Replimune Group (REPL) Registration Filing summary
Event summary combining transcript, slides, and related documents.
Registration Filing summary
16 Dec, 2025Company overview and business model
Clinical-stage biotechnology company focused on oncolytic immunotherapy for cancer, leveraging a proprietary RPx platform based on engineered herpes simplex virus 1 to activate immune responses against tumors.
Pipeline includes three product candidates: RP1 (lead), RP2, and RP3, targeting both skin and non-skin cancers, with multiple ongoing clinical trials in collaboration with major partners.
RP1 is being developed as monotherapy and in combination with anti-PD-1 therapy, with a major focus on advanced melanoma and non-melanoma skin cancers.
RP2 and RP3 are engineered to enhance immune responses and address additional tumor types, including those less responsive to immunotherapy.
Financial performance and metrics
Identified as a "smaller reporting company" with less than $250 million in market value of shares held by non-affiliates as of the last business day of the second fiscal quarter.
77,085,024 shares of common stock outstanding as of March 31, 2025, with additional shares reserved for options, warrants, and incentive plans.
Use of proceeds and capital allocation
Will not receive proceeds from the sale of shares by selling stockholders; may receive nominal proceeds from exercise of pre-funded warrants, intended for working capital and general corporate purposes.
Latest events from Replimune Group
- Registering 25.1M shares for resale, the company faces regulatory and financial uncertainty.REPL
Registration filing24 Jul 2026 - Stockholders will vote on auditor ratification, executive pay, and doubling authorized shares.REPL
Proxy filing13 Jul 2026 - Directors were elected, key proposals passed except the incentive plan amendment.REPL
AGM 20259 Jul 2026 - RP1 plus nivolumab achieved a 33.6% ORR and durable responses in anti-PD1 failed melanoma.REPL
Study Result9 Jul 2026 - RP1 shows 34% response in anti-PD-1 failed melanoma, with global launch and expansion planned.REPL
43rd Annual J.P. Morgan Healthcare Conference 20258 Jul 2026 - FDA accepted RP1 BLA resubmission; cash funds operations into 2027; strong clinical results.REPL
Q4 202629 Jun 2026 - Awaiting April 10th PDUFA for RP1, with commercial launch readiness and robust pipeline progress.REPL
Leerink Global Healthcare Conference 20269 Mar 2026 - Net loss rose to $70.9M, FDA review of RP1 advances, and cash runway extends into Q1 2027.REPL
Q3 20263 Feb 2026 - RP1 and RP2 show strong efficacy in tough cancers, with regulatory and commercial progress ongoing.REPL
Goldman Sachs 45th Annual Global Healthcare Conference1 Feb 2026 - Oncolytic immunotherapy nears launch with strong efficacy and broad pipeline expansion.REPL
44th Annual J.P. Morgan Healthcare Conference14 Jan 2026