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Regeneron Pharmaceuticals

798.58

+4.390.55%

Volume:236.04K

Turnover:187.41M

Market Cap:82.22B

PE:19.75

High:799.51

Open:782.44

Low:779.08

Close:794.19

52wk High:847.00

52wk Low:541.00

Shares:102.95M

Float Shares:98.88M

Volume Ratio:0.41

T/O Rate:0.24%

Dividend:3.64

Dividend Rate:0.46%

EPS(TTM):40.43

EPS(LYR):41.48

ROE:14.04%

ROA:6.53%

PB:2.59

PE(LYR):19.25

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Overview Company News Filings

Market Chatter: Eli Lilly, Regeneron Among First Companies in FDA PreCheck Pilot Program

MT Newswires Live

Lilly, Regeneron Selected for US Program to Review New Manufacturing Plants Faster

Eli Lilly, Regeneron among first selections for FDA PreCheck program, CNBC says

Eli Lilly, Regeneron Among First Companies Selected for FDA Initiative to Speed Review of New Manufacturing Facilities - CNBC

THOMSON REUTERS

Healthcare Stocks Have Become a Haven for Investors Ditching Tech

Regeneron Pharmaceuticals Inc. Stock Outperforms Competitors on Strong Trading Day

How Investors May Respond To Regeneron Pharmaceuticals (REGN) Cemdisiran Priority Review for gMG Treatment

Simply Wall St.

Regeneron Updates Financial Calendar for Second-quarter Results Release and Conference Call

Regeneron’s New First-in-Human Eczema Drug REGN20423: Early Trial Progress and Investor Takeaways

Kymera Rises on Accelerated Trial Timeline for Experimental Eczema Drug

AbbVie is buying a biotech working on an experimental eczema drug for $10.9 billion

Regeneron Gets FDA, EMA Review of Cemdisiran in Generalized Myasthenia Gravis

Regeneron says FDA accepts cemdisiran gMG filing for priority review

Regeneron Pharmaceuticals - FDA to Review Cemdisiran Nda Under Priority Review With Target Action Date November 2026

THOMSON REUTERS

Regeneron Pharmaceuticals - European Commission Decision on Cemdisiran Expected in Second Half of 2027

THOMSON REUTERS

Cemdisiran Regulatory Submissions Accepted for Review by FDA and Ema for the Treatment of Generalized Myasthenia Gravis (Gmg)

THOMSON REUTERS

Regeneron Pharmaceuticals - Plans Regulatory Filing for Cemdisiran in Japan in Early 2027

THOMSON REUTERS

Cemdisiran Regulatory Submissions Accepted for Review by FDA and EMA for the Treatment of Generalized Myasthenia Gravis (gMG)

AbbVie would gain an experimental eczema drug by buying biotech: report

Regeneron Pharmaceuticals Inc. Stock Outperforms Competitors Despite Losses On The Day

