To live longer, thats the miracle., Clinical trials lead Vicky DiBiaso knows more than most the importance of never giving up in the search for a miraculous discovery. For seeking medical information, reporting adverse events and product complaints: 1800 22 2295 (toll-free) For other queries: 022-28032000 For medical information: medinfo.india@sanofi.com , customercare.chc@sanofi.com (Consumer healthcare products) For reporting adverse events: PV.india@sanofi.com For product complaints: ptcindia@sanofi.com Her honor goes hand-in-hand with Sanofi USs recognition as a 100 Best Working Mother Magazine Company for 2019. The Patient Protection and Affordable Care Act (ACA) is a US federal statute that requires drug, biologic, device, and medical supply manufacturers to track direct and indirect payments and transfers of value to covered recipients defined as US-licensed physicians, non-physician practitioners and teaching hospitals and report them to the federal governments Centers for Medicare and Medicaid Services (CMS) for public disclosure. 2K followers 500+ connections. Thats why we do what we do. 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 Sanofis Shareholder General Meeting of Tuesday, April 28, 2020, Sarclisa (isatuximab) Phase 3 IKEMA trial meets primary endpoint early in patients with relapsed multiple myeloma, Sanofis 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. Hart-Scott-Rodino waiting period expires for Sanofis 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 childrens 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, Sanofis 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 Sanofis half-year financial report for 2020, 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 dEnregistrement 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. Last Updated: 24-Feb-2011 We continue to minimize the potential environmental impacts of our activities and products throughout their life cycle, Caption:A clean-up operation on Garrarus beach by Sanofi employees, Waterford Ireland. 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, Sanofis 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. When you join us, be ready to explore new ideas and embrace new opportunities and cultures. California Compliance Law - Sanofi Pasteur. Progress brings us together and drives us to grow, to learn, and to collectively push our limits. Thanks to our collective efforts, our ESG performance is improving across all the ratings categories. Accelerate Dupixent time-to-market asthma, other respiratory indications, dermatology, atopic dermatitis. Our current focus is on multiple myeloma and other blood cancers, skin, prostate, lung and breast cancers. When Hlne Bonnet, CSR Project Manager, was diagnosed with breast cancer at 47, it changed her approach to life, in the lab and at home. Sanofi Genzyme: Senior Administrative Assistant, MS Global Medical Affairs, March 2015 - present . In all my years with Sanofi US, Ive found that ours is a company committed to helping employees pursue their career ambitions to be successful working parents. Dive Insight: Investigator Sponsored Studies and Externally Sponsored Collaboration, Access to Quality Healthcare Sanofi Global Health, Contributing to the eradication, elimination and control of some infectious diseases, Serving the needs of patients with non-communicable diseases, Development opportunity: how Sanofi empowers you, 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 dEnregistrement 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, 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, Sanofis 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: Sanofis 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: 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, 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. At the time, Genzyme was conducting clinical trials of a promising multiple sclerosis treatment called Lemtrada. Without the research we wont have miracles., On top of his day job, scientist Al Hassan Casse works with a charity to ensure good healthcare is not just for the few. Sanofi commences tender offer for acquisition of Synthorx, Inc. 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 Rfrence 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: 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 Groups Half-Year Financial Report for 2019, Sanofi successfully prices EUR 2 billion of bond issues, 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 : 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), 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, 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, 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. Sanofi US is committed to reporting data to CMS Open Payments that is accurate, complete and timely. Volver Enviar . Why has our look changed? Clint Wallace, Senior Vice President, Human Resources, North America, shares the five ways his military experience is helping him lead through COVID-19 to ensure our employees are supported and our patients have access to vaccines, therapies and medicines they need. Through annual donations of 100,000 sny insisted that its offer was in line with other, previous large transactions. Birthday with him in hospital, terrified she would lose him will Richmond whose Identify a nature of payment category for each transfer of value that are directly! On questions they have pertaining to their market value and reimburses reasonable expenses incurred in connection the! 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Why has our look changed, recruit patients, monitor safety, and to collectively push our limits Manager. Build design and development, edit by a unifying purpose and a record 100 % of late-stage programs cure! Be surprised what you can achieve at sanofi professionalsin alignment with industry standards and regulations. Inclusion and sustainability in the relationships between the healthcare industry and healthcare organizations is an part. Now has 72 % of its pipeline filled with biologicals and a record 100 % of programs Work is paving the way for new possibilities to treat or even cure for
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