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1
institution
Market cap
$960.3M
83M shares
52-week range
$1.50 – $13.24
83% from low
Sector
BIOLOGICAL PRODUCTS, (NO DIAGNOSTIC SUBSTANCES)
Exchange
NASDAQ
CS
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| 2019 | 2020 | 2021 | 2022 | 2023 | 2024 | 2025 | 2026 | |
|---|---|---|---|---|---|---|---|---|
| Revenue | $0 | $0 | $0 | $0 | $0 | $0 | $0 | $0 |
| Cost of revenue | $148.0K | $0 | $4.1M | $4.6M | $0 | $0 | $0 | $0 |
| Gross profit | −$148.0K | $0 | −$4.1M | −$4.6M | $0 | $0 | $0 | $0 |
| Gross margin | — | — | — | — | — | — | — | — |
| R&D | $22.2M | $38.8M | $57.5M | $80.6M | $126.5M | $175.0M | $189.4M | $221.2M |
| Operating income | −$30.9M | −$56.2M | −$82.8M | −$121.5M | −$177.1M | −$234.8M | −$261.6M | −$319.9M |
| EBITDA | −$30.7M | −$52.6M | −$76.5M | −$114.4M | −$171.7M | −$227.8M | −$253.9M | −$314.5M |
| Net income | −$30.8M | −$52.6M | −$80.9M | −$118.0M | −$174.3M | −$215.8M | −$247.3M | −$313.9M |
| Net margin | — | — | — | — | — | — | — | — |
| EPS (diluted) | -1.33 | -1.54 | -1.75 | -2.26 | -2.99 | -3.24 | -3.07 | -3.38 |
Annual figures · source: Financial Modeling Prep
| Year | Est. revenue | Est. EPS | EPS range | # Analysts |
|---|---|---|---|---|
| 2027 | $12M | $-1.84 | $-2.22–$-1.07 | 5 |
| 2028 | $40M | $-1.16 | $-2.01–$-0.37 | 5 |
| 2029 | $158M | $-0.69 | $-1.20–$-0.01 | 4 |
| 2030 | $193M | $-0.42 | $-1.26–$0.05 | 2 |
Forward consensus · source: Financial Modeling Prep
Replimune Group Inc is a clinical-stage biotechnology company. It uses a proprietary RPx platform to design and develop product candidates that are intended to maximally activate the immune system against solid tumors. The RPx platform is based on a proprietary, engineered strain of herpes simplex virus 1, or HSV-1, backbone with payloads added to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The company focuses on developing oncolytic immunotherapies for the treatment of cancer. Its pipeline products include RP1, RP2, and RP3. The company operates in USA and UK, majority of revenue from USA.
www.replimune.comNo one on the platform currently holds REPL.
| Institution | Shares | Reported |
|---|---|---|
| Renaissance Technologiesas of 2026-03-31 | 381,453 | $2.9M |
| Execution date | Ratio |
|---|---|
| 2010-12-01 | 15-for-1 |
No one on the platform has traded REPL yet.
| $667M |
| — |
| IOVAIovance Biotherapeutics, Inc. | $4.21 | -0.94% | $1.5B | — |
| MBXMBX Biosciences, Inc. Common Stock | $53.85 | +2.94% | $1.8B | — |
Source: Financial Modeling Prep · peers by sector/industry
Click to see transaction details on SEC.gov. Form 4s cover trades by officers, directors, and 10%+ owners, due within 2 business days of the trade.
$CAPR Three Nasdaq Biotech Stories That Matter Now: $UNCY’s OLC PDUFA, $CAPR’s FDA AdCom, and $REPL’s RP1 Resubmission https://www.merlintrader.com/biotech-radar-jun29/
View on StockTwits ↗$REPL “DOWN GOES FRAZIER….DOWN GOES FRAZIER”!!!!
