Replimune Group, Inc.
NASDAQ•REPL
CEO: Mr. Philip Astley-Sparke F.S.A.
Sector: Healthcare
Industry: Biotechnology
Listing Date: 2018-07-20
Replimune Group, Inc., a clinical-stage biotechnology company, focuses on the development of oncolytic immunotherapies to treat cancer. The company's proprietary tumor-directed oncolytic immunotherapy product candidates are designed and intended to activate the immune system against cancer. Its lead product candidate is RP1, a selectively replicating version of HSV-1 that expresses GALV-GP R(-) and human GM-CSF, which is in Phase I/II clinical trials for a range of solid tumors. The company is also developing RP2, which is in Phase I clinical trials to express an anti-CTLA-4 antibody-like protein to block the inhibition of the immune response otherwise caused by CTLA-4; and RP3 that is in Phase I clinical trial to express immune-activating proteins that stimulate T cells. Replimune Group, Inc. was founded in 2015 and is headquartered in Woburn, Massachusetts.
Contact Information
Market Cap
$308.82M
P/E (TTM)
-1.1
22.3
Dividend Yield
--
52W High
$13.24
52W Low
$1.50
52W Range
Rank58Top 85.6%
2.3
F-Score
Modified Piotroski Analysis
Based on 9-year fundamentals
Weak • 2.3 / 9 points
Scoring Range (0-9)
8-9: Excellent Value
6-7: Strong Fundamentals
4-5: Average Quality
0-3: Weak Performance
Data Period: 2017-2025
Financial Dashboard
Q3 2026 Data
Revenue
$0.00+0.00%
4-Quarter Trend
EPS
-$0.77+0.00%
4-Quarter Trend
FCF
-$66.09M+0.00%
4-Quarter Trend
2026 Q3 Earnings Highlights
Key Highlights
R&D Spending Ramps Up Nine-month R&D expenses reached $168.9M, increasing $33.4M, driven by RP1 confirmatory study costs and RP2 enrollment.
Operating Loss Widens Nine-month net loss totaled $(240.7M)$, significantly wider than prior year's $(173.2M)$ loss due to increased operating costs.
SG&A Prepares Launch SG&A expenses grew $30.9M to $77.7M for nine months, reflecting pre-commercial infrastructure buildout and personnel costs.
Cash Runway Extended Cash runway extends past 12 months, supported by $35.0M debt draw and $20.8M January ATM proceeds.
Risk Factors
Regulatory Approval Uncertainty RP1 BLA resubmission review ongoing with PDUFA date set for April 10, 2026; negative outcome risks viability.
Internal Control Material Weakness Identified material weaknesses in IT general controls; remediation efforts are ongoing but not yet fully effective.
High Cash Burn Rate Net cash used in operating activities increased to $(224.2M)$ for nine months, requiring continued external financing.
Commercialization Hurdles Remain Success depends on market acceptance, reimbursement, and competition, especially if RP1 faces further regulatory limitations.
Outlook
RP1 BLA Review Status Evaluating FDA feedback following BLA resubmission; next steps determined by April 2026 PDUFA decision timeline.
Advancing RP2/RP3 Pipeline Enrolling patients in RP2 REVEAL study expansion and planning preliminary data release for RP2 HCC cohort by end of 2026.
Funding Operations Forecast Current capital, including recent debt/equity raises, expected to fund operations through at least Q1 2027.
Continued High Operating Costs Expect continued substantial expenses and increasing operating losses for at least the next several years due to development.
Peer Comparison
Revenue (TTM)
$285.61M
$197.09M
$141.31M
Gross Margin (Latest Quarter)
9793.1%
100.0%
100.0%
Key Metrics
Symbol | Market Cap | P/E (TTM) | ROE (TTM) | Debt to Assets |
|---|---|---|---|---|
| VIR | $1.57B | -3.1 | -53.3% | 8.4% |
| IOVA | $1.32B | -4.4 | -50.2% | 5.1% |
| MGTX | $916.32M | -7.0 | 4438.9% | 36.3% |
Long-Term Trends
Last 4 Quarters
Revenue
Net Income
Operating Cash Flow
4Q Revenue CAGR
N/M
Revenue Volatile
4Q Net Income CAGR
N/M
Profitability Shift
Cash Flow Stability
0%
Cash Flow Needs Attention
Deep Research
Next earnings:May 14, 2026
EPS:-$0.71
|Revenue:$948.01K
Financials
Earnings Calls
Reports
News
Income Statement
Balance Sheet
Cash Flow Statement
Ratios
% Chg.
Income Statement | LTM |
|---|
No Data