NASDAQ : REPL

Replimune Group, Inc. — News

$11.2 USD

$5.79 (107.02%)

Volume
33.34M
Average Volume
5.94M
Market Capitalization
$940.4M
P/E Ratio
-3.31
Dividend Yield
0.00%
Price Target
$14.00
Year High
$12.50
Year Low
$1.50
Day High
Day Low
Payout Ratio
$0.00
Current Ratio
$4.79
Source Headline
Securities Fraud Investigation Into Replimune Group Inc. (REPL) Continues – Shareholders Who Lost Money Urged To Contact Glancy Prongay Wolke & Rotter LLP, a Leading Securities Fraud Law Firm

LOS ANGELES, July 31, 2026 (GLOBE NEWSWIRE) -- Glancy Prongay Wolke & Rotter LLP, a leading national shareholder rights law firm, continues its investigation on behalf of Replimune Group Inc. (“Replimune” or the “Company”) (NASDAQ: REPL) investors concerning the Company's possible violations of the federal securities laws.

globenewswire.com - 2026-07-31 11:00:00

Replimune Skin Cancer Therapy Hopes Revive After Positive FDA Panel Vote

Replimune Group Inc. (NASDAQ:REPL) stock more than doubled on Friday after the U.S. Food and Drug Administration's (FDA) Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) voted in favor of the company's IGNYTE study data.

benzinga.com - 2026-07-31 10:09:17

Replimune surges after FDA advisers back skin cancer drug

Shares ‌of Replimune more than doubled premarket on Friday after the U.S. Food and Drug Administration's panel of outside advisers voted to back trial results for its drug for a ​type of skin cancer.

reuters.com - 2026-07-31 05:40:30

Replimune Announces Favorable Outcome of FDA's Cellular, Tissue, and Gene Therapies Advisory Committee Meeting for RP1 in Advanced Melanoma

WOBURN, Mass., July 30, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (Nasdaq: REPL), a clinical-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced the outcome of today's meeting of the U.S. Food and Drug Administration's (FDA) Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC), which discussed the Biologics License Application (BLA) resubmission for RP1 (vusolimogene oderparepvec) in combination with nivolumab for the treatment of advanced melanoma in patients who have progressed on prior anti-PD-1 therapy.

globenewswire.com - 2026-07-30 18:15:00

Bragar Eagel & Squire, P.C. is Investigating Replimune Group Inc. on Behalf of Replimune Stockholders and Encourages Investors to Contact the Firm

Bragar Eagel & Squire, P.C.  Litigation Partner  Brandon Walker  Encourages Investors Who Suffered Losses In Replimune (REPL) To Contact Him Directly To Discuss Their Options

globenewswire.com - 2026-07-30 17:48:00

A Food and Drug Administration advisory panel voted 10-3 for Replimune Group's experimental melanoma therapy, after experts raised doubts about whether the company's data and trial design could be trusted to show the drug works

Independent experts voted 10-3 despite regulators' concern about the design of the company's pivotal cancer trial.

wsj.com - 2026-07-30 17:27:00

US FDA panel backs Replimune skin cancer drug study data

A panel of outside ​advisers to the US Food ‌and Drug Administration voted to back results from a trial ​studying Replimune's drug for ​a type of skin cancer ⁠in a meeting on ​Thursday.

reuters.com - 2026-07-30 17:10:52

INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Replimune Group, Inc. - REPL

NEW YORK, July 30, 2026 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Replimune Group, Inc. ("Replimune" or the "Company") (NASDAQ: REPL). Such investors are advised to contact Danielle Peyton at [email protected] or 646-581-9980, ext.

prnewswire.com - 2026-07-30 10:00:00

REPL INVESTOR ALERT: Kirby McInerney LLP Announces Investigation Into Potential Securities Fraud

NEW YORK, July 29, 2026 (GLOBE NEWSWIRE) -- The law firm of Kirby McInerney LLP is investigating potential claims against Replimune Group Inc. (“Replimune” or the “Company”) (NASDAQ: REPL). The investigation concerns whether the Company and/or members of its senior management may have violated federal securities laws or engaged in other unlawful business practices.

globenewswire.com - 2026-07-29 20:00:00

Securities Fraud Investigation Into Replimune Group Inc. (REPL) Announced – Shareholders Who Lost Money Urged To Contact Glancy Prongay Wolke & Rotter LLP, a Leading Securities Fraud Law Firm

