REPL logo

REPLIMUNE GROUP INC

REPLNASDAQ
๐Ÿ† #2042 by market capEarnings Nov 4US Equity
$13.65โ–ผ $0.02 (โˆ’0.15%)
๐ŸŒ… Pre-market$13.59โ–ผ 0.44%Regular close ยท extended-hours price shown
1hโ€”
24hโ–ผ 0.1%
7dโ–ฒ 15.3%
14dโ–ฒ 151.6%
30dโ–ฒ 37.3%
1yโ–ฒ 160.0%
๐ŸฆMarket Cap
$1.15B
Small Cap
๐Ÿ“ˆRevenue Growth (YoY)
โ€”
๐Ÿ“ŠGross Margin
โ€”
๐Ÿ’ตFCF Margin
โ€”
โš–๏ธP/S Ratio
โ€”
Otter Score
58
Weak

Trading Snapshot

Day Range
$13.50 โ€“ $13.80
52-Week Range
$1.50 โ€“ $14.12
Volume
$5.10B
Avg Volume
$6.27B
Shares Outstanding
84.0M
Next Earnings
Oct 11, 2026

Fundamentals Snapshot

Annual Revenue
$201M
Last Q Revenue
$48M
P/E Ratio
โ€”
P/S Ratio
โ€”
EPS (TTM)
$-3.39
Dividend Yield
โ€”

Why Investors Own REPL

  • โœ“High-growth profile โ€” revenue up -1.8% YoY with expanding US Equity exposure.
  • โœ“Healthy economics โ€” 58% gross margin and 29% free-cash-flow margin.
  • โœ“New products and segments could unlock additional revenue streams.
โš ๏ธ Key Risks

Execution delays, intensifying competition, and valuation compression if growth decelerates.

Financial Trends

Revenue (TTM)
$201Mโ–ผ โˆ’0.8% YoY
Gross Margin (TTM)
58.1%โ–ฒ +2.5% YoY
Operating Income (TTM)
$44Mโ–ผ โˆ’0.8% YoY
Free Cash Flow (TTM)
$59Mโ–ผ โˆ’0.8% YoY

About REPLIMUNE GROUP INC

Replimune Group, Inc. is a biotechnology enterprise dedicated to pioneering oncolytic immuno-gene therapies aimed at treating various cancers. The company leverages its proprietary Immunotherapy platform to engineer and advance novel therapeutic candidates designed to activate the body's immune system against malignant cells. Its leading experimental drug, RP1, is a selectively replicating variant of the herpes simplex virus 1. This candidate is presently in Phase I/II clinical trials for a range of solid tumors and has also progressed to Phase II trials specifically for patients with cutaneous squamous cell carcinoma. Replimune is additionally developing RP2, an anti-CTLA-4 antibody-like protein, which is undergoing Phase I clinical assessment. Its purpose is to counteract the immune system's suppression often mediated by CTLA-4. Furthermore, RP3, also in Phase I clinical trials, is engineered to express immune-activating proteins that stimulate T cells. Established in 2015, Replimune Group, Inc. maintains its corporate headquarters in Woburn, Massachusetts.

๐Ÿฆฆ

Otter Score Breakdown

โ“˜
๐Ÿ’ŽQualityโ˜…โ˜…โ˜…โ˜…โ˜…
๐Ÿš€Growthโ˜…โ˜…โ˜…โ˜…โ˜…
โš–๏ธValuationโ˜…โ˜…โ˜…โ˜…โ˜…
โšกMomentumโ˜…โ˜…โ˜…โ˜…โ˜…
Overall Score
Weak
58/100

Analyst Ratings

โ“˜
Consensus
Buy
14 analysts
Strong Buy4
Buy7
Hold2
Sell1
Strong Sell0
Ratings as of Aug 2026

Latest News & Updates

๐Ÿš€
Benzingaยท2d ago

Replimune Prices ~$150M Underwritten Offering Of 9,701,490 Shares And Warrants At $12.06 Per Unit

The aggregate gross proceeds from the offering are expected to be approximately $150 million, before deducting underwriting discounts and commissions and other offering expenses. All of the securities in the offering

๐Ÿ›ฐ๏ธ
Benzingaยท4d ago

Wedbush Upgrades Replimune Group to Outperform, Raises Price Target to $19

Wedbush analyst Robert Driscoll upgrades Replimune Group (NASDAQ:REPL) from Neutral to Outperform and raises the price target from $12 to $19.

SeekingAlphaยท4d ago

Replimune Group, Inc. (REPL) Shareholder/Analyst Call Transcript

Replimune Group, Inc. (REPL) Shareholder/Analyst Call August 6, 2026 4:30 PM EDTCompany ParticipantsArleen GoldenbergSushil Patel - CEO &...

Benzingaยท5d ago

Two Rejections, Messy Process: Replimune Finally Secures FDA Approval for Skin Cancer Treatment

FDA grants Replimune accelerated approval for TUDRIQEV in combination with nivolumab to treat advanced cutaneous melanoma.

SeekingAlphaยท5d ago

Replimune Group, Inc. (REPL) Shareholder/Analyst Call - Slideshow

2026-08-07. The following slide deck was published by Replimune Group, Inc.

๐ŸŒŒ
Benzingaยท5d ago

Replimune Receives FDA Accelerated Approval For TUDRIQEVTM In Combination With Nivolumab For Treatment Of Adults With Unresectable Advanced Cutaneous Melanoma

Replimune Group, Inc. (NASDAQ:REPL), a commercial stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced that the U.S. Food and Drug Administration (FDA) has granted