CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
This prospectus supplement, the accompanying prospectus and the documents incorporated herein and therein by reference contain forward-looking statements made under the “safe harbor” provisions of the U.S. Private Securities Litigation Reform Act of 1995. These statements relate to future events or to our future financial performance and involve known and unknown risks, uncertainties and other factors which may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. The words “anticipate,” “assume,” “believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,” “goal,” “intend,” “may,” “might,” “objective,” “plan,” “potential,” “predict,” “project,” “positioned,” “seek,” “should,” “target,” “will,” “would,” or the negative of these terms or other similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words.
By their nature, forward-looking statements involve risks and uncertainties because they relate to events and depend on circumstances that may or may not occur in the future. We believe that these risks and uncertainties include, but are not limited to, those described in the “Risk Factors” sections of this prospectus supplement, the accompanying prospectus as well as in other documents incorporated by reference, which include, but are not limited to, the following:
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the initiation, timing, progress and results of our or our collaboration partners’ pre-clinical and clinical studies, and our research and development programs;
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our or our collaboration partners’ ability to advance our drug candidates into, and/or successfully complete, clinical studies;
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the timing of regulatory filings and the likelihood of favorable regulatory outcomes and approvals;
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regulatory developments in China, the United States and other countries;
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establishing and expanding our oncology drug sales team to support the marketing and sales of our approved drug candidates and the ability of our oncology drug sales team to develop and execute promotion and marketing activities;
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the timing, progress and results of our commercial launches, the rate and degree of market acceptance and potential market of any of our approved drug candidates;
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the pricing and reimbursement of our and our joint ventures’ products and our approved drug candidates;
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our ability to contract on commercially reasonable terms with contract research organizations, third-party suppliers and manufacturers;
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the scope of protection we are able to establish and maintain for intellectual property rights covering our or our joint ventures’ products and our drug candidates;
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the ability of third parties with whom we contract to successfully conduct, supervise and monitor clinical studies for our drug candidates;
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estimates of our expenses, future revenues, capital requirements and our needs for additional financing;
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our ability to obtain additional funding for our operations;
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the potential benefits of our collaborations and our ability to enter into future collaboration arrangements;
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the ability and willingness of our collaborators to actively pursue development activities under our collaboration agreements;
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our receipt of milestone or royalty payments, service payments and manufacturing costs pursuant to our strategic alliances with AstraZeneca AB (publ), or AstraZeneca, and Lilly (Shanghai) Management Company Limited, or Eli Lilly;
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our financial performance;
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our ability to attract and retain key scientific and management personnel;