LOS ANGELES--(BUSINESS WIRE)--Glancy Prongay Wolke & Rotter LLP, a leading national shareholder rights law firm, today announced that it has commenced an investigation on behalf of Replimune Group Inc. (“Replimune” or the “Company”) (NASDAQ: REPL) investors concerning the Company's possible violations of the federal securities laws. IF YOU ARE AN INVESTOR WHO LOST MONEY ON REPLIMUNE GROUP INC. (REPL) CLICK HERE TO INQUIRE ABOUT POTENTIALLY PURSUING CLAIMS TO RECOVER YOUR LOSS. What Happened.

businesswire.com - 2026-07-29 15:12:00

Replimune Group Inc. (REPL) Shareholders Who Lost Money – Contact Law Offices of Howard G. Smith About Securities Fraud Investigation

BENSALEM, Pa.--(BUSINESS WIRE)--Law Offices of Howard G. Smith announces an investigation on behalf of Replimune Group Inc. (“Replimune” or the “Company”) (NASDAQ: REPL) investors concerning the Company's possible violations of federal securities laws.IF YOU ARE AN INVESTOR WHO SUFFERED A LOSS IN REPLIMUNE GROUP INC. (REPL), CONTACT THE LAW OFFICES OF HOWARD G. SMITH ABOUT POTENTIALLY PURSUING CLAIMS TO RECOVER YOUR LOSS.Contact the Law Offices of Howard G. Smith to discuss your legal rights by.

businesswire.com - 2026-07-29 15:04:00

Securities Fraud Investigation Into Replimune Group Inc. (REPL) Announced -- Shareholders Who Lost Money Urged To Contact The Law Offices of Frank R. Cruz

[url="]The Law Offices of Frank R. Cruz[/url] announces an investigation of Replimune Group Inc. (“Replimune” or the “Company”) (NASDAQ: [url="]REPL[/ur

gurufocus.com - 2026-07-28 21:00:00

Securities Fraud Investigation Into Replimune Group Inc. (REPL) Announced – Shareholders Who Lost Money Urged To Contact The Law Offices of Frank R. Cruz

LOS ANGELES--(BUSINESS WIRE)--The Law Offices of Frank R. Cruz announces an investigation of Replimune Group Inc. (“Replimune” or the “Company”) (NASDAQ: REPL) on behalf of investors concerning the Company's possible violations of federal securities laws.IF YOU ARE AN INVESTOR WHO LOST MONEY ON REPLIMUNE GROUP INC. (REPL), CLICK HERE TO INQUIRE ABOUT POTENTIALLY PURSUING A CLAIM TO RECOVER YOUR LOSS.What Is The Investigation About?On July 28, 2026, the US Food and Drug Administration (“FDA”) rel.

businesswire.com - 2026-07-28 20:40:00

Replimune Group, Inc. (REPL) Investors Who Suffered Losses Are Encouraged to Contact Johnson Fistel Following FDA Briefing Document

SAN DIEGO, July 28, 2026 (GLOBE NEWSWIRE) -- Johnson Fistel, PLLP is investigating whether Replimune Group, Inc. (NASDAQ: REPL) or certain of its executive officers violated state or federal securities laws. The investigation focuses on investors' losses and whether they may be recovered under federal securities laws.

globenewswire.com - 2026-07-28 18:21:00

Replimune Lead Drug Trial Data Deemed 'Not Interpretable' by FDA Staff

Replimmune Group Inc. (NASDAQ:REPL) stock is trading lower on Tuesday after the U.S. Food and Drug Administration released briefing documents related to the company's vusolimogene oderparepvec, or RP1, for skin cancer.

benzinga.com - 2026-07-28 14:09:33

Replimune shares fall after FDA reviewers raise doubts over RP1 melanoma drug efficacy

Replimune (NASDAQ: REPL) shares fell nearly 31% on Tuesday after US Food and Drug Administration (FDA) staff reviewers raised concerns over the effectiveness of the company's lead cancer therapy, RP1, ahead of a key advisory committee meeting. The decline followed the release of FDA briefing documents that questioned whether Replimune had provided sufficient evidence to demonstrate RP1's efficacy in advanced melanoma.

proactiveinvestors.com - 2026-07-28 13:04:19

Replimune shares fall after FDA reviewers raise doubts over RP1 melanoma drug efficacy

Replimune (NASDAQ: REPL) shares fell nearly 31% on Tuesday after US Food and Drug Administration (FDA) staff reviewers raised concerns over the...

proactiveinvestors.com - 2026-07-28 09:02:00

US FDA staff raise efficacy concerns on Replimune's skin cancer drug ahead of meeting

The U.S. FDA staff reviewers ‌raised concerns on the efficacy of Replimune's drug for a type ​of a skin cancer, ​ahead of their meeting on ⁠July 30, briefing documents ​showed on Tuesday.

