Press Releases

06-29 Replimune Reports Fiscal Fourth Quarter and Year End 2026 Financial Results and Provides Corporate Update AQ
06-26 Replimune Announces FDA Acceptance of RP1 Biologics License Application Resubmission for Advanced Melanoma AQ
05-31 Replimune Presents Final First-in-Human Data for RP2 in Advanced Solid Tumors During Oral Presentation at the 2026 American Society of Clinical Oncology Annual Meeting AQ
05-30 Replimune Presents 3-Year Landmark Overall Survival Analysis from IGNYTE Clinical Trial During Oral Presentation at the 2026 American Society of Clinical Oncology Annual Meeting GL
05-29 Replimune Announces Planned RP1 BLA Resubmission Following Productive Discussion with FDA AQ
04-27 Replimune to Present at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting AQ
04-23 Replimune : RP1 + Nivolumab in Patients with NMSC at EADO 2026 PU
04-23 Replimune : RP1 + Nivolumab in Patients with Anti–PD-1–Failed Melanoma at EADO 2026 PU
04-13 Replimune Receives Complete Response Letter from the FDA for RP1 Biologics License Application for the Treatment of Advanced Melanoma AQ
04-10 Replimune Receives Complete Response Letter from the FDA for RP1 Biologics License Application for the Treatment of Advanced Melanoma AQ
03-02 Replimune to Present at Two Upcoming Investor Conferences AQ
02-03 Replimune Reports Fiscal Third Quarter 2026 Financial Results and Provides Corporate Update AQ
01-14 Replimune : JP Morgan Healthcare Conference 2026 Presentation PU
12-18 Replimune to Present at the 44th Annual J.P. Morgan Healthcare Conference AQ
11-07 Replimune : IGNYTE Trial Biomarker and Updated Clinical Data Presentation at SITC 2025 PU
11-07 Replimune Presents Late-Breaking Abstract and Additional Posters on RP1 at 40th Annual Meeting of the Society for the Immunotherapy of Cancer (SITC 2025) AQ
11-07 Replimune : RP1 + Nivolumab in Patients with Advanced Anti–PD-1–Failed Melanoma at SITC 2025 PU
11-07 Replimune : RP1 + Nivolumab in Patients with and without prior BRAF-Directed Therapy at SITC 2025 PU
11-06 Replimune Reports Fiscal Second Quarter 2026 Financial Results and Provides Corporate Update AQ
20/10/25 Replimune Announces FDA Acceptance of BLA Resubmission of RP1 for the Treatment of Advanced Melanoma AQ
19/10/25 Replimune Highlights Acral Melanoma Data for RP1 plus Nivolumab at the ESMO Congress 2025 AQ
18/10/25 Replimune : RP1 + Nivolumab in Patients with NMSC at ESMO 2025 PU
18/10/25 Replimune : RP1 + Nivolumab in Patients with Advanced Anti–PD-1–Failed Acral Melanoma at ESMO 2025 PU
22/09/25 Replimune Group, Inc. Securities Fraud Class Action Lawsuit Pending: Contact The Gross Law Firm Before September 22, 2025 to Discuss Your Rights - REPL PR
20/09/25 Replimune (REPL) Shares Tank 45% After Company Says No Pathway Identified For Lead Drug RP1, Securities Class Action Pending - Hagens Berman PR
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