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Replimune/$REPL

1D1W1M3M6MYTD1Y5YMAX

About Replimune

Replimune Group Inc is a clinical-stage biotechnology company committed to applying its expertise in the field of oncolytic immunotherapy to transform the lives of cancer patients through novel oncolytic immunotherapies. Its proprietary oncolytic immunotherapy product candidates are designed and intended to maximally activate the immune system against cancer. Oncolytic immunotherapy is an emerging drug class. The proprietary RPx platform is based on a novel, engineered strain of herpes simplex virus 1, or HSV-1, backbone with payloads added that are intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. It operates in single segment of developing oncolytic immunotherapies for the treatment of cancer.
Ticker
$REPL
Sector
Health
Primary listing
NASDAQ
Employees
465

Replimune Metrics

BasicAdvanced
$1B
-
-$3.15
0.94
-

What the Analysts think about Replimune

Analyst ratings (Buy, Hold, Sell) for Replimune stock.
Analyst projections of the future price of Replimune stock.

Bulls say / Bears say

FDA accelerated approval gives Replimune its first marketed medicine for advanced melanoma after prior regulatory setbacks. The company expects to launch TUDRIQEV in the US within 60 days, creating a route to product revenue. (Reuters, Replimune)
The RP1 combination has shown potentially durable activity in a hard-to-treat group: 47.8% of all treated patients were alive at three years, with median overall survival of 32.9 months. An FDA advisory committee also voted 10-3 that the efficacy results were evaluable and clinically meaningful. (Replimune, Replimune)
RP2 gives Replimune a second potential growth engine beyond TUDRIQEV. In first-in-human data, RP2 plus nivolumab produced a 19.1% response rate and 48.9% disease-control rate, supporting the ongoing randomised Phase 2/3 REVEAL trial in metastatic uveal melanoma. (Replimune, Replimune)
The FDA previously said RP1's single-arm trial made it unclear whether the drug itself drove the tumour responses, and warned that the reported response rate might be artificially inflated. That leaves the strength of the approval evidence disputed despite the eventual authorisation. (Reuters)
TUDRIQEV's accelerated approval depends on a confirmatory trial proving clinical benefit, so it is not fully de-risked. Replimune says the Phase 3 trial's primary overall-survival readout is expected in 2030, leaving a long period in which a failed study could threaten the approval. (Replimune, Last10K)
The business remains cash-burning as it moves into commercialisation: Replimune reported a $69.8 million quarterly net loss and said more than 12 months of funding included $141 million of net proceeds from a common-stock issue. Further development and launch costs could therefore bring more financing needs and shareholder dilution. (Last10K)
Data summarised monthly by Lightyear AI. Last updated on 23 Sept 2026.

Replimune Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Replimune Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise

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