Regeneron Earnings: Raising Our Fair Value on Near-Term Eylea Boost, Long-Term Dupixent Prospects

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Regeneron Pharmaceuticals Inc
(REGN)

We’re raising our Regeneron REGN fair value estimate to $750 from $690 following solid second-quarter performance, particularly as we think Dupixent’s long-term prospects continue to improve and Eylea sales stay steadier than we anticipated, in the face of branded competition from Roche’s Vabysmo. Regeneron’s revenue grew 11% in the second quarter as continued stellar growth for immunology drug Dupixent (33%) drove collaboration revenue from partner Sanofi to grow by an even higher 39% as Dupixent’s profitability improves. This countered some weakness in ophthalmology drug Eylea due to price concessions in the face of the launch of Vabysmo. We assume that upcoming approvals for Dupixent will only add to the drug’s blockbuster sales, driving peak sales approaching $20 billion in 2029 (ahead of potential Medicare negotiation). We expect COPD approval in 2025, with potential approval of COPD antibody itepekimab in 2026 to complement Dupixent. Overall, we think Regeneron’s core antibody Dupixent as well as a growing oncology pipeline support a narrow moat, regardless of whether Eylea can continue to grow as the high-dose version launches later this year.

We still expect Vabysmo and high-dose Eylea to share the market relatively equally in the long run, with both drugs likely to generate at least $5 billion in annual sales. While Vabysmo has been taking share from Eylea and driving U.S. sales declines since the fourth quarter of 2022, Regeneron expects a potential third-quarter approval of high-dose Eylea, as its contract manufacturer Catalent is submitting additional information to the Food and Drug Administration in mid-August to address a complete response letter (tied to manufacturing) received in June. We note that the entire market for degenerative eye disease drugs like Eylea and Vabysmo has been growing at a double-digit level, evidence that the Vabysmo launch is expanding the market.

The author or authors do not own shares in any securities mentioned in this article. Find out about Morningstar’s editorial policies.

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Karen Andersen, CFA

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Karen Andersen, CFA, is a sector director, AM Healthcare, for Morningstar*. In addition to leading the sector team, she covers biopharma firms in the US and Europe, focusing mostly on large-cap firms with foundations in biologic or gene-based medicines.

Before joining Morningstar in 2005, Andersen received a master’s degree in business administration from the Jones Graduate School of Business at Rice University, where she served as senior healthcare analyst for the M.A. Wright Fund and earned the distinction of Jones Scholar. She also holds the Chartered Financial Analyst® designation.

She ranked first in the biotechnology industry, and had the highest score overall, in The Wall Street Journal’s annual “Best on the Street” analysts survey in 2013, the last year the survey was conducted.

Andersen holds a bachelor’s degree in biochemistry from Rice University, where she graduated magna cum laude. She is also a member of Phi Beta Kappa. She has scientific research experience in academia at both Rice University and the University of Queensland in Australia. She also worked in the healthcare industry, both at genetic testing firm Integrated Genetics (now part of LabCorp) and as a research assistant at Lexicon Genetics (now Lexicon Pharmaceuticals).

* Morningstar Research Services LLC (“Morningstar”) is a wholly owned subsidiary of Morningstar, Inc

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