Statements made in, or accessible through this page, regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Such statements include, but are not limited to, statements regarding Replimune ability to successfully initiate and complete clinical trials and development programs, the expected timing for reporting of top-line data, Replimune ability to obtain regulatory approval, market penetration and acceptance of any of it’s products and the initiation of clinical studies. Risks that contribute to the uncertain nature of the forward-looking statements include: Replimune future preclinical studies and clinical trials may not be successful; changes in regulatory requirements in the United States and foreign countries may prevent or significantly delay regulatory approval of Replimune products; Replimune may change its plans to develop and commercialize its product candidates; the FDA may not agree with Replimune interpretation of the data from clinical trials; Replimune may decide, or the FDA may require Replimune, to conduct additional clinical trials or to modify Replimune clinical trials; Replimune may experience delays in the commencement, enrollment, completion or analysis of clinical testing for its product candidates, or significant issues regarding the adequacy of its clinical trial designs or the execution of its clinical trials, which could result in increased costs and delays, or limit Replimune ability to obtain regulatory approval; the third parties with whom Replimune has partnered with for the development of its products and upon whom Replimune relies to conduct its clinical trials and manufacture its product candidates may not perform as expected; Replimune may not receive regulatory approval for its products or be successfully commercialized; unexpected adverse side effects or inadequate therapeutic efficacy of any of its products could delay or prevent regulatory approval or commercialization; Replimune may be unable to obtain and maintain intellectual property protection for its product candidates; the loss of key scientific or management personnel; Replimune ability to obtain additional financing; and the accuracy of Replimune estimates regarding expenses, future revenues and capital requirements. All forward-looking statements contained in this presentation speak only as of the date on which they were made. Replimune undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.
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