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Replimune announces that a brand new abstract from the primary analysis of the IGNYTE clinical trial has been selected for oral presentation at the European Society for Medical Oncology (ESMO) 2024 Congress





Replimune Group (NASDAQ: REPL) announced that a current abstract containing the primary analysis of the IGNYTE clinical trial has been submitted for oral presentation at the Congress of the European Society for Medical Oncology (ESMO) 2024. The presentation entitled “Primary efficacy, safety and survival data from the enrollment cohort of patients with melanoma who have failed anti-PD-1 treatments from the IGNYTE clinical trial of RP1 in combination with nivolumab” will be given by Dr. Caroline Robert of the Gustave Roussy Cancer Center on 15 September 2024This presentation is part of the Melanoma and Other Skin Tumors Mini Lecture Session and highlights Replimune's progress in developing novel oncolytic immunotherapies.

Replimune Group (NASDAQ: REPL) announced a high-stakes summary, presented the lead analysis of the IGNYTE study and was selected for an oral presentation Congress of the Società Europea di Oncologia Medica (ESMO) 2024. The presentation was: “The first effective, secured and improved data for patients with melanoma who have suffered anti-PD-1 treatment during the IGNYTE study with RP1 combination with nivolumab,” said Dr. ssa Caroline Robert of Gustave Roussy Cancer Center il 15 September 2024This presentation was made in part during the oral mini-session on Melanoma and other skin tumors, Replimune evidence and progress in developing new oncology immunotherapies.

Replimune Group (NASDAQ: REPL) announced that IGNYTE resumed a few days ago and selected the main analysis of the IGNYTE clinic for an oral presentation on site Congress of the Sociedad Europea de Oncología Médica (ESMO) 2024. The presentation entitled “Priority efficacy, safety and surveillance data of the group of patients with melanoma damaged in the anti-PD-1 treatment of the Ensay Clinic IGNYTE in combination with RP1 with nivolumab” was organized by the Dr. Caroline Robert del Gustave Roussy Cancer Center el 15 September 2024This presentation is part of the Mini-Oral session on Melanoma and other skin tumors, following the progress of Replimune and the development of new oncology immunotherapies.

Replimune Group (NASDAQ: REPL) was founded by IGNYTE and has been active in the industry since 2010 2024: New Year of the Year 2024 of the European Parliament (ESMO).발표했다. “RP1 and nivolumab are an anti-PD-1 antibiotic-antibiotic-antibiotic. 및 생존 데이터'라는 제목의 발표는 15 September 2024 Gustave Roussy by Dr. Caroline Robert by Dr. CarolineRobert. 이 발표는 멜라노마 및 새로운 온콜리틱 면역요법 개발에 대한 Replimune의 진행 상황을 강조한다.

Replimune Group (NASDAQ: REPL) announced a last minute summary in which the main analysis of the IGNYTE clinic was selected for an oral presentation to you Congress of the Société Européenne d'Oncologie Médicale (ESMO) 2024. The presentation entitled “Efficacy, safety and initial screening results of the melanoma cohort confirmed by the IGNYTE clinic’s anti-PD-1 treatment with RP1 in association with nivolumab”, effective sera by Dr . Caroline Robert du Gustave Roussy Cancer Center le 15 September 2024This presentation concluded the oral mini-session on melanoma and other skin tumors and highlighted the advanced Replimune processes in the development of new oncolytic immunotherapies.

Replimune Group (NASDAQ: REPL) announced that a key abstract presenting the primary analysis of the IGNYTE study has been submitted for oral presentation at the European Congress of Medical Oncology (ESMO) 2024 The presentation entitled “Primary efficacy, safety and survival data from the registry-based cohort of patients with anti-PD-1 failed melanoma from the IGNYTE study of RP1 in combination with nivolumab” will be given by Dr. Caroline Robert from the Gustave Roussy Cancer Center at 15 September 2024 This presentation is part of the mini-oral session on melanoma and other skin tumors and highlights Replimune's progress in developing novel oncolytic immunotherapies.

