Replimune Group Inc. reported research and development expenses of $57.9 million for the fiscal second quarter ended September 30, 2025, up from $43.4 million for the same period in 2024. The increase was mainly due to higher direct research costs related to the IGNYTE-3 confirmatory study and other study costs, as well as increased personnel-related expenses in preparation for a potential commercial launch of RP1. Cash, cash equivalents, and short-term investments totaled $323.6 million as of September 30, 2025, compared to $483.8 million as of March 31, 2025. The company announced the FDA accepted the BLA resubmission for RP1 for advanced melanoma, with a PDUFA target action date of April 10, 2026. Replimune expects its current cash position to fund operations into late Q4 2026, including potential commercialization of RP1 in skin cancers.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Replimune Group Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9570191-en) on November 06, 2025, and is solely responsible for the information contained therein.
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