View on StockTwits ↗$REPL - Replimune Group Inc - 10K - Updated Risk Factors REPL’s risk profile has intensified: RP1’s BLA for advanced melanoma has now twice been hit with FDA CRLs and faces an advisory committee before an August 2, 2026 action date, with no assurance of approval; leadership churn and policy shifts at FDA, possible foreign knock-on effects, potential RP1 restructuring fallout, and expanded global privacy/AI compliance risks further cloud the path to commercialization and funding. #Biotech #FDARegulatoryRisk #Oncology #DrugApprovalDelay #DataPrivacy 🟢 Added 🟠 Removed https://d-risk.ai/REPL/10-K/2026-06-29
View on StockTwits ↗$REPL looks like they cut 55% of workforce after 2nd CRL
View on StockTwits ↗$REPL this one is new after the lawsuit: Without an accelerated approval of the BLA for RP1 in combination with nivolumab for the treatment of advanced melanoma from this resubmitted BLA we might not be able to continue the development of RP1 for this indication, if at all, and we may be required to implement a restructuring plan and review our priorities across the RPx portfolio and the company as a whole.
View on StockTwits ↗@Daddy044 @bnglao24 Fair questions, The 3 designations + a real unmet do lower the odds of an FDA roadblock. Though, RMAT/BTD guarantee frequent FDA contact and open the accelerated lane, they stop short of pre-validating that single-arm + hem CR/MRD is enough. This gets settled at the pre-BLA meeting and PDUFA, and stays non-binding till then. $REPL Aug 2 PDUFA should be a live read on FDA's single-arm appetite, and note that IMMX is a cleaner case: monotherapy, so no contribution-of-effect issue like RP1's combo. Landau, still said approval "can't be guaranteed" and that regulators lean randomized. From this I do read : Residual risk = still nonzero
View on StockTwits ↗$REPL - regardless of what you think about RP1's utility, pretty cool to see swift acceptance of BLA resubmission with Adcom in late July and August 2nd PDUFA An efficient, agile FDA is clearly a positive for the sector $XBI
View on StockTwits ↗$REPL released its Q4 and full-year 2026 financial results in a news release attached to the 8-K.
View on StockTwits ↗$REPL Either BEACHSIDEFREDDY or JP MORGAN are going to play the fool. May be factual may be cruel but everybody plays the fool. JP MORGAN FOOL
View on StockTwits ↗$REPL 10-K filing https://www.sec.gov/ix?doc=/Archives/edgar/data/1737953/000162828026045886/repl-20260331.htm
View on StockTwits ↗$REPL Replimune Reports Fiscal Fourth Quarter and Year End 2026 Financial Results and Provides Corporate Update https://www.globenewswire.com/news-release/2026/06/29/3318910/0/en/replimune-reports-fiscal-fourth-quarter-and-year-end-2026-financial-results-and-provides-corporate-update.html "Based on the current operating plan, the Company believes that existing cash, cash equivalents and short-term investments will enable us to fund operations into the first quarter of calendar 2027, which includes scale up for the potential commercialization of RP1 in skin cancers and for working capital and general corporate purposes and excludes any potential revenue."
View on StockTwits ↗$IMMX NXC-201 thesis keeps tightening : - Landau's latest: standing 95% CR (19/20 mature), pathologic light chains normalizing by a med of 7 days, low-grade CRS reversed with toci, zero neurotoxicity including delayed. Trial now complete at 42 pts, no dose-limiting tox. She flags the usual worry that regulators lean toward randomized trials, but RMAT + BTD formally open the accelerated path, the 95% magnitude carries the persuasiveness, and 1-yr durability backs the surrogate IMO. - CMC is the quiet topic nobody discussed. However: 14-day vein-to-vein in 100% of pts (industry runs 30+), and a full-time CMC lead, Davis-Pickett, ex-Juno/Breyanzi, who carried Module 3 through to BLA. - Plenty of cash, dilution digested. Sept 2026 update, then 1-yr data circa Mar 2027 drives the BLA. Watching the pre-BLA meeting (Q4 '26?). Also watching $REPL Aug 2 PDUFA — first real test of FDA's appetite for single-arm data post its June draft guidance. IMMX data is cleaner than REPL btw.
View on StockTwits ↗Recent $TICKER stream from stocktwits.com — refreshed every 5 minutes. Sentiment tags are self-reported by posters. Not investment advice.