CAUTOINARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
This prospectus supplement, the accompany prospectus, including the documents incorporated by reference herein and therein, and any free writing prospectus that we have authorized for use in connection with this offering contain forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 concerning our business, operations and financial performance and condition, as well as our plans, objectives and expectations for our business operations and financial performance and condition. Any statements contained herein that are not statements of historical facts may be deemed to be forward-looking statements. In some cases, you can identify forward-looking statements by terminology such as “aim,” “anticipate,” “assume,” “believe,” “contemplate,” “continue,” “could,” “due,” “estimate,” “expect,” “goal,” “intend,” “may,” “objective,” “plan,” “predict,” “project,” “potential,” “positioned,” “seek,” “should,” “target,” “will,” “would,” and other similar expressions that are predictions or that indicate future events and future trends, or the negative of these terms or other comparable terminology. These forward-looking statements include, but are not limited to, statements about:
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our expectations and beliefs regarding the potential benefits of our product candidates;
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our expectations regarding the clinical effectiveness of our product candidates and utility of our biomarker data;
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the anticipated timing, costs and conduct of our ongoing and planned clinical trials for soquelitinib, ciforadenant and mupadolimab and planned preclinical studies and clinical trials for other product candidates in our development programs;
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the scope and design of our planned clinical trials, including but not limited to target patient enrollment numbers;
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our ability to develop, acquire and advance product candidates into, and successfully complete, clinical trials;
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the timing of the completion of our ongoing and planned clinical trials of soquelitinib, ciforadenant and mupadolimab and the timing and availability of clinical data from such clinical trials;
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clinical and regulatory development plans with respect to soquelitinib, ciforadenant and mupadolimab, and our other product candidates;
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our ability to commercialize soquelitinib, ciforadenant and mupadolimab and our other product candidates, if approved;
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our commercialization, marketing and manufacturing capabilities and strategy;
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the pricing and reimbursement of our product candidates, if approved;
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our strategy to protect, establish and maintain our proprietary technology and intellectual property rights covering our product candidates, including the projected terms of patent protection;
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our ability to establish and maintain collaborations and retain commercial rights for our product candidates in such collaborations;
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the potential benefits of strategic collaborations, including our collaboration with Angel Pharmaceuticals, and our ability to enter into strategic arrangements;
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developments and projections relating to our competitors and our industry, including competing therapies and our beliefs regarding our competitive advantage;
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our estimates regarding the effect of certain changes in tax law and uncertainty as to how some of those changes may be applied;
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our estimates regarding expenses, future revenue, capital requirements and needs for additional financing;
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our estimates of the sufficiency of our cash, cash equivalents and marketable securities;
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our financial performance; and
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our intended use of proceeds from this offering, if any.