Replimune Announces Financial Results for Fiscal Q2 2026 and Shares Corporate Developments
Financial Results: Replimune Group reported a net loss of $83.1 million for the fiscal second quarter ended September 30, 2025, with cash reserves decreasing to $323.6 million, expected to fund operations into late 2026.
FDA Update: The FDA accepted the resubmission of Replimune's Biologics License Application (BLA) for RP1, targeting advanced melanoma, with a decision expected by April 10, 2026.
Clinical Trials: Ongoing trials for RP1 and RP2 are assessing their effectiveness in various cancers, including advanced melanoma and metastatic uveal melanoma, with promising early results reported at recent conferences.
Upcoming Events: Replimune will present new clinical data at the Society for Immunotherapy of Cancer (SITC) Annual Meeting, highlighting the potential of RP1 in overcoming resistance to immune checkpoint blockade.
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