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Chatter: Eli Lilly, Regeneron Among First Companies in FDA PreCheck Pilot Program","url":"https://stock-news.laohu8.com/highlight/detail?id=2647304917","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2647304917?lang=en_us&edition=fundamental","pubTime":"2026-06-30 04:00","pubTimestamp":1782763235,"startTime":"0","endTime":"0","summary":"Eli Lilly  and Regeneron Pharmaceuticals  are among the first seven companies selected by the U.S. Food and Drug Administration for a pilot program aimed at accelerating reviews of new domestic manufacturing facilities, CNBC reported Monday, citing FDA spokesperson Benjamin Nichols.The other participants in the FDA's PreCheck pilot program are Amneal Pharmaceuticals , Cellares, Fujifilm Biotechnologies, Kriya Therapeutics and Kyowa Kirin, the report said.The program allows regulators to begin reviewing new manufacturing facilities while they are still under construction, which the agency estimates could save companies up to 14 months, according to the report.Eli Lilly, Regeneron and FDA did not immediately respond to requests for comment from MT Newswires.Price: 1228.24, Change: +20.12, Percent Change: 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Stock Outperforms Competitors On Strong Trading DayThis article was automatically generated by MarketWatch using technology from Automated Insights.Shares of Regeneron Pharmaceuticals Inc.  rallied 2.06% to $632.90 Friday, on what proved to be an all-around dismal trading session for the stock market, with the S&P 500 Index  falling 0.05% to 7,354.02 and Dow Jones Industrial Average  falling 0.09% to 51,876.11.Regeneron Pharmaceuticals Inc. closed 22.92% short of its 52-week high of $821.11, which the company reached on January 9th.The stock demonstrated a mixed performance when compared to some of its competitors Friday, as Amgen Inc.  rose 1.56% to $358.33, Moderna Inc.  rose 12.59% to $67.27, and Gilead Sciences Inc.  rose 3.26% to $127.88.Trading volume  eclipsed its 50-day average volume of 1.0 M.Data source: Dow Jones Market Data, FactSet. Data compiled June 26, 2026.This content was created by MarketWatch, which is operated by Dow Jones & Co. 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New First-in-Human Eczema Drug REGN20423: Early Trial Progress and Investor Takeaways","url":"https://stock-news.laohu8.com/highlight/detail?id=2646802032","media":"TIPRANKS","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2646802032?lang=en_us&edition=fundamental","pubTime":"2026-06-26 00:31","pubTimestamp":1782405089,"startTime":"0","endTime":"0","summary":"Regeneron Pharmaceuticals ($REGN) announced an update on their ongoing clinical study. Regeneron Pharmaceuticals, Inc. 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AbbVie is buying Apogee Therapeutics, which is developing a long-acting treatment for atopic dermatitis.AbbVie is acquiring a biotech company that is developing a promising atopic dermatitis drug for $10.9 billion in cash.The acquisition would be for Apogee Therapeutics, which is working on a long-acting treatment for atopic dermatitis that's set to move into Phase 3 trials later this year. The drug works by blocking IL-13, the protein that causes eczema.If approved, the drug would compete with Dupixent, an IL-4 and IL-13 inhibitor that is used to treat numerous inflammatory conditions like atopic dermatitis and chronic obstructive pulmonary disease, or COPD. That medicine, which is sold by Regeneron Pharmaceuticals  and Sanofi , is one of the world's top-selling drugs.This content was created by MarketWatch, which is operated by Dow Jones & Co. MarketWatch is published independently from Dow 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Gets FDA, EMA Review of Cemdisiran in Generalized Myasthenia Gravis","url":"https://stock-news.laohu8.com/highlight/detail?id=2645141021","media":"Dow Jones","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2645141021?lang=en_us&edition=fundamental","pubTime":"2026-06-22 19:33","pubTimestamp":1782127980,"startTime":"0","endTime":"0","summary":"Regeneron Pharmaceuticals said U.S. and European regulators have accepted its applications seeking approval of its cemdisiran drug candidate in the rare and chronic autoimmune disease generalized myasthenia gravis, or gMG.Regeneron on Monday said the U.S. Food and Drug Administration and the European Medicines Agency will review cemdisiran to for adults with gMG who are anti-acetylcholine receptor antibody-positive.The Tarrytown, N.Y., biotechnology company said the FDA has granted the application priority review, which shortens the review period, and that it set a target action date in November.Regeneron, which is developing cemdisiran under a licensing agreement with Alnylam Pharmaceuticals, said it expects a decision from