes its acquisition of Ablynx following the expiration of the Squeeze-out Procedure
        • Sanofi: EMA to review Dupixent® (dupilumab) as potential treatment for inadequately controlled moderate-to-severe asthma
        • Sanofi: EMA to review cemiplimab as a potential treatment for advanced cutaneous squamous cell carcinoma
        • Sanofi: Availability of the Pre-quarterly Results Communication
        • Sanofi to acquire Ablynx for €3.9 Billion
        • Sanofi Announces Receipt of Antitrust Clearances in Connection with the Acquisition of Ablynx
        • Sanofi Commences Tender Offer for Acquisition of Bioverativ Inc.
        • Sanofi Completes Acquisition of Bioverativ Inc.
        • Sanofi Delivers 2017 Business EPS(1) in line with Guidance
        • Sanofi: Hart-Scott-Rodino waiting period expires for Sanofi's acquisition of Bioverativ
        • Sanofi: Praluent® (alirocumab) significantly reduced risk of cardiovascular events in high-risk patients, and was associated with lower death rate
        • Sanofi Appoints Dominique Carouge Executive Vice President Head of Business Transformation and Member of the Executive Committee
        • Sanofi and Regeneron announce plans to make Praluent® more accessible and affordable for patients with the greatest health risk and unmet need
        • Sanofi: Sanofi, DNDi seek European Medicines Agency review for sleeping sickness treatment
        • 2018-01-29-08-43-24-1313336
        • Evotec and Sanofi in exclusive talks to create an Evotec-led Infectious Disease open innovation R&D platform
        • Sanofi to Acquire Bioverativ for $11.6 Billion
        • Sanofi's Board of Directors Proposes Appointment of Emmanuel Babeau as New Independent Director
        • Sanofi : FDA to review Dupixent® (dupilumab) as potential treatment for moderate-to-severe asthma
        • Sanofi and Alnylam enter into strategic restructuring of RNAi therapeutics rare disease alliance
        • Sanofi and Regeneron to accelerate and expand investment for cemiplimab and dupilumab development programs
        • Sanofi: Filing of the 2017 U.S. Form 20-F and French « Document de Référence » containing the Annual Financial Report
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