Positive


  • Current abstract selected for oral presentation at ESMO Congress 2024

  • Presentation focuses on primary analysis of the IGNYTE clinical trial

  • The study involves patients with melanoma who no longer respond to anti-PD-1 therapy, meaning there is a significant unmet medical need











WOBURN, Mass., Aug. 22, 2024 (GLOBE NEWSWIRE) — Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company pioneering a new class of oncolytic immunotherapies, today announced that a late-breaking abstract containing the primary analysis from the IGNYTE clinical trial has been selected for an oral presentation at the 2024 European Society for Medical Oncology (ESMO) Congress, to be held in Barcelona, ​​September 13-17, 2024.

Presentation details:

Title: Primary efficacy, safety and survival data from the enrollment cohort of patients with melanoma who have failed anti-PD-1 treatments from the IGNYTE clinical trial of RP1 in combination with nivolumab
Title of the presentation session: Mini Oral Session – Melanoma and other skin tumors
Presentation number: LBA46
Date and time: Sunday, 15 September 2024, 15:45 – 15:50 CEST
Speakers: Caroline Robert, MD, PhD, Gustave Roussy Cancer Center

About RP1
RP1 (vusolimogene or parepvec) is Replimune's lead product candidate and is based on a proprietary strain of herpes simplex virus that has been genetically modified and encoded with a fusogenic protein (GALV-GP R) and GM-CSF, which are designed to maximize the tumoricidal effect, the immunogenicity of tumor cell death and the activation of a systemic anti-tumor immune response.

About Replimune
Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the goal of revolutionizing cancer treatment by developing a novel portfolio of oncolytic immunotherapies. Replimune's proprietary RPx platform is based on a potent HSV-1 backbone designed to maximize immunogenic cell death and induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct, selective virus-mediated tumor killing resulting in the release of tumor-related antigens and alteration of the tumor microenvironment to elicit a potent and durable systemic response. The RPx product candidates are expected to act synergistically with most established and experimental cancer treatment modalities, resulting in versatility that allows them to be developed alone or in combination with a variety of other treatment options. For more information, visit www.replimune.com.

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 design and advancement of our clinical trials, the timing and adequacy of the results of our clinical trials to support potential approval of our product candidates, our goals for developing and commercializing our product candidates, patient enrollment in our existing and planned clinical trials and the timing thereof, and other statements identified by words such as “may,” “expects,” “intends,” “may,” “plans,” “potential,” “should,” “will,” “would” or similar expressions and the negative of these terms. Forward-looking statements are not promises or guarantees of future performance and are subject to a number of risks and uncertainties, many of which are beyond our control and which could cause actual results to differ materially from those anticipated in such forward-looking statements. These factors include risks related to our limited operating history, our ability to achieve positive clinical trial results for our product candidates, the cost and timing of operating our in-house manufacturing facility, the timing and scope of regulatory approvals, the availability of combination therapies required to conduct our clinical trials, changes in laws and regulations to which we are subject, competitive pressures, our ability to identify additional product candidates, political and global macro factors, including the impact of the coronavirus as a global pandemic and related public health issues and the political and military conflicts between Russia and Ukraine and between Israel and Hamas, and other risks that 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 may differ materially from those described or implied by such forward-looking statements. Forward-looking statements speak only as of the date they are made, and except as required by law, we undertake no obligation to update or revise these forward-looking statements.

Inquiries from investors
Chris Brinzey
ICR Westwick
339.970.2843
[email protected]

Media inquiries
Arleen Goldenberg
Replimune
917.548.1582
[email protected]









Frequently Asked Questions



What is the IGNYTE clinical trial that Replimune (REPL) is presenting at ESMO 2024?

The IGNYTE clinical trial is evaluating RP1 in combination with nivolumab in patients with melanoma who have failed anti-PD-1. The primary analysis of this trial, including efficacy, safety and survival data, will be presented at ESMO 2024.


When and where will Replimune (REPL) present the results of the IGNYTE study at ESMO 2024?

Replimune will present the results of the IGNYTE study on September 15, 2024 from 15:45 – 15:50 CEST during the ESMO Congress 2024 in Barcelona.


Who will present the IGNYTE study results of Replimune (REPL) at ESMO 2024?

Dr. Caroline Robert from the Gustave Roussy Cancer Center will present the results of the IGNYTE study at ESMO 2024.


What type of cancer is Replimune's (REPL) IGNYTE study, presented at ESMO 2024, targeting?

The IGNYTE trial, presented at ESMO 2024, targets anti-PD-1-failed melanoma, a type of skin cancer that has failed previous anti-PD-1 therapies.