FORWARD-LOOKING STATEMENTS
This prospectus supplement and the accompanying prospectus, including the documents incorporated herein and therein by reference, contain forward-looking statements that involve substantial risks and uncertainties. All statements other than statements of historical facts contained in this prospectus supplement and the accompanying prospectus, including the documents that are incorporated herein and therein by reference, including statements regarding our strategy, future operations, future financial position, future revenue, projected costs, prospects, plans, objectives of management and expected growth, are forward-looking statements. These statements involve known and unknown risks, uncertainties and other important factors that 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,” “believe,” “expect,” “intend,” “may,” “plan,” “predict,” “project,” “target,” “potential,” “will,” “would,” “could,” “should,” “continue” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. These forward-looking statements include, among other things, statements about:
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our ability to successfully commercialize our approved medicines and to obtain approvals in additional indications and territories for our medicines;
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our ability to successfully develop and commercialize our in-licensed medicines and drug candidates and any other medicines and drug candidates we may in-license;
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our ability to further develop sales and marketing capabilities and launch and commercialize new medicines, if approved;
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our ability to maintain and expand regulatory approvals for our medicines and drug candidates, if approved;
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the pricing and reimbursement of our medicines and drug candidates, if approved; the initiation, timing, progress and results of our preclinical studies and clinical trials and our research and development programs;
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our ability to advance our drug candidates into, and successfully complete, clinical trials and obtain regulatory approvals;
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our reliance on the success of our clinical stage drug candidates;
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our plans, expected milestones and the timing or likelihood of regulatory filings and approvals;
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the implementation of our business model, strategic plans for our business, medicines, drug candidates and technology;
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the scope of protection we (or our licensors) are able to establish and maintain for intellectual property rights covering our medicines, drug candidates and technology;
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our ability to operate our business without infringing, misappropriating or otherwise violating the intellectual property rights and proprietary technology of third parties;
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costs associated with enforcing or defending against intellectual property infringement, misappropriation or violation, product liability and other claims;
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the regulatory environment and regulatory developments in the United States, China, the United Kingdom, the European Union (“EU”) and other jurisdictions in which we operate;
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the accuracy of our estimates regarding expenses, revenues, capital requirements and our need for additional financing;
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the potential benefits of strategic collaboration and licensing agreements and our ability to enter into strategic arrangements;
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our ability to maintain and establish collaborations or licensing agreements;
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our reliance on third parties to conduct drug development, manufacturing and other services;