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Replimune Group Inc.

13.07

-0.3800-2.83%

Post-market: 13.200.1262+0.97%19:54 EDT

Volume:1.30M

Turnover:17.12M

Market Cap:1.23B

PE:-4.14

High:13.83

Open:13.69

Low:12.80

Close:13.45

52wk High:16.33

52wk Low:1.50

Shares:94.22M

Float Shares:77.49M

Volume Ratio:0.48

T/O Rate:1.68%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-3.1550

EPS(LYR):-3.3828

ROE:-134.29%

ROA:-51.30%

PB:11.66

PE(LYR):-3.86

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Overview Company News Filings

Replimune downgraded to Neutral from Overweight at Piper Sandler

Sector Update: Health Care Stocks Lower Friday Afternoon

MT Newswires Live

Replimune CRL positive for Iovance in near-term, says Chardan

Top Midday Decliners

MT Newswires Live

BRIEF-FDA Says Data Insufficient To Conclude Effectiveness Of Replimune's vusolimogene oderparepvec

Replimune Stock Tumbles After FDA Rejects Skin Cancer Therapy for Second Time -- Barrons.com

Replimune's Biologics License Application for Advanced Cutaneous Melanoma Drug Rejected by FDA

MT Newswires Live

Replimune Group's Drug for Advanced Cutaneous Melanoma Rejected by FDA

MT Newswires Live

Replimune issued Complete Response Letter for RP1 for advanced melanoma

FDA, in Complete Response Letter: Data Was Insufficient to Conclude Substantial Evidence of Effectiveness of Replimune's Vusolimogene Oderparepvec

THOMSON REUTERS

US FDA declines to approve Replimune's drug for advanced skin cancer

Replimune sinks after FDA issues complete response letter

Replimune halted for news after dropping 19% to $4.76

Replimune Group trading halted, volatility trading pause

NASDAQ TRADE HALT VOLATILITY TRADING PAUSE AT 10:53 AM

FDA Review Looms As Replimune Faces Weak Technical Setup

Benzinga_recent_news

Replimune Chief Commercial Officer Christopher Sarchi sells USD 52,065 common shares