reuters.com - 2026-07-28 07:47:25

Johnson Fistel, PLLP Investigates Claims on Behalf of Long-Term Shareholders of Replimune Group, Inc. (REPL)

SAN DIEGO, July 15, 2026 (GLOBE NEWSWIRE) -- Johnson Fistel, PLLP is investigating potential claims on behalf of current, long-term shareholders of Replimune Group, Inc. (NASDAQ: REPL) against certain of its officers and directors for alleged breaches of fiduciary duty.

globenewswire.com - 2026-07-15 11:28:00

Replimune: Stock Buoyant On Third Try At RP1 Approval - FDA AdCom May Be Crucial

Replimune Group, Inc. faces a pivotal FDA AdCom for RP1 after two prior rejections, with a final FDA approval decision expected August 2, 2026. RP1 demonstrated a 34% ORR and median overall survival of 32.9 months in anti-PD-1-failed melanoma, but trial design concerns persist. REPL stock has surged over 135% since April as FDA leadership changes and collaborative dialogue opened a path for BLA resubmission.

seekingalpha.com - 2026-06-30 10:09:50

Replimune Reports Fiscal Fourth Quarter and Year End 2026 Financial Results and Provides Corporate Update

WOBURN, Mass., June 29, 2026 (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, 2026 and provided a business update.

globenewswire.com - 2026-06-29 08:00:00

Replimune Announces FDA Acceptance of RP1 Biologics License Application Resubmission for Advanced Melanoma

WOBURN, Mass., June 26, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, announced today that the U.S. Food and Drug Administration (FDA) has accepted for review the resubmission of the Biologics License Application (BLA) for RP1 (vusolimogene oderparepvec) in combination with nivolumab for the treatment of advanced melanoma.

globenewswire.com - 2026-06-26 08:00:00

REPL Stock Soars on Plans of BLA Resubmission for Melanoma Combo Drug

Replimune stock surges after the company aligned with the FDA on plans to resubmit its BLA for RP1 plus Opdivo in advanced melanoma.

zacks.com - 2026-06-01 14:06:13

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

WOBURN, Mass., May 31, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today presented final first-in-human data for RP2 alone and in combination with nivolumab in patients with advanced solid tumors during an oral session at the 2026 American Society of Clinical Oncology annual meeting.

globenewswire.com - 2026-05-31 08:00:00

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

WOBURN, Mass., May 30, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today presented 3-year landmark overall survival data from the IGNYTE clinical trial of RP1 plus nivolumab in patients with anti-PD-1 failed melanoma during an oral session at the 2026 American Society of Clinical Oncology annual meeting.

globenewswire.com - 2026-05-30 08:00:00

How Replimune's drug got a third chance after the White House intervened

Replimune representatives met with White House officials in early May and by the end of month, the Food and Drug Administration was planning to review the melanoma medication again.

wsj.com - 2026-05-29 21:53:00

Replimune to resubmit twice-rejected drug for approval after FDA shakeup

Replimune said it plans to resubmit its melanoma drug for approval following two earlier rejections. The move follows the departure of Food and Drug Administration Commissioner Marty Makary.

cnbc.com - 2026-05-29 08:51:06

Replimune reaches agreement with US FDA to resubmit melanoma drug application

Replimune 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.

reuters.com - 2026-05-29 08:07:19

Replimune Announces Planned RP1 BLA Resubmission Following Productive Discussion with FDA

WOBURN, Mass., May 29, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced that following collaborative communications with the U.S. Food and Drug Administration (FDA), the Company and the FDA have aligned on a path forward for resubmission and reconsideration of the Biologics License Application (BLA) for RP1 (vusolimogene oderparepvec) in combination with nivolumab for the treatment of advanced melanoma.

globenewswire.com - 2026-05-29 08:00:00

Replimune Gets Third Try at FDA Approval After Makary Departure

Experimental melanoma drug was rejected twice because the Food and Drug Administration questioned its study design.

wsj.com - 2026-05-29 07:30:00

INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Replimune Group, Inc. - REPL

NEW YORK, May 21, 2026 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Replimune Group, Inc. ("Replimune" or the "Company") (NASDAQ: REPL).  Such investors are advised to contact Danielle Peyton at [email protected] or 646-581-9980, ext.

prnewswire.com - 2026-05-21 16:40:00

INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Replimune Group, Inc. - REPL

