Replimune Group, Inc. (REPL)

US — Healthcare Sector
Peers: PCVX  LRMR  SNDX  MRUS  STRO  CRNX  SRRK  YMAB  STOK 

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Key Metrics & Ratings

  • symbol REPL
  • Rev/Share 0.0161
  • Book/Share 3.6793
  • PB 1.641
  • Debt/Equity 0.2267
  • CurrentRatio 6.9399
  • ROIC -0.7109

 

  • MktCap 471285913.0
  • FreeCF/Share -2.4898
  • PFCF -2.0683
  • PE -1.9719
  • Debt/Assets 0.1626
  • DivYield 0
  • ROE -0.6934

 

  • Rating C
  • Score 2
  • Recommendation Sell
  • P/E Score 1
  • DCF Score 3
  • P/B Score 3
  • D/E Score 2

Recent Analyst Ratings

Type Ticker Analyst Firm Previous Rating Current Rating Previous Price Target Current Price Target Date
Upgrade REPL Cantor Fitzgerald Neutral Overweight -- -- July 30, 2025
Downgrade REPL H.C. Wainwright Buy Neutral -- -- July 23, 2025
Downgrade REPL BMO Capital Markets Outperform Underperform -- $2 July 23, 2025
Downgrade REPL Barclays Overweight Equal Weight -- $3 July 23, 2025
Downgrade REPL Wedbush Outperform Neutral -- $4 July 22, 2025
Downgrade REPL JP Morgan Overweight Neutral -- $9 July 22, 2025
Downgrade REPL Leerink Partners Outperform Market Perform -- $3 July 22, 2025
Downgrade REPL Piper Sandler Overweight Neutral -- $3 July 22, 2025
Initiation REPL Cantor Fitzgerald -- Overweight -- -- June 20, 2025
Initiation REPL ROTH MKM -- Buy -- $17 Aug. 28, 2024

News

INVESTOR ALERT: Class Action Lawsuit Filed on Behalf of Replimune Group (REPL) Investors – Holzer & Holzer, LLC Encourages Investors With Significant Losses to Contact the Firm
REPL
Published: July 25, 2025 by: GlobeNewsWire
Sentiment: Neutral

ATLANTA, July 25, 2025 (GLOBE NEWSWIRE) -- A shareholder class action lawsuit has been filed against Replimune Group, Inc. (“Replimune” or the “Company”) (NASDAQ: REPL). The lawsuit alleges that Defendants made materially false and/or misleading statements and/or failed to disclose material adverse information, including allegations that: (1) Defendants recklessly overstated the IGNYTE trial's prospects, given material issues that defendants knew or should have known of, which resulted in the FDA deeming the IGNYTE trial inadequate and not well-controlled; and (2) as a result, defendants' statements about Replimune's business, operations, and prospects were materially false and misleading and/or lacked a reasonable …

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image for news INVESTOR ALERT: Class Action Lawsuit Filed on Behalf of Replimune Group (REPL) Investors – Holzer & Holzer, LLC Encourages Investors With Significant Losses to Contact the Firm
Replimune Group, Inc. Investors: Company Investigated by the Portnoy Law Firm
REPL
Published: July 24, 2025 by: GlobeNewsWire
Sentiment: Neutral

Investors can contact the law firm at no cost to learn more about recovering their losses

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image for news Replimune Group, Inc. Investors: Company Investigated by the Portnoy Law Firm
INVESTOR ALERT: Investigation of Replimune Group, Inc. (REPL) Announced by Holzer & Holzer, LLC
REPL
Published: July 24, 2025 by: GlobeNewsWire
Sentiment: Neutral

ATLANTA, July 24, 2025 (GLOBE NEWSWIRE) -- Holzer & Holzer, LLC is investigating whether Replimune Group, Inc. (“Replimune” or the “Company”) (NASDAQ: REPL) complied with federal securities laws. On July 22, 2025, Replimune announced it received a Complete Response Letter (“CRL”) from the FDA regarding the Biologics License Application (“BLA”) for RP1 (vusolimogene oderparepvec) in combination with nivolumab for the treatment of advanced melanoma. In the CRL, the FDA indicated “that the IGNYTE trial is not considered to be an adequate and well-controlled clinical investigation that provides substantial evidence of effectiveness.” Following this news, the price of the Company's stock …

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image for news INVESTOR ALERT: Investigation of Replimune Group, Inc. (REPL) Announced by Holzer & Holzer, LLC
INVESTOR ALERT: Investigation of Replimune Group, Inc. (REPL) Announced by Holzer & Holzer, LLC
REPL
Published: July 22, 2025 by: GlobeNewsWire
Sentiment: Neutral

ATLANTA, July 22, 2025 (GLOBE NEWSWIRE) -- Holzer & Holzer, LLC is investigating whether Replimune Group, Inc. (“Replimune” or the “Company”) (NASDAQ: REPL) complied with federal securities laws. On July 22, 2025, Replimune announced it received a Complete Response Letter (“CRL”) from the FDA regarding the Biologics License Application (“BLA”) for RP1 (vusolimogene oderparepvec) in combination with nivolumab for the treatment of advanced melanoma. In the CRL, the FDA indicated “that the IGNYTE trial is not considered to be an adequate and well-controlled clinical investigation that provides substantial evidence of effectiveness.” Following this news, the price of the Company's stock …

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image for news INVESTOR ALERT: Investigation of Replimune Group, Inc. (REPL) Announced by Holzer & Holzer, LLC
BREAKING: Replimune Group, Inc. Shares Drop 70%; Securities Fraud Investigation by Block & Leviton Could Allow Investors to Recover Losses
REPL
Published: July 22, 2025 by: GlobeNewsWire
Sentiment: Neutral

BOSTON, July 22, 2025 (GLOBE NEWSWIRE) -- Block & Leviton LLP is investigating Replimune Group, Inc. (Nasdaq: REPL) for potential securities law violations. Investors who have lost money in their Replimune Group, Inc. investment should contact the firm to learn more about how they might recover those losses.

