Replimune reported their Q4 2022 financial results and corporate update, ending the fiscal year in a strong position. They are maintaining guidance to complete enrollment into the CERPASS clinical trial in CSCC mid-year and to release top line data in early 2023. Initial directional data from the IGNYTE clinical trial in anti-PD1 failed melanoma is expected in late 2022.
Enrollment in the CERPASS clinical trial with RP1 in cutaneous squamous cell carcinoma (CSCC) is expected to be completed in mid-year 2022; top line data expected Q1 2023.
Directional data from the first 75 patents with 6 months follow up from the IGNYTE clinical trial with RP1 in anti-PD1 failed melanoma is expected in late 2022.
Phase 2 development plan for RP2/RP3 in HCC, CRC and SCCHN announced.
Existing cash and cash equivalents and short-term investments will fund operating expenses and capital expenditure requirements into the second half of 2024.
Replimune believes that existing cash and cash equivalents and short-term investments will fund operating expenses and capital expenditure requirements into the second half of 2024, excluding any confirmatory trial required by the FDA or other regulatory body.