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Replimune Group reported a $313.9M net loss for fiscal 2026. See the full REPL financial statements: income statement, balance sheet, cash flow and ratios, each column linked to its SEC filing.

Replimune to Present at the Cantor Global Healthcare Conference 2026

Replimune will webcast its Cantor Global Healthcare Conference fireside chat for investors with a 30-day replay window.

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Replimune (REPL) will participate in a fireside chat at the Cantor Global Healthcare Conference on Thursday, September 10 at 9:10 AM ET.

The presentation will be webcast live in the Investors section of Replimune’s website, with a replay available online for 30 days following the conference.

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Positive

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Negative

  • None.

Market Context

The August 6 FDA-approval announcement was followed by -6.22%, while the July 30 advisory-committee ...
Analysis

The August 6 FDA-approval announcement was followed by -6.22%, while the July 30 advisory-committee update was followed by 107.02% in the platform record. This conference notice adds no new data; the active S-3ASR shelf remains relevant financing context.

Key Figures

Announcement date: September 3, 2026 Conference date: September 10 Presentation time: 9:10 AM ET +1 more
4 metrics
Announcement date September 3, 2026 Article dateline
Conference date September 10 Cantor Global Healthcare Conference
Presentation time 9:10 AM ET Fireside chat
Replay availability 30 days Following the conference

Historical Context

5 past events · Latest: Aug 19 (Neutral)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Aug 19 Inducement equity grants Neutral -5.1% Company granted inducement options and restricted stock units to its chief commercial officer.
Aug 14 Q1 2027 earnings Positive -1.4% Quarterly loss narrowed while cash and financing proceeds supported more than twelve months.
Aug 10 Underwritten offering Negative +13.3% Company priced common shares and pre-funded warrants for aggregate gross proceeds.
Aug 06 FDA accelerated approval Positive -6.2% FDA authorized TUDRIQEV with nivolumab for advanced cutaneous melanoma patients.
Jul 30 Advisory committee outcome Positive +107.0% Advisory committee voted that IGNYTE efficacy results were evaluable and clinically meaningful.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Replimune's recent announcements showed inconsistent price alignment, including a negative reaction to the August 6 FDA approval and a positive reaction to the July 30 advisory-committee update.

Key Terms

oncolytic immunotherapies
1 terms
oncolytic immunotherapies medical
"pioneering the development of novel oncolytic immunotherapies"
Oncolytic immunotherapies are treatments that use viruses or virus-like agents engineered to infect and destroy cancer cells while also waking up the immune system to attack tumors. Think of them as a Trojan horse that both breaks cancer’s defenses and calls in reinforcements; for investors, they matter because successful therapies can change standard cancer care, offer high commercial upside but come with steep scientific, regulatory and trial-stage risks that make outcomes binary and valuation-sensitive.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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WOBURN, Mass., Sept. 03, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a commercial stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced that members of the Replimune management team will present in a fireside chat at the Cantor Global Healthcare Conference on Thursday, September 10 at 9:10 AM ET.

A simultaneous webcast will be available in the Investors section of Replimune’s website at replimune.com. A replay will be available for 30 days following the conference.

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 TUDRIQEV (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.

Investor Inquiries

Chris Brinzey
ICR Healthcare
339.970.2843
chris.brinzey@icrhealthcare.com

Media Inquiries
Arleen Goldenberg
Replimune
917.548.1582
media@replimune.com


FAQ

When will Replimune (REPL) present at the Cantor Global Healthcare Conference?

Replimune is scheduled to present in a fireside chat at the Cantor Global Healthcare Conference on Thursday, September 10 at 9:10 AM ET.

How can investors access the Replimune (REPL) Cantor conference presentation?

A simultaneous webcast of Replimune’s fireside chat will be available in the Investors section of the company’s website at replimune.com.

Will a replay of Replimune’s Cantor Global Healthcare Conference webcast be available?

Yes. A replay of Replimune’s Cantor Global Healthcare Conference webcast will be available on the company’s website for 30 days following the conference.