Replimune Group, Inc. announced its financial results for the fiscal third quarter ended December 31, 2024, and provided a corporate update on February 12, 2025. The company highlighted significant regulatory milestones for RP1 in anti-PD-1 failed melanoma, including its Priority Review status and a PDUFA date of July 22, 2025, set by the FDA.
CEO Sushil Patel stated that Replimune's efforts are focused on ensuring a successful commercial launch of RP1 upon potential approval. The commercial strategy is designed to effectively deliver intratumoral therapy, based on a deep understanding of the patient population and prescriber landscape.
The company reported holding over $500 million in cash, indicating it is well-capitalized to execute its plans. Replimune expressed anticipation for providing further updates as it transitions towards becoming a commercial-stage company.
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