the European Commission in the second half of 2027.","market":"sg","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0058720904.USD","LU1974910355.USD","BK4588","LU0114720955.EUR","LU2362541273.HKD","LU0109394709.USD","LU2468319806.SGD","BK4139","LU2089984988.USD","LU1917777945.USD","LU0823434740.USD","LU2106854487.HKD","LU0889565916.HKD","BK4081","LU2362541513.USD","LU2362540622.SGD","LU0320765992.SGD","EMA","BK4548","BK4585","ALNY","LU2237438978.USD","LU0823416689.USD","LU0882574055.USD","LU2023250504.SGD","LU0053666078.USD","LU0823434583.USD","LABU","LU0289739699.SGD","REGN"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2645029935","title":"Regeneron says FDA accepts cemdisiran gMG filing for priority review","url":"https://stock-news.laohu8.com/highlight/detail?id=2645029935","media":"Reuters","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2645029935?lang=en_us&edition=fundamental","pubTime":"2026-06-22 19:00","pubTimestamp":1782126059,"startTime":"0","endTime":"0","summary":"Regeneron’s FDA application for cemdisiran in anti-AChR antibody-positive generalized myasthenia gravis was accepted under Priority Review.FDA target action date set for November 2026, supported by a Priority Review Voucher.EMA also validated the filing; a European Commission decision is expected in the second half of 2027.","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260622:nNDL9dkh2n:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0889565916.HKD","LU1917777945.USD","LU2210149790.SGD","LU2468319806.SGD","LU2089984988.USD","LU0823434740.USD","SG9999014005.SGD","IE00BKPKM429.USD","BK4588","LU1974910355.USD","LU0314104364.USD","LU0823434583.USD","LU0289739699.SGD","LU0109394709.USD","LU2095319765.USD","LU2023250504.SGD","BK4585","BK4139","LU0053666078.USD","LU2106854487.HKD","IE00BN0W2V16.EUR","LU0058720904.USD","LU2362541273.HKD","LU2362541513.USD","LU2210150020.SGD","NDAQ","SG9999014013.SGD","IE00B3QW5Z07.USD","LU0114720955.EUR","LU2362540622.SGD","BK4112","IE00BN0W2W23.USD","SG9999014039.USD","REGN","LU2237438978.USD","LU0320765992.SGD","LU0823416689.USD","LU0882574055.USD","IE00BGHQF748.EUR","SG9999014021.USD","IE00BN0W2T93.GBP","IE00B64PRP62.GBP"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2645951029","title":"Regeneron Pharmaceuticals - FDA to Review Cemdisiran Nda Under Priority Review With Target Action Date November 2026","url":"https://stock-news.laohu8.com/highlight/detail?id=2645951029","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2645951029?lang=en_us&edition=fundamental","pubTime":"2026-06-22 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Pharmaceuticals - European Commission Decision on Cemdisiran Expected in Second Half of 2027","url":"https://stock-news.laohu8.com/highlight/detail?id=2645802995","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2645802995?lang=en_us&edition=fundamental","pubTime":"2026-06-22 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Regulatory Submissions Accepted for Review by FDA and Ema for the Treatment of Generalized Myasthenia Gravis (Gmg)","url":"https://stock-news.laohu8.com/highlight/detail?id=2645622029","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2645622029?lang=en_us&edition=fundamental","pubTime":"2026-06-22 19:00","pubTimestamp":1782126001,"startTime":"0","endTime":"0","summary":null,"market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260622:nTUA2BRBYY:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"reuters_en_live","symbols":["LU0289739699.SGD","LU2468319806.SGD","LU0114720955.EUR","LU0823434583.USD","LU0320765992.SGD","LU0109394709.USD","LU2362541273.HKD","BK4585","LU2362540622.SGD","LU0823434740.USD","LU0823416689.USD","BK4139","REGN","BK4588","LU0058720904.USD","LU2362541513.USD","LU1974910355.USD","LU2023250504.SGD","LU0882574055.USD","LU0053666078.USD","LU2106854487.HKD","LU2089984988.USD","LU0889565916.HKD","LU1917777945.USD","LU2237438978.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2645029952","title":"Regeneron Pharmaceuticals - Plans Regulatory Filing for Cemdisiran in Japan in Early 2027","url":"https://stock-news.laohu8.com/highlight/detail?id=2645029952","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2645029952?lang=en_us&edition=fundamental","pubTime":"2026-06-22 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Regulatory Submissions Accepted for Review by FDA and EMA for the Treatment of Generalized Myasthenia Gravis (gMG)","url":"https://stock-news.laohu8.com/highlight/detail?id=2645021109","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2645021109?lang=en_us&edition=fundamental","pubTime":"2026-06-22 19:00","pubTimestamp":1782126000,"startTime":"0","endTime":"0","summary":"Cemdisiran could be the first siRNA approved for the treatment of gMG and only therapy to be offered subcutaneously with four times a year dosing FDA accepted NDA under Priority Review with a target a","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.globenewswire.com/news-release/2026/06/22/3315167/0/en/Cemdisiran-Regulatory-Submissions-Accepted-for-Review-by-FDA-and-EMA-for-the-Treatment-of-Generalized-Myasthenia-Gravis-gMG.