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The company's biologics license application for vusolimogene oderparepvec to treat unresectable advanced cutaneous melanoma was rejected by the US Food and Drug Administration, the regulator said in a complete response letter.Abbott Laboratories  has been ordered by a jury in Chicago to pay $53 million in compensatory damages to a group of families related to four cases over its infant formula, the Chicago Tribune reported. The families accused the company of allegedly failing to inform them that its infant formula could develop a dangerous intestinal disease in premature infants, the report said. 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CRL positive for Iovance in near-term, says Chardan","url":"https://stock-news.laohu8.com/highlight/detail?id=2626112997","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2626112997?lang=en_us&edition=fundamental","pubTime":"2026-04-11 01:43","pubTimestamp":1775842993,"startTime":"0","endTime":"0","summary":"Chardan analyst Geulah Livshits keeps a Buy rating on Iovance Biotherapeutics (IOVA) with a $16 price target after Replimune (REPL) received a seco...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/replimune-crl-positive-for-iovance-in-near-term-says-chardan-thefly-news?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/the-fly/replimune-crl-positive-for-iovance-in-near-term-says-chardan-thefly-news?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["LU0128526141.USD","IOVA","BK4121","BK4585","CRL","LU0390134368.USD","LU0757428866.USD","BK4588","LU0029874061.USD","LU1815336091.USD","BK4530","IE00BFMHRM44.USD","REPL","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2626114148","title":"Top Midday Decliners","url":"https://stock-news.laohu8.com/highlight/detail?id=2626114148","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2626114148?lang=en_us&edition=fundamental","pubTime":"2026-04-11 01:08","pubTimestamp":1775840913,"startTime":"0","endTime":"0","summary":"One and One Green Technologies  said Friday it signed an agreement with two institutional investors to sell about 1.7 million units in a follow-on offering of its securities at $7.50 per unit, for expected gross proceeds of about $13 million.Shares slid 62%, with intraday trading volume at over 992,000, versus a daily average of roughly 196,000.Angel Studios  said Friday that it priced an underwritten public offering of 14.3 million shares of Class A common stock at $2.10 per share, raising $30 million in expected gross proceeds.Shares sank 26% following an increase in intraday trading volume to over 8.62 million from a daily average of about 762,000.Replimune Group's  biologics license application for vusolimogene oderparepvec was rejected by the US Food and Drug Administration, the regulator said in a complete response letter on Friday.Shares slumped 19% as intraday trading volume soared to more than 2.94 million from a daily average of about 1.75 million.Price: 5.20, Change: -8.71, ","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://www.mtnewswires.com/","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":"mtnewswires_news","symbols":["BK4139","YDDL","REPL","BK4168","BK4108","ANGX"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2626745111","title":"BRIEF-FDA Says Data Insufficient To Conclude Effectiveness Of Replimune's vusolimogene oderparepvec","url":"https://stock-news.laohu8.com/highlight/detail?id=2626745111","media":"Reuters","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2626745111?lang=en_us&edition=fundamental","pubTime":"2026-04-11 00:30","pubTimestamp":1775838642,"startTime":"0","endTime":"0","summary":"BRIEF-FDA Says Data Insufficient To Conclude Effectiveness Of Replimune's vusolimogene oderparepvecApril 10 (Reuters) - FDA:FDA, IN COMPLETE RESPONSE LETTER: DATA WAS INSUFFICIENT TO CONCLUDE SUBSTANT","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:20260410:nFWN40T0PN:1","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":["BK4139","REPL"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2626111521","title":"Replimune Stock Tumbles After FDA Rejects Skin Cancer Therapy for Second Time -- Barrons.com","url":"https://stock-news.laohu8.com/highlight/detail?id=2626111521","media":"Dow Jones","labels":["productRelease","policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2626111521?lang=en_us&edition=fundamental","pubTime":"2026-04-11 00:17","pubTimestamp":1775837820,"startTime":"0","endTime":"0","summary":"Shares of Replimune Group sank on Friday after an application for an experimental skin cancer drug was rejected by the Food and Drug Administration for the second time.The agency declined to approve Replimune's lead investigational immunotherapy, RP1, in combination with Bristol Myers Squibb's Opdivo for the treatment of advanced melanoma.At last check, Replimune shares were down 19% at $4.76, putting the stock on pace for its lowest close since October, according to Dow Jones Market Data. Trading paused twice due to volatility.The FDA rejected an application for the drug in July, two months after Vinay Prasad was appointed to lead the agency's Center for Biologics Evaluation and Research.Regulators said at the time that a clinical trial evaluating the efficacy of RP1 wasn't adequately controlled and failed to provide \"substantial evidence of effectiveness,\" though the FDA raised no safety concerns.Following that setback, Replimune resubmitted its Biologics License Application, which 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Biologics License Application for Advanced Cutaneous Melanoma Drug Rejected by FDA","url":"https://stock-news.laohu8.com/highlight/detail?id=2626118741","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2626118741?lang=en_us&edition=fundamental","pubTime":"2026-04-11 00:00","pubTimestamp":1775836857,"startTime":"0","endTime":"0","summary":"Replimune Group's  biologics license application for vusolimogene oderparepvec was rejected by the US Food and Drug Administration, the regulator said in a complete response letter on Friday.The application was for vusolimogene oderparepvec plus nivolumab to treat adults with unresectable advanced cutaneous melanoma who experienced disease progression with a programmed death receptor-1 blocking antibody-based therapy, the letter said.The regulator and experts unanimously decided that the data presented in the application were \"insufficient\" to show that the treatment is effective for advanced melanoma, the letter added.Shares of Replimune Group were down 19.5% before being halted on Nasdaq at about 11:02 a.m. ET.Price: 4.76, Change: -1.15, Percent Change: -19.46","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.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["IE0031619046.USD","BK4139","LU1815336091.USD","IE00B7SZL793.SGD","IE00B66KJ199.SGD","LU0757428866.USD","BK4585","BK4157","BK4588","LABU","REPL","IE00B19Z4B17.USD","AEIS"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2626611927","title":"Replimune Group's Drug for Advanced Cutaneous Melanoma Rejected by 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-19.46","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://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["AEIS","LU1815336091.USD","LU0757428866.USD","IE0031619046.USD","REPL","BK4139","BK4588","BK4157","LABU","IE00B66KJ199.SGD","IE00B19Z4B17.USD","BK4585","IE00B7SZL793.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2626111871","title":"Replimune issued Complete Response Letter for RP1 for advanced melanoma","url":"https://stock-news.laohu8.com/highlight/detail?id=2626111871","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2626111871?lang=en_us&edition=fundamental","pubTime":"2026-04-10 23:35","pubTimestamp":1775835312,"startTime":"0","endTime":"0","summary":"In a Complete Response Letter addressed to Replimune (REPL) dated April 10 posted to the site of the FDA, the agency stated: “We have completed a 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Chief Commercial Officer Christopher Sarchi sells USD 52,065 common shares","url":"https://stock-news.laohu8.com/highlight/detail?id=2625186601","media":"Reuters","labels":["shareholding","insiderTrades"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2625186601?lang=en_us&edition=fundamental","pubTime":"2026-04-07 04:31","pubTimestamp":1775507478,"startTime":"0","endTime":"0","summary":"Replimune Chief Commercial Officer Christopher Sarchi sold 6,500 shares on April 2, 2026.Sale priced at USD 8.01 per share on weighted-average basis.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 via EDGAR, the Electronic Data Gathering, Analysis, and Retrieval system operated by the U.S. Securities and Exchange Commission , on April 06, 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:20260406:nNDL3k0z2h:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":"Replimune Chief Commercial Officer Christopher Sarchi sells USD 52,065 common shares","news_tag":"shareholding,insiderTrades","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["REPL","BK4139"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":10,"pageCount":10,"totalSize":197,"code":"91000000","status":"200"}]}}