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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 Auspex’s ability to successfully complete its ongoing clinical trials and development programs, the expected timing for reporting of top-line data, Auspex’s ability to obtain regulatory approval, market penetration and acceptance of any of its products and the initiation of clinical studies. Risks that contribute to the uncertain nature of the forward-looking statements include: Auspex’s 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 Auspex’s products; Auspex may change its plans to develop and commercialize its product candidates; the FDA may not agree with Auspex’s interpretation of the data from clinical trials; Auspex may decide, or the FDA may require Auspex, to conduct additional clinical trials or to modify Auspex’s ongoing clinical trials; Auspex 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 Auspex’s ability to obtain regulatory approval; the third parties with whom Auspex has partnered with for the development of its products and upon whom Auspex relies to conduct its clinical trials and manufacture its product candidates may not perform as expected; Auspex 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; Auspex’s may be unable to obtain and maintain intellectual property protection for its product candidates; the loss of key scientific or management personnel; Auspex’s ability to obtain additional financing; and the accuracy of Auspex’s 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. Auspex 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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All Auspex brand and product names are trademarks or registered trademarks of Auspex Pharmaceuticals, Inc. in the United States and other countries. The following, which appear on this web site, are registered or other trademarks owned by the following companies: XENAZINE® (Lundbeck); Brilinta® (AstraZeneca), Effexor™ (Pfizer).