Replimune Group, Inc.

Replimune Group, Inc.

REPL
Replimune Group, Inc.US flagNASDAQ Global Select
11.00
USD
+0.49
- -
923.40MMarket Cap
2017 Y
2018 Y
2019 Y
2020 Y
2021 Y
2022 Y
2023 Y
2024 Y
2025 Y
2026 Y
TTM
Revenue per Share
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Basic EPS, GAAP
-0.36
-0.92
-1.33
-1.54
-1.75
-2.26
-2.99
-3.24
-3.07
-3.38
-3.42
Free Cash Flow per Basic Share
-0.34
-0.75
-1.21
-1.96
-1.38
-1.62
-2.24
-2.87
-2.47
-3.07
-3.1
Dividend per Share
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Book Value per Share
-0.43
-1.35
-2.57
-3.28
-4.18
-5.96
-8.34
-10.53
-11.77
-13.6
-13.74
Tangible Book Value per Share
-0.54
-1.31
5.94
5.36
10.78
7.88
9.54
5.63
5.16
1.79
1.81
Basic Weighted Avg Shares
22
22
23
34
46
52
58
67
81
93
92
Sales/Revenue/Turnover
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Operating Margin (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Depreciation Expense
- -
- -
- -
1
2
2
2
3
4
3
3
Net Income, GAAP
-8
-20
-31
-53
-81
-118
-174
-216
-247
-314
-314
Effective Tax Rate (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Profit Margin (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Working Capital
20
60
131
162
469
383
559
393
434
221
221
LT Debt
- -
- -
- -
39
30
29
57
72
72
108
108
Total Equity
-12
-28
138
184
499
411
555
375
416
166
166
Return on Invested Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Return on Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Return on Common Equity (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -

Capital Structure

FRC

in mil. unless spec.
Sep'26
Dec'26
Mar'26
ST Debt
4
4
4
LT Borrowings
47
48
83
LT Finance Leases
25
25
24
Preferred Equity and Hybrid Capital
- -
- -
- -
Shares Outstanding
78
80
83
Market Capitalization
373
893
703

Working Capital

FRC

in mil. unless spec.
Sep'26
Dec'26
Mar'26
Total Current Assets
334
280
279
Cash, Cash Equivalents & STI
324
269
269
Accounts Receivable, Net
- -
- -
- -
Inventories
- -
- -
- -
Total Current Liabilities
53
50
58
Payables & Accruals
31
30
34
ST Debt
4
4
4
Deferred Revenue
- -
- -
- -

Growth Rates

FRC

in mil. unless spec.

(avg. rate of change)

10 years
5 years
1 year
Total Equity
- -
-12.81%
-60.04%
Free Cash Flow
- -
36.1%
43.04%
Net Income, GAAP
- -
31.8%
26.95%
Sales/Revenue/Turnover
- -
- -
- -
Total Cash Common Dividend
- -
- -
- -

Quarterly Revenue

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -

Quarterly Earnings Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
-0.75
-0.9
-0.77
- -
-3.24
2025
-0.78
-0.68
-0.79
- -
-3.07
2026
-0.95
-0.9
-0.77
- -
-3.38

Quarterly Dividends Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -

Company Description

APIChatGPT
CEO
Sushil Patel
Full Time Employees
465
Sector
Healthcare
Industry
Biotechnology
Address
500 Unicorn Park Drive Woburn MA United States of America 01801
IPO Date
Jul 20, 2018
Business
Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company, develops oncolytic immunotherapies based on its proprietary RPx platform, which utilizes an engineered herpes simplex virus 1 (HSV-1) backbone to selectively replicate in and destroy tumor cells while stimulating systemic anti-tumor immune responses; its lead product candidate RP1 (vusolimogene oderparepvec) expresses GALV-GP R(-) and human GM-CSF for treating solid tumors including advanced melanoma; RP2 incorporates an anti-CTLA-4 antibody-like protein to enhance T-cell activation; and RP3 expresses multiple immune-activating transgenes including anti-CTLA-4 and immune stimulatory proteins to further potentiate immune responses against cancer. Founded in 2015 and headquartered in Woburn, Massachusetts, the company conducts operations primarily in the United States and the United Kingdom, targeting patients with solid tumors such as melanoma, skin, and other cancers through clinical-stage programs often in combination with checkpoint inhibitors like nivolumab (Opdivo). In recent developments, Replimune submitted a biologics license application (BLA) to the U.S. FDA for RP1 plus nivolumab in advanced melanoma post-anti-PD1 therapy, which received priority review before a complete response letter (CRL) in July 2025; the company resubmitted the BLA in October 2025 with additional data and analyses addressing FDA feedback, earning acceptance and a PDUFA target action date of April 10, 2026; additionally, it announced a proposed $125 million public offering of common stock in November 2024, with a 30-day underwriter option for $18.75 million more, to fund clinical development and operations.

Company News

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

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

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

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

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

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

  • 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

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

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

  • Replimune reaches agreement with US FDA to resubmit melanoma drug application

  • Replimune Announces Planned RP1 BLA Resubmission Following Productive Discussion with FDA

  • Replimune Gets Third Try at FDA Approval After Makary Departure

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

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

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

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

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

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