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0320765992.SGD","EMA","LU1974910355.USD","LU2089984988.USD","LU0109394709.USD","BK4139","LU2106854487.HKD","LU0058720904.USD","LU0823416689.USD","LU0823434740.USD","LU2362541273.HKD","LABU","LU0889565916.HKD","LU1917777945.USD","LU2023250504.SGD","LU0882574055.USD","LU2362541513.USD","BK4585","BK4588","LU0053666078.USD","LU2237438978.USD","REGN","LU0289739699.SGD","LU0823434583.USD","LU0114720955.EUR","LU2362540622.SGD","LU2468319806.SGD","BK4081"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2645409366","title":"AbbVie would gain an experimental eczema drug by buying biotech: report","url":"https://stock-news.laohu8.com/highlight/detail?id=2645409366","media":"Dow Jones","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2645409366?lang=en_us&edition=fundamental","pubTime":"2026-06-21 00:11","pubTimestamp":1781971860,"startTime":"0","endTime":"0","summary":"If approved, the drug would be a new option for people with atopic dermatitis. AbbVie is reportedly nearing a deal to buy Apogee Therapeutics, which is developing a long-acting treatment for atopic dermatitis.AbbVie is reportedly trying to buy a biotech company that is developing a promising atopic dermatitis drug for $10.9 billion in cash, according to a Financial Times report.The acquisition would be for Apogee Therapeutics , which is working on a long-acting treatment for atopic dermatitis that's set to move into Phase 3 trials later this year. The drug works by blocking IL-13, the protein that causes eczema.If approved, the drug would compete with Dupixent, an IL-4 and IL-13 inhibitor that is used to treat numerous inflammatory conditions like atopic dermatitis and chronic obstructive pulmonary disease, or COPD. That medicine, which is sold by Regeneron Pharmaceuticals  and Sanofi , is one of the world's top-selling drugs.This content was created by MarketWatch, which is operated b","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0456855351.SGD","LU0912757837.SGD","IE00BGHQF631.EUR","LU1093756168.USD","IE00B19Z3581.USD","LU2129689431.USD","LU1934455194.USD","LU1934455277.USD","LU1585245621.USD","LU2237438978.USD","SG9999015945.SGD","LU2023250504.SGD","LU0098860793.USD","IE000BZT7R73.USD","IE00BDGV0183.EUR","SG9999015978.USD","LU0289961442.SGD","LU1244550494.USD","LU1670628061.USD","SG9999015986.USD","LU1551013425.SGD","LU0069063385.USD","LU1093756325.SGD","LU2347655156.SGD","LU2237443978.SGD","ABBV","LU0689626769.HKD","LU0859254822.USD","IE00B2B36J28.USD","LU0965508806.USD","REGN","IE00BJT1NW94.SGD","LU0949170772.SGD","LU2133065610.SGD","LU1974910355.USD","LU1037948897.HKD","LU1430594728.SGD","IE00B19Z3B42.SGD","LU1839511570.USD","LU0889565916.HKD","LU2362540622.SGD","LU1291159041.SGD","APGE","SG9999015952.SGD","LU0211328371.USD","LU0053666078.USD","LU1267930490.SGD","LU0432979614.USD","LU0109394709.USD","IE0000B7K699.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2644721050","title":"Regeneron Pharmaceuticals Inc. Stock Outperforms Competitors Despite Losses On The Day","url":"https://stock-news.laohu8.com/highlight/detail?id=2644721050","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2644721050?lang=en_us&edition=fundamental","pubTime":"2026-06-18 04:46","pubTimestamp":1781729160,"startTime":"0","endTime":"0","summary":"This article was automatically generated by MarketWatch using technology from Automated Insights.Shares of Regeneron Pharmaceuticals Inc.  shed 1.11% to $607.93 Wednesday, on what proved to be an all-around dismal trading session for the stock market, with the S&P 500 Index  falling 1.21% to 7,420.10 and Dow Jones Industrial Average  falling 0.98% to 51,492.55.This was the stock's second consecutive day of losses.Regeneron Pharmaceuticals Inc. closed 25.96% short of its 52-week high of $821.11, which the company reached on January 9th.The stock demonstrated a mixed performance when compared to some of its competitors Wednesday, as Amgen Inc.  fell 1.78% to $341.66, Moderna Inc.  rose 11.55% to $61.80, and Gilead Sciences Inc.  fell 1.40% to $125.45.Trading volume  eclipsed its 50-day average volume of 955,366.Data source: Dow Jones Market Data, FactSet. Data compiled June 17, 2026.This content was created by MarketWatch, which is operated by Dow Jones & Co. MarketWatch is published ind","market":"sg","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":["rate"],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["REGN"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":10,"pageCount":8,"totalSize":200,"code":"91000000","status":"200"}]}}