Hill Emily Luisa sold $132K of REPL

Replimune Group reported no revenue in Q3 2026, with net loss narrowing to $57.1M from $83.1M a year earlier. Diluted loss per share was $0.54. The FDA approved TUDRIQEV in August, with U.S. sales starting in October. Over 15 institutions began treatments by October 23. The company is conducting clinical trials for TUDRIQEV and RP2.

Replimune reported a net loss of $57.1M for Q2 2027, down from $83.1M a year earlier. Cash reserves were $307.8M. R&D and operating expenses decreased. TUDRIQEV, for advanced melanoma, launched commercially in the U.S. in October, with over 15 institutions prescribing it. The company is engaging with priority accounts and advancing clinical trials.

Replimune Group, Inc. (REPL) filed an SEC Form 8-K — Results of Operations and Financial Condition. Exhibit 99.1 Replimune Reports Fiscal Second Quarter 2027 Financial Results and Provides Corporate Update TUDRIQEV first delivered to patients for advanced melanoma on October 6th More than 15 institutions have prescribed TUDRIQEV Management will host a webcast today at 8:00 a.m.

Replimune Group Inc. (REPL) announced the U.S. commercial launch of TUDRIQEV, a melanoma therapy for advanced cutaneous melanoma patients who progressed on PD-1-blocking treatments. The FDA granted accelerated approval based on a 24.2% objective response rate in trials. The company estimates 105,000 new U.S. melanoma cases in 2025. Continued approval depends on confirmatory trial results.

Replimune Group, Inc. (REPL) has begun U.S. sales of TUDRIQEV for advanced melanoma patients after PD-1 therapy, under accelerated approval. This marks the company's first commercial launch, transitioning from clinical-stage to revenue generation. Successful adoption could drive significant revenue growth, according to the company.

Replimune Group, Inc. (REPL) announced that TUDRIQEV™, a treatment for advanced melanoma, is now available in the U.S. The therapy, approved under accelerated approval, is indicated for adult patients who have progressed with PD-1-blocking antibody regimens. TUDRIQEV achieved a 24.2% objective response rate in clinical trials, with a median duration of 14.1 months. The company also launched a patient support program to assist with access and reimbursement.