Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.
Company Size
10,001+
Company Stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988
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A gene therapy treatment has restored hearing in children born deaf due to inherited OTOF gene variants. In a clinical trial, nine of 12 children with profound deafness gained meaningful hearing after receiving Otarmeni (lunsotogene parvec-cwha), developed by Regeneron. The treatment delivers a working copy of the otoferlin gene directly into the cochlea using a dual AAV1 vector. By 24 weeks, four patients achieved normal to near-normal hearing, whilst four others had mild to moderate hearing loss. Cincinnati Children's Hospital treated two siblings as part of the trial. Three-year-old Abdu went from hearing virtually nothing to normal range hearing within weeks. His one-year-old sister Sumaya also showed dramatic improvement. The therapy addresses OTOF-related congenital deafness, which accounts for approximately 1% of congenital deafness cases. Results were published in The New England Journal of Medicine.
Regeneron Pharmaceuticals, Inc. announces presentation of new clinical research at European Society for Medical Oncology Congress 2026. Published on 10/06/2026 at 02:20 pm EDT S&P Capital IQ Regeneron Pharmaceuticals, Inc. announced the presentation of new clinical research at the European Society for Medical Oncology (ESMO) Congress 2026, taking place from October 23-27 in Madrid, Spain. Highlights from the company?s 10 abstracts will cover new data and analyses from trials in cutaneous squamous cell carcinoma (CSCC), non-small cell lung cancer (NSCLC), ovarian cancer, melanoma and cancer-associated thrombosis. The potential uses of neoadjuvant Libtayo in CSCC, ubamatamab, cenvacibart and amrecibart described above are investigational, and their safety and efficacy have not been evaluated by any regulatory authority. Libtayo is a fully human monoclonal antibody targeting the immune checkpoint receptor PD-1 on T cells and was invented using Regeneron's proprietary VelocImmune(R) technology. By binding to PD-1, Libtayo has been shown to block cancer cells from using the PD-1 pathway to suppress T-cell activation. Libtayo has been approved by regulatory authorities in more than 30 countries in one or more indications, including for certain adult patients with advanced basal cell carcinoma (BCC), CSCC that is advanced or at high risk of recurrence, advanced NSCLC and advanced cervical cancer. In the U.S., the generic name for Libtayo in its approved indications is cemiplimab-rwlc, with rwlc as the suffix designated in accordance with Nonproprietary Naming of Biological Products Guidance for Industry issued by the U.S. FDA. Outside of the U.S., the generic name of Libtayo in its approved indications is cemiplimab. The extensive clinical program for Libtayo is focused on difficult-to-treat cancers. Libtayo is currently being investigated in trials as a monotherapy, as well as in combination with either conventional or novel therapeutic approaches for other solid tumors. (C) S&P Capital IQ - 2026
France's Sanofi and US-based Regeneron Pharmaceuticals will expand their 20-year partnership to jointly develop and market immunology medicines in a deal worth up to $8 billion. Regeneron will receive $1 billion upfront, with potential additional payments of up to $7 billion tied to development, regulatory, and commercial targets. The collaboration will add four next-generation immunology drug candidates invented by Regeneron, with one currently in early-stage trials for eczema. The companies will equally share development costs and future profits from new drugs, whilst their existing profit-sharing agreement for top-selling medicine Dupixent remains unchanged. The deal settles prior litigation between the companies and marks an early move by Sanofi's new chief executive Belen Garijo to strengthen the company's pipeline.
