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Replimune Group Inc.

14.58

-0.1950-1.32%

Volume:310.34K

Turnover:4.46M

Market Cap:1.37B

PE:-4.62

High:14.63

Open:14.63

Low:14.11

Close:14.77

52wk High:15.71

52wk Low:1.50

Shares:94.22M

Float Shares:77.49M

Volume Ratio:0.45

T/O Rate:0.40%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-3.1550

EPS(LYR):-3.3828

ROE:-134.29%

ROA:-51.30%

PB:13.00

PE(LYR):-4.31

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Overview Company News Filings

Replimune says RP2 plus nivolumab posts 19.1% response rate in phase 1 advanced solid tumor trial

Replimune Presents Final First-in-Human Data for RP2 in Advanced Solid Tumors During Oral Presentation at the 2026 American Society of Clinical Oncology Annual Meeting

Replimune Group - Rp1 Plus Nivolumab Achieves Median Overall Survival of 32.9 Months in Anti-Pd-1-Failed Melanoma

THOMSON REUTERS

Replimune reports 32.9-month median survival in IGNYTE trial of RP1-nivolumab in anti-PD-1-failed melanoma

Replimune Presents 3-Year Landmark Overall Survival Analysis from IGNYTE Clinical Trial During Oral Presentation at the 2026 American Society of Clinical Oncology Annual Meeting

Top News Today: Stocks Rise as Traders Await Iran Deal Confirmation

Wedbush Adjusts Price Target on Replimune Group to $6 From $2, Maintains Neutral Rating

MT Newswires Live

Top Midday Gainers

MT Newswires Live

Why Penny Stock Replimune (REPL) Nearly Doubled Today

Replimune Shares Soar as FDA Reverses Course on Skin Cancer Drug Application

Replimune Shares Surge 75% After Co Plans to Resubmit US Application for Skin Cancer Drug

THOMSON REUTERS

BUZZ-U.S. STOCKS ON THE MOVE-Tempus AI, SOLV Energy, Replimune

Market Chatter: Replimune Plans to Resubmit Melanoma Therapy Application for FDA Approval

MT Newswires Live

Replimune Gets Third Try at FDA Approval After Makary Departure -- Update

Replimune plans RP1 melanoma BLA resubmission after FDA talks

Replimune reaches agreement with US FDA to resubmit melanoma drug application

Replimune Announces Planned Rp1 Bla Resubmission Following Productive Discussion With FDA

THOMSON REUTERS

Replimune Group - to Resubmit Rp1 Bla for Advanced Melanoma After Alignment With FDA

THOMSON REUTERS

Replimune Group - to Resubmit Rp1 Bla; FDA to Prioritize Review as Urgent

THOMSON REUTERS

BRIEF-Replimune Gets Third Try At FDA Approval After Makary Departure- WSJ

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UMG's board of directors assessed Pershing Square's unsolicited offer and found that it \"fundamentally and materially undervalues UMG and will not deliver superior value creation.\". \"UMG has built an unrivalled position in the music industry through clear vision and execution,\" said board Chairman Sherry Lansing in a statement, adding that the board has \"full confidence\" in Chief Executive Lucian Grainge and his team.Trump Administration Wants Autos Under USMCA to Be at Least 50% Made in America. International Flavors & Fragrances has agreed to sell its food-ingredients business to buyout firm CVC Capital Partners in a deal that values the division at 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The surge followed the company's announcement that it has reached an agreement with the...","market":"sg","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","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":["REPL","BK4588","BK4139","LABU","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2639667897","title":"Replimune Shares Surge 75% After Co Plans to Resubmit US Application for Skin Cancer Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2639667897","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2639667897?lang=en_us&edition=fundamental","pubTime":"2026-05-29 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Chatter: Replimune Plans to Resubmit Melanoma Therapy Application for FDA Approval","url":"https://stock-news.laohu8.com/highlight/detail?id=2639275466","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2639275466?lang=en_us&edition=fundamental","pubTime":"2026-05-29 20:21","pubTimestamp":1780057313,"startTime":"0","endTime":"0","summary":"Replimune (REPL) is planning in the coming days to resubmit a new application with the US Food and Drug Administration for its experimental advanced melanoma treatment, The Wall Street Journal reporte","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://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["LABU","BK4585","BK4588","REPL","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2639627345","title":"Replimune Gets Third Try at FDA Approval After Makary Departure -- Update","url":"https://stock-news.laohu8.com/highlight/detail?id=2639627345","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2639627345?lang=en_us&edition=fundamental","pubTime":"2026-05-29 20:19","pubTimestamp":1780057140,"startTime":"0","endTime":"0","summary":"Replimune Group said Friday it has reached an agreement with the Food and Drug Administration on a path to resubmit its application for its experimental treatment for advanced melanoma.It wasn't immediately clear whether Replimune would submit new clinical data or additional analyses of existing trial results to help secure approval.The company plans to resubmit the application in the coming days, the company said. Replimune shares were up more than 70% in premarket trading.The move marks a sharp reversal for a drug that became one of the most contentious rejections for the agency under the leadership of former FDA Commissioner Marty Makary and illustrates how quickly priorities are shifting in the agency in the wake of the commissioner's departure earlier this month.The FDA twice rejected Replimune's application for approval, first in July 2025 and again in April, saying the data from a single-arm trial, in which all patients received the experimental drug with no comparison group, fe","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":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4588","BK4139","REPL","BK4585","LABU"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2639731622","title":"Replimune plans RP1 melanoma BLA resubmission after FDA talks","url":"https://stock-news.laohu8.com/highlight/detail?id=2639731622","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2639731622?lang=en_us&edition=fundamental","pubTime":"2026-05-29 20:05","pubTimestamp":1780056322,"startTime":"0","endTime":"0","summary":"Replimune plans to resubmit its RP1 biologics license application for advanced melanoma in the coming days following FDA discussions.The FDA signaled it will treat the resubmission as urgent and prioritize the review once received.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Replimune Group Inc. published the original content used to generate this news brief on May 29, 2026, and is solely responsible for the information contained therein.","market":"fut","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:20260529:nNDL3cHcNm: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":null,"symbols":["REPL","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2639234622","title":"Replimune reaches agreement with US FDA to resubmit melanoma drug application","url":"https://stock-news.laohu8.com/highlight/detail?id=2639234622","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2639234622?lang=en_us&edition=fundamental","pubTime":"2026-05-29 20:03","pubTimestamp":1780056220,"startTime":"0","endTime":"0","summary":"Replimune reaches agreement with US FDA to resubmit melanoma drug applicationMay 29  - Replimune REPL.O said on Friday it it has reached an agreement with the U.S. Food and Drug Administration to resubmit the marketing application for its experimental skin cancer drug after the regulator twice declined to approve the therapy.  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