Press Releases September 3, 2026 08:00 AM

Replimune to Present at the Cantor Global Healthcare Conference 2026

Replimune Group to Present at Cantor Global Healthcare Conference 2026

By Derek Hwang
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REPL

Replimune Group, a biotechnology company specializing in oncolytic immunotherapies, announced that its management team will present at the Cantor Global Healthcare Conference on September 10, 2026. The company highlighted its first commercially approved product, TUDRIQEV, for advanced melanoma, and its proprietary RPx platform aiming to enhance cancer treatment through immunotherapy.

Replimune to Present at the Cantor Global Healthcare Conference 2026
REPL
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Key Points

  • Replimune will host a fireside chat at a major healthcare conference, increasing visibility among investors and industry peers.
  • Its first product, TUDRIQEV, is FDA-approved under accelerated approval for advanced melanoma treatment, involving combination immunotherapy.
  • The RPx platform is designed to maximize immunogenic cell death and augment systemic anti-tumor immune response, offering potential versatility across cancer therapies.

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
[email protected]

Media Inquiries
Arleen Goldenberg
Replimune
917.548.1582
[email protected]


Risks

  • The company's therapy is currently approved under accelerated approval, which may require further confirmatory trials to maintain full regulatory approval, posing regulatory risks.
  • The success of oncolytic immunotherapies depends on clinical outcomes and adoption by medical practitioners, which introduces clinical and market adoption risks.
  • Competition in the immunotherapy and cancer treatment sector is intense, which may impact market share and future growth prospects.

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