Regeneron and Sanofi expand collaboration to develop long-acting immunology antibodies. Thursday, October 01, 2026 Regeneron Pharmaceuticals and Sanofi have expanded their long-standing antibody collaboration to develop and commercialise a new group of long-acting immunology treatments. Dupixent is a fully human monoclonal antibody that blocks signalling through the IL-4 and IL-13 pathways. It was developed using Regeneron's VelocImmune technology and is not an immunosuppressant. The agreement builds on more than two decades of work between the companies and their development of Dupixent (dupilumab), a widely used treatment for diseases linked to type 2 inflammation. Under the expanded agreement, the companies will jointly develop and commercialise four long-acting antibodies discovered by Regeneron. The candidates target interleukin-13 (IL-13), IL-4 and IL-4 pathways, including an IL-4xIL-13 bispecific antibody and an antibody targeting the IL-4 receptor alpha (IL-4Rα). REGN20423, an IL-13 antibody, is currently being evaluated in a Phase 1 clinical trial for atopic dermatitis. The other three antibody programmes are expected to enter clinical studies in 2027. Regeneron will also have the option to add Sanofi's investigational lunsekimig to the collaboration after completion of its Phase 3 trials in chronic obstructive pulmonary disease. Lunsekimig is a bispecific Nanobody therapy designed to target thymic stromal lymphopoietin (TSLP) and IL-13. As part of the agreement, Sanofi will pay Regeneron $1 billion upfront. Regeneron could receive up to a further $7 billion through development, regulatory and commercial milestones. The companies will share development and commercialisation costs for the new programmes and divide future profits equally worldwide. Regeneron will lead research and development activities, while Sanofi will oversee global commercialisation. The existing profit-sharing arrangement for Dupixent will remain unchanged. The companies have also resolved their previous litigation related to their collaboration. The expanded alliance continues a partnership that began in 2003. The collaboration has resulted in several approved medicines, with Dupixent becoming a major treatment for conditions associated with type 2 inflammation. More than 1.5 million people are currently receiving Dupixent worldwide. The medicine has been approved in more than 60 countries for a range of conditions, including atopic dermatitis, asthma, chronic rhinosinusitis with nasal polyps, eosinophilic oesophagitis, prurigo nodularis, chronic spontaneous urticaria, chronic obstructive pulmonary disease, bullous pemphigoid and allergic fungal rhinosinusitis, across different age groups. Regeneron and Sanofi are also evaluating dupilumab in additional conditions associated with type 2 inflammation and allergic processes. These include chronic pruritus of unknown origin. These potential uses remain under clinical investigation and have not yet been fully evaluated for safety and efficacy by regulatory authorities.
Sanofi, Regeneron expand tie-up with $8 billion drug-development deal, settle legal dispute. By Thomson Reuters Oct 1, 2026 | 1:16 AM By Bhanvi Satija and Mariam Sunny Oct 1 (Reuters) - Sanofi and Regeneron said on Thursday they will develop four new drugs together in a deal worth up to $8 billion and settle prior litigation, moves analysts said signal a reset of their strained partnership and an early win for the French drugmaker's new CEO Belen Garijo. Sanofi will pay $1 billion upfront with an additional $7 billion in potential milestone payments. The companies will equally share development costs and future profits on the four drugs, with Regeneron leading research and Sanofi handling global sales if they are approved. Sanofi shares closed up nearly 1% on Thursday. Shares of Tarrytown, New York-based Regeneron were down 4% in midday trading. "Mutual trust will be the guiding principle in this extended relationship," Garijo said on an investor call, adding that the partnership would include clear roles and accountability for both firms. Garijo, who took over the top role at Sanofi in May and is leading a strategic review of the company, has promised investors faster decision-making. Barclays analysts noted that her predecessor, Paul Hudson, had tried and failed to expand the Regeneron alliance, which produced Sanofi's top-selling medicine, Dupixent, among other drugs. "While the assets are early-stage, the expansion should be viewed positively, as it signals the new CEO's proactive focus on the most important yet addressable uncertainties investors face," said Jefferies analyst Michael Leuchten. The four antibody drugs target the same type 2 inflammation pathways as Dupixent and include REGN20423, currently in early-stage testing for atopic dermatitis, an intensely itchy skin condition also known as eczema. The other three are expected to begin clinical testing in 2027. Regeneron will become eligible for the first $1 billion milestone payment when REGN20423 enters late-stage testing, the drugmaker said. Garijo said the atopic dermatitis market could double in the next five years. "We believe today's deal marks an important step in repairing their relationship and removes a key overhang for both," said BMO Capital Markets analyst Evan Seigerman. However, Markus Manns, a portfolio manager at Union Investment, which holds Sanofi shares, questioned the cost, given the uncertainties of such early-stage assets. "Sanofi certainly paid a full price," he said. MORE M&A REQUIRED Analysts broadly viewed the deal positively but some warned it does not solve Sanofi's fundamental challenge of finding enough pipeline strength to offset Dupixent's patent loss later this decade. Dupixent accounted for 36% of Sanofi's nearly 44 billion euros ($49.39 billion) in 2025 sales. It is approved to treat several conditions, including eczema, asthma, nasal polyps and chronic obstructive pulmonary disease. Sanofi said it was actively working to extend Dupixent's patent exclusivity, but declined to provide details. "This (deal) is the necessary first step toward Sanofi regaining investor trust, but a great deal more is required given a decade of R&D challenges," Guggenheim analysts said. ($1 = 0.8909 euros) (Reporting by Hugo Lhomedet and Matthieu Huchet in Gdansk, Bhanvi Satija in London, and Mariam Sunny in Bengaluru, editing by Milla Nissi-Prussak, Louise Heavens and Bill Berkrot)