CAUTIONARY NOTE REGARDING FORWARD-LOOKING INFORMATION
This Prospectus and the documents incorporated by reference herein and therein contain “forward-looking information” under applicable Canadian securities legislation and “forward-looking statements” within the meaning of the United States Private Securities Litigation Reform Act of 1995, as amended (collectively, “forward-looking information”). Except for statements of historical fact relating to the Corporation, information contained or incorporated by reference herein constitutes forward-looking information, including, but not limited to, any information as to the Corporation’s strategy, plans or future performance. Forward-looking information is characterized by words such as “seek”, “anticipate”, “plan”, “continue”, “estimate”, “expect”, “may”, “will”, “project”, “predict”, “potential”, “targeting”, “intend”, “could”, “might”, “would”, “should”, “believe”, “objective”, “ongoing”, “imply”, “assumes”, “goal”, “likely” and similar references to future periods or the negatives of these words and expressions. In particular, forward-looking statements included or incorporated by reference in this Prospectus include, without limitation, statements with respect to:
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the Corporation’s ability to raise the financing necessary for its operations;
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the duration and effects of COVID-19 and any other pandemics on the Corporation’s workforce, business, operations and financial condition;
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the Corporation’s expected future loss and accumulated deficit levels;
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the Corporation’s projected financial position and estimated cash burn rate;
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the Corporation’s requirements for, and the ability to obtain, future funding on favorable terms or at all;
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the Corporation’s projections for development plans and progress of each of its product candidates, particularly with respect to the timely and successful completion of studies and trials and availability of results from such studies and trials;
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the Corporation’s expectations about the safety and efficacy of its product candidates;
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the Corporation’s expectations regarding its ability to arrange for and scale up the manufacturing of product candidates;
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the Corporation’s expectations regarding the progress, and the successful and timely completion, of the various stages of the regulatory approval process;
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the Corporation’s expectations about whether various clinical and regulatory milestones will be achieved;
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the Corporation’s expectations about the timing of achieving milestones and the cost of its development programs;
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the Corporation’s plans to market, sell and distribute its product candidates;
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the Corporation’s expectations regarding the acceptance of its product candidates by the market;
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the Corporation’s ability to retain and access appropriate staff, management and expert advisers;
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the Corporation’s ability to strictly comply with federal, state, local and regulatory agencies in the United States and other jurisdictions in which the Corporation operates, including Australia, Switzerland and the Netherlands;
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the Corporation’s expectation that jurisdictions in which the Corporation operates, including Australia, Switzerland and the Netherlands, have similar regulatory frameworks as the United States;
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the Corporation’s expectations of the costs and timing to reach commercial production of drug products;
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the Corporation’s ability to secure strategic partnerships with academic research institutions and larger pharmaceutical and biotechnology companies;
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the Corporation’s continuation of strategic collaborations;