Recent Updates
Recently added Catalysts
REPL Positive Sentiment

Replimune to Present at the Cantor Global Healthcare Conference 2026

Key Takeaway: Replimune Group, Inc. will present at the Cantor Global Healthcare Conference on September 10, 2026. The management team will engage in a fireside chat, which will also be available via webcast. Replimune focuses on developing oncolytic immunotherapies, with its product TUDRIQEV already approved for advanced melanoma treatment.

Market Sentiment Analysis

POSITIVE FACTORS

  • Replimune is pioneering novel oncolytic immunotherapies.
  • The company has a commercially available product approved by the FDA.
  • The upcoming presentation at a major healthcare conference indicates strong investor interest.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+840%
120-day peak, hindsight
Typical move
25.1%
average across 6 past catalysts
Cash runway
~7 mo
Medium dilution risk
Lead asset
RP1
Phase 2 · Non-Small Cell Lung Cancer (NSCLC)

Full Press Release Details

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

Frequently Asked Questions

When will Replimune present at the conference?

Replimune will present on September 10, 2026, at 9:10 AM ET.

Where can I watch the Replimune presentation?

The presentation will be available via webcast on Replimune's website.

What is TUDRIQEV?

TUDRIQEV is Replimune's first FDA-approved product for advanced melanoma.

What is the focus of Replimune?

Replimune focuses on developing novel oncolytic immunotherapies for cancer treatment.

Last updated: Sep 3, 2026