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image for news BREAKING: Replimune Group, Inc. Shares Drop 70%; Securities Fraud Investigation by Block & Leviton Could Allow Investors to Recover Losses
Replimune Group, Inc. (REPL) Q4 2025 Earnings Call Transcript
REPL
Published: May 22, 2025 by: Seeking Alpha
Sentiment: Neutral

Replimune Group, Inc. (NASDAQ:REPL ) Q4 2025 Results Conference Call May 22, 2025 8:00 AM ET Company Participants Arleen Goldenberg - Senior Communications Leader Sushil Patel - Chief Executive Officer Chris Sarchi - Chief Commercial Officer Emily Hill - Chief Financial Officer Conference Call Participants Anupam Rama - J.P. Morgan Roger Song - Jefferies Jonathan Chang - Leerink Allison Bratzel - Piper Sandler Peter Lawson - Barclays Operator Good morning and welcome to the Replimune Fiscal Year Fourth Quarter 2025 Financial Results and Corporate Update Conference Call.

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image for news Replimune Group, Inc. (REPL) Q4 2025 Earnings Call Transcript
Replimune Reports Fiscal Fourth Quarter and Year End 2025 Financial Results and Provides Corporate Update
REPL
Published: May 22, 2025 by: GlobeNewsWire
Sentiment: Neutral

• BLA priority review of RP1 plus nivolumab in advanced melanoma proceeding on schedule; manufacturing inspections and late cycle review meeting complete • Full commercial infrastructure for launch in place ahead of July 22nd PDUFA date • Conference call today at 8:00 AM ET WOBURN, Mass., May 22, 2025 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (Nasdaq: REPL), a clinical stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced financial results for the fiscal fourth quarter and year ended March 31, 2025 and provided a business update.

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image for news Replimune Reports Fiscal Fourth Quarter and Year End 2025 Financial Results and Provides Corporate Update
Replimune Announces Dates for Fiscal Fourth Quarter and Year End 2025 Financial Results and Upcoming Investor Day
REPL
Published: May 16, 2025 by: GlobeNewsWire
Sentiment: Neutral

WOBURN, Mass., May 16, 2025 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced that it will host a conference call on Thursday, May 22, 2025 at 8:00 a.m. ET to discuss its financial results for the fiscal fourth quarter and year end March 31, 2025. Additionally, the Company will host an Investor Day on Tuesday, June 24, 2025.

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image for news Replimune Announces Dates for Fiscal Fourth Quarter and Year End 2025 Financial Results and Upcoming Investor Day
Sibylla Biotech Appoints Former Bayer CEO, Dieter Weinand, as Chairman of the Board of Directors
COYA, REPL
Published: May 08, 2025 by: GlobeNewsWire
Sentiment: Neutral

Milan, Italy, May 8, 2025 – Sibylla Biotech today announced the appointment of Dieter Weinand as Chairman of its Board of Directors. Mr. Weinand is an industry veteran, boasting over 35 years in the pharmaceutical sector, including leading business units and drug commercialization initiatives at global organizations. His background includes serving as President, CEO and Chairman of the Board of Bayer Pharmaceuticals AG. At Sibylla, Mr. Weinand's profound knowledge will guide the Board as the company advances its innovative Pharmacological Protein Inactivation by Folding Intermediates Targeting (PPI-FIT) technology and pipeline of folding interference small molecules to address a range of …

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image for news Sibylla Biotech Appoints Former Bayer CEO, Dieter Weinand, as Chairman of the Board of Directors
Replimune Reports Fiscal Third Quarter 2025 Financial Results and Provides Corporate Update
REPL
Published: February 12, 2025 by: GlobeNewsWire
Sentiment: Neutral

U.S. Food and Drug Administration (FDA) recently accepted the Biologics License Application (BLA) for RP1 plus nivolumab in advanced melanoma for priority review with a PDUFA date of July 22, 2025 IGNYTE-3 confirmatory trial of RP1(vusolimogene oderparepvec) plus nivolumab in advanced melanoma is enrolling Enrolled first patients in trials evaluating RP2 for the treatment of metastatic uveal melanoma and hepatocellular carcinoma WOBURN, Mass., Feb. 12, 2025 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (Nasdaq: REPL), a clinical stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced financial results for the fiscal third quarter ended December 31, 2024 and …

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image for news Replimune Reports Fiscal Third Quarter 2025 Financial Results and Provides Corporate Update

About Replimune Group, Inc. (REPL)

  • IPO Date 2018-07-20
  • Website https://www.replimune.com
  • Industry Biotechnology
  • CEO Sushil Patel
  • Employees 479

Replimune Group, Inc., a biotechnology company, develops oncolytic immuno-gene therapies to treat cancer. It uses its proprietary Immunotherapy platform to design and develop product candidates that are intended to activate the immune system against cancer. The company's lead product candidate is RP1, a selectively replicating version of herpes simplex virus 1, which is in Phase I/II clinical trials for a range of solid tumors; and that is in Phase II clinical trials for patients with cutaneous squamous cell carcinoma. It is also developing RP2, which is in Phase I clinical trials for an anti-CTLA-4 antibody-like protein in order to block the inhibition of the immune response otherwise caused by CTLA-4; and RP3 that is in Phase I clinical trials to express immune-activating proteins that stimulate T cells. Replimune Group, Inc. was founded in 2015 and is headquartered in Woburn, Massachusetts.