SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS
This prospectus, together with any accompanying prospectus supplement, includes and incorporates by reference “forward-looking statements” within the meaning of the U.S. Private Securities Litigation Reform Act of 1995 and releases issued by the SEC and within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, which statements involve substantial risks and uncertainties. Forward-looking statements generally relate to future events or our future financial or operating performance. All statements other than statements of historical fact are “forward-looking statements” for purposes of this prospectus. In some cases, you can identify forward-looking statements because they contain words such as “may,” “will,” “would,” “should,” “could,” “expect,” “plan,” “anticipate,” “intend,” “target,” “project,” “contemplate,” “believe,” “estimate,” “predict,” “seek,” “potential,” “ongoing,” “goal,” or “continue,” or the negative of these words or other similar terms or expressions that concern our expectations, strategy, plans or intentions. Forward-looking statements contained in this prospectus include, but are not limited to, statements about:
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how long we expect to maintain liquidity to fund our planned level of operations and our ability to obtain additional funds for our operations;
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the development of our drug and vaccine candidates, including when we expect to undertake, initiate and complete clinical trials of our drug and vaccine candidates;
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the expectation, plans, projections, initiation, timing, progress and results of our research and development programs, preclinical studies, any clinical trials, compassionate uses, Investigational New Drug (“IND”) filings, Clinical Trial Application (“CTA”) filings, New Drug Application (“NDA”) filings, Biologics License Application (“BLA”), and other regulatory submissions;
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regulatory developments involving products and our facilities, including the ability to obtain regulatory approvals or otherwise bring products to market;
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the regulatory status of our drug and vaccine candidates, including our ability to obtain and maintain orphan drug, rare pediatric and Regenerative Medicine Advanced Therapy (“RMAT”) designations for our lead product candidate, CAP-1002;
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our use of clinical research centers, third party manufacturers and other contractors;
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our ability to find collaborative partners for research, development and commercialization of potential products and retain commercial rights for our product candidates in the collaborations;
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our ability to manufacture products for clinical and commercial use;
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our ability to procure materials necessary for the manufacture of our product candidates;
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our ability to protect our patents and other intellectual property;
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our ability to raise additional financing and the terms of any additional financing;
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our ability to market any of our products;
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the implementation of our business model and strategic plans for our business, technologies and product candidates;
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our estimates of our expenses, ongoing losses, future revenue, future reimbursement prices for any commercial products, and capital requirements;
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the impact of taxes on our business;
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our ability to compete against other companies and research institutions;
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our ability to expand our operations internationally;
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the effect of potential strategic transactions on our business;
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acceptance of our products by doctors, patients or payors and the availability of reimbursement for our product candidates;
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our ability to attract and retain key personnel; and