FORWARD-LOOKING STATEMENTS
This prospectus and the information incorporated by reference in this prospectus contain certain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, or the Securities Act, and Section 21E of the Securities Exchange Act of 1934, as amended, the Exchange Act. All statements, other than statements of historical facts, contained in this prospectus and the information incorporated by reference herein, including statements regarding our strategy, future operations, future financial position, future revenues, projected costs, prospects, plans and objectives of management, are forward-looking statements. The words “anticipates”, “believes”, “could”, “estimates”, “expects”, “intends”, “may”, “plans”, “potential”, “predicts”, “projects”, “should”, “will”, “would” and the negative version of these words and other similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Such forward-looking statements are subject to various risks and uncertainties. Accordingly, there are or will be important factors that could cause actual outcomes or results to differ materially from those indicated in these statements.
The forward-looking statements in this prospectus and the documents incorporated by reference in the prospectus include, among other things, the statements about:
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the timing and conduct of our ongoing Phase 1 clinical trial of CT-0508 and our planned clinical trial utilizing CT-0508 in combination with pembrolizumab;
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the timing and conduct of our planned clinical trial of CT-0525 for solid tumors that overexpress HER2;
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the timing and conduct of our planned clinical trial of CT-1119 for advanced mesothelin-positive solid tumors;
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the timing and conduct of our planned clinical trial of CT-0729 for prostate-specific membrane antigen positive castrate resistant prostate cancer;
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our ability to replicate in later clinical trials positive results found in preclinical studies and early-stage clinical trials of our product candidates;
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our plans to conduct discovery and pre-clinical testing of the development of in vivo CAR-M therapeutics for up to twelve oncology targets, as well as multiple other targets and indications;
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our ability to successfully enroll patients in and complete clinical trials;
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our plans to conduct discovery and pre-clinical testing of other product candidates;
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our ability to realize the anticipated benefits of our research and development programs, strategic partnerships, research and licensing programs and academic and other collaborations;
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the timing of applying for and receiving, and our ability to maintain, marketing approvals from applicable regulatory authorities for our product candidates;
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our ability to obtain and maintain intellectual property protection and regulatory exclusivity for CT-0508 and any other product candidates we are developing or may develop in the future;
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acceptance of CT-0508 and any other product candidates, if and when approved, by patients, the medical community and third-party payors;
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our expectations regarding our ability to fund our operating expenses and capital expenditure requirements with our cash, cash equivalents and short-term investments;
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the potential advantages of our product candidates;
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our estimates regarding the potential market opportunity for our product candidates;
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our commercialization and manufacturing capabilities and strategy;
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the impact of COVID-19 on our business and operations;
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our estimates regarding expenses, future revenue, capital requirements and needs for additional financing;