Replimune Announces Pricing of $150 Million Underwritten Offering
Replimune (Nasdaq: REPL) priced an underwritten offering of 9,701,490 common shares at $12.06 per share and pre-funded warrants to purchase 2,736,340 shares at $12.0599 per warrant.
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Rhea-AI Summary
Replimune (Nasdaq: REPL) priced an underwritten offering of 9,701,490 common shares at $12.06 per share and pre-funded warrants to purchase 2,736,340 shares at $12.0599 per warrant. Expected aggregate gross proceeds are about $150 million, before underwriting discounts, commissions, and expenses.
All securities will be sold by Replimune, with closing expected on August 11, 2026, subject to customary conditions. Leerink Partners, J.P. Morgan, and Cantor are acting as joint bookrunning managers under an effective shelf registration on Form S-3.
Positive
- $150 million expected gross proceeds before fees and expenses
- Underwritten sale of 9,701,490 shares at $12.06 each
- Pre-funded warrants for 2,736,340 shares priced at $12.0599
- Offering led by three bookrunning managers: Leerink Partners, J.P. Morgan, Cantor
Negative
- Issuance of 9,701,490 new shares plus 2,736,340 warrant shares will dilute existing shareholders
- Net proceeds will be below the stated $150 million gross due to underwriting discounts and offering expenses
News Explained
The priced offering could reduce existing ownership percentages and equals 240.4 days of the latest quarter’s operating cash use before transaction costs.
The offering is priced but has not closed; Replimune is the seller, and issuing the shares and any shares from exercised warrants would reduce existing holders’ percentage ownership.
A pre-funded warrant is sold at nearly the common-share price with a nominal exercise price and converts into shares when exercised, making these warrants an additional share-issuance mechanism.
For scale, the
Sources and calculations
- Replimune Announces Pricing of $150 Million Underwritten Offering (2026-08-10)
- Dilution (2026-07-17)
- Pre-funded warrant (2026-07-17)
- Replimune latest-quarter fundamentals (2026Q4)
- Offering gross against the last reported quarterly operating outflow, in days at that rate $150,000,000 / ($56,161,000 / 90) = 240.4 days
Details
Market move: REPL +13.35% in the Aug 10 session. underwritten public offering
On Aug 10, the day this news came out, REPL closed 13.35% above the previous close. Argus tracked a peak move of +22.4% during that session. Argus tracked a trough of -4.7% from its starting point during tracking. Our momentum scanner recorded 38 alerts for this stock that day.
Data tracked by StockTitan Argus for the Aug 10 session.
Key Figures
- Common shares offered
- 9,701,490 shares
- Underwritten offering
- Common share offering price
- $12.06 per share
- Underwritten offering
- Pre-funded warrant shares
- 2,736,340 shares
- In lieu of common stock for certain investors
- Pre-funded warrant purchase price
- $12.0599 per warrant
- Underwritten offering
- Warrant exercise price
- $0.0001 per share
- Pre-funded warrants
- Gross proceeds
- Approximately $150 million
- Before underwriting discounts, commissions, and expenses
- Expected closing date
- August 11, 2026
- Subject to customary closing conditions
Previous Offering Reports
-
Upsized public offering of common shares and pre-funded warrants
-
Proposed public offering of common stock and pre-funded warrants
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Key Terms
underwritten offering financial
pre-funded warrants financial
shelf registration statement regulatory
form s-3 regulatory
AI-generated analysis. How Rhea-AI works. Not financial advice.
BOSTON, Aug. 10, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (Nasdaq: REPL) (“Replimune”), a commercial-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced the pricing of an underwritten offering of 9,701,490 shares of its common stock at an offering price of
Leerink Partners, J.P. Morgan, and Cantor are acting as the bookrunning managers for the offering.
The securities are being offered by Replimune pursuant to its shelf registration statement on Form S-3, including a base prospectus, that was previously filed by Replimune with the Securities and Exchange Commission (the “SEC”) on May 23, 2025, as amended by Amendment No. 1 to the Registration Statement on Form S-3 filed with the SEC on November 6, 2025. A prospectus supplement relating to the offering, and the accompanying prospectus, will be filed with the SEC. Copies of the final prospectus supplement and the accompanying prospectus relating to the offering may be obtained, when available, by visiting EDGAR on the SEC website at www.sec.gov. Alternatively, copies of the prospectus supplement and the accompanying prospectus, when available, may be obtained from Leerink Partners LLC, Attention: Syndicate Department, 53 State Street, 40th Floor, Boston, Massachusetts 02109, by telephone at (800) 808-7525, ext. 6105, or by email at syndicate@leerink.com; J.P. Morgan Securities LLC, Attention: c/o Broadridge Financial Solutions, 1155 Long Island Avenue, Edgewood, NY 11717, or email: prospectus-eq_fi@jpmchase.com and postsalemanualrequests@broadridge.com; and Cantor Fitzgerald & Co., Attention: Equity Capital Markets, 110 East 59th Street, 6th Floor, New York, New York 10022, or by email at prospectus@cantor.com.
This press release shall not constitute an offer to sell or the solicitation of an offer to buy, nor shall there be any sale of securities, in any state or jurisdiction in which such an offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.
About Replimune
Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of novel oncolytic immunotherapies, including the Company’s first commercially available product TUDRIQEVTM (vusolimogene oderparepvec-wtpg), approved under accelerated approval by the U.S. Food and Drug Administration in combination with nivolumab for the treatment of adults with advanced melanoma who experienced disease progression on a PD-1 antibody-based regimen. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and induce a systemic anti-tumor immune response. Upon intratumor injection, RPx causes direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens, alteration of the tumor microenvironment, and when dosed in combination with an immune checkpoint inhibitor immunotherapy, it may ignite a systemic anti-tumor response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options.
Forward-Looking Statements
This press release contains forward looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, including statements regarding the timing of closing of our offering, the gross proceeds we expect to receive from our offering and other statements identified by words such as “could,” “expects,” “intends,” “may,” “plans,” “potential,” “should,” “will,” “would,” or similar expressions and the negatives of those terms. Forward-looking statements are not promises or guarantees of future performance and are subject to a variety of risks and uncertainties, many of which are beyond our control, and which could cause actual results to differ materially from those contemplated in such forward-looking statements. These factors include risks related to our limited experience in commercializing products for sale, our ability to successfully verify the clinical benefit of TUDRIQEV in our ongoing confirmatory Phase 3 trial, IGNYTE-3, our ability to meet our product manufacturing goal, the timing and scope of future regulatory approvals, the availability of combination therapies needed to conduct our clinical trials, changes in laws and regulations to which we are subject, competitive pressures, our ability to identify additional product candidates, the impact of political and global macro factors and military conflicts, and other risks as may be detailed from time to time in our Annual Reports on Form 10-K and Quarterly Reports on Form 10-Q and other reports we file with the Securities and Exchange Commission. Our actual results could differ materially from the results described in or implied by such forward-looking statements. Forward-looking statements speak only as of the date hereof, and, except as required by law, we undertake no obligation to update or revise these forward-looking statements.
Investor Inquiries
Chris Brinzey
ICR Westwicke
339.970.2843
chris.brinzey@westwicke.com
Media Inquiries
Arleen Goldenberg
Replimune
917.548.1582
media@replimune.com
FAQ
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