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, aiming to establish this as a key immune-based cancer treatment alongside checkpoint blockade.
Proprietary RPx platform uses engineered HSV-1 viruses to induce local and systemic anti-tumor immune responses, with three product candidates: RP1, RP2, and RP3.
Lead candidate RP1 is in advanced clinical trials, including a Phase 2 registration-directed cohort for anti-PD1 failed melanoma and additional studies in non-melanoma skin cancers and transplant recipients.
RP2 and RP3 are engineered for broader tumor targeting and enhanced immune activation, with RP2 advancing toward a registration-directed study in metastatic uveal melanoma.
Financial performance and metrics
Raised approximately $100 million in gross proceeds from a private placement in June 2024, selling 5,668,937 shares and pre-funded warrants for 5,669,578 shares.
As of June 30, 2024, 68,309,968 shares of common stock were outstanding, excluding options, restricted stock units, and additional warrants.
Use of proceeds and capital allocation
Will not receive proceeds from resale of shares by selling stockholders; may receive up to $5,669 from nominal exercise of pre-funded warrants.
Any proceeds from warrant exercises will be used for working capital and general corporate purposes.
Latest events from Replimune Group
- 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 - Up to $250M in securities, including $100M ATM, to fund late-stage cancer immunotherapy pipeline.REPL
Registration Filing16 Dec 2025