NEW YORK, May 19, 2026 (GLOBE NEWSWIRE) -- Pomerantz LLP is investigating claims on behalf of investors of Replimune Group, Inc. (“Replimune” or the “Company”) (NASDAQ: REPL).  Such investors are advised to contact Danielle Peyton at [email protected] or 646-581-9980, ext.

globenewswire.com - 2026-05-19 18:07:00

REPL Investors Have Opportunity to Join Replimune Group, Inc. Fraud Investigation with the Schall Law Firm

LOS ANGELES, May 17, 2026 (GLOBE NEWSWIRE) -- The Schall Law Firm, a national shareholder rights litigation firm, announces that it is investigating claims on behalf of investors of Replimune Group, Inc. ("Replimune" or "the Company") (NASDAQ: REPL) for violations of the securities laws.

globenewswire.com - 2026-05-17 21:49:05

REPL Investors Have Opportunity to Join Replimune Group, Inc. Fraud Investigation with the Schall Law Firm

LOS ANGELES, May 17, 2026 (GLOBE NEWSWIRE) -- The Schall Law Firm, a national shareholder rights litigation firm, announces that it is investigating claims on behalf of investors of Replimune Group, Inc. (“Replimune” or “the Company”) (NASDAQ: REPL) for violations of the securities laws. The investigation focuses on whether the Company issued false and/or misleading statements and/or failed to disclose information pertinent to investors.

globenewswire.com - 2026-05-17 21:49:00

INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Replimune Group, Inc. - REPL

NEW YORK, May 14, 2026 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Replimune Group, Inc. ("Replimune" or the "Company") (NASDAQ: REPL). Such investors are advised to contact Danielle Peyton at [email protected] or 646-581-9980, ext.

prnewswire.com - 2026-05-14 20:15:00

Replimune: Perhaps The FDA Shakeup Will Get A Mulligan For RP1

Replimune Group, Inc.'s RP1 has failed at the FDA twice, but Makary's resignation keeps a resubmission possible. REPL's cash runway stands at under a year; workforce cuts and RP1 discontinuation are being considered. I maintain a cautious Buy on the ability for REPL to court surprising, bold turnarounds. I don't think this story is over.

seekingalpha.com - 2026-05-13 13:00:49

INVESTOR ALERT: Pomerantz Law Firm Investigates Claims on Behalf of Investors of Replimune Group, Inc. – REPL

NEW YORK, May 12, 2026 (GLOBE NEWSWIRE) -- Pomerantz LLP is investigating claims on behalf of investors of Replimune Group, Inc. (“Replimune” or the “Company”) (NASDAQ: REPL). Such investors are advised to contact Danielle Peyton at [email protected] or 646-581-9980, ext. 7980.

globenewswire.com - 2026-05-12 17:24:00

INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Replimune Group, Inc. - REPL

NEW YORK, May 7, 2026 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Replimune Group, Inc. ("Replimune" or the "Company") (NASDAQ: REPL). Such investors are advised to contact Danielle Peyton at [email protected] or 646-581-9980, ext.

prnewswire.com - 2026-05-07 10:00:00

What's Going On With Replimune Stock On Tuesday?

U.S. Food and Drug Administration (FDA) Commissioner Marty Makary defended his leadership in a CNBC interview aired Tuesday, growing criticism with concerns centering on drug approval decisions and internal leadership disputes that have sparked political and public backlash.

benzinga.com - 2026-05-05 13:44:49

FDA Commissioner Makary defends agency's decision on Replimune's drug

U.S. Food and Drug ​Administration Commissioner Dr. ‌Marty Makary on Tuesday defended ​the agency's ​decision to not approve ⁠Replimune's drug ​for advanced ​skin cancer.

reuters.com - 2026-05-05 10:58:49

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REPL Price Target Summary

Last Month

$12.00

1 analysts

Last Quarter

$12.33

3 analysts

Last Year

$13.14

7 analysts

All Time

$24.67

18 analysts

REPL Recent Analyst Grades

Date Analyst Firm Action Previous Grade New Grade
2026-06-30 Wedbush Maintain Neutral Neutral
2026-06-01 Wedbush Maintain Neutral Neutral
2026-04-13 Cantor Fitzgerald Downgrade Overweight Neutral
2026-04-13 Wedbush Downgrade Outperform Neutral
2026-04-13 JP Morgan Downgrade Neutral Underweight
2026-04-13 HC Wainwright & Co. Downgrade Buy Sell
2026-04-13 Jefferies Downgrade Buy Hold
2026-04-13 Leerink Partners Downgrade Outperform Market Perform
2026-02-05 Piper Sandler Maintain Overweight Overweight
2026-02-04 Wedbush Maintain Outperform Outperform