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Innovation In Ophthalmics Corporate Overview August 2020
August 2020NOT FOR PROMOTIONAL USE
Disclaimers and Notices
This presentation contains forward -looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 , that involve substantial risks and uncertainties,
including statements regarding INVELTYS® and its commercial progress, the Company's lead product candidate, EYSUVISTM, for the short -term relief of the signs and symptoms of
dry eye disease, including expectations regarding timing of FDA review of the New Drug Application (NDA) and potential launch byyear -end 2020, the market for EYSUVIS,
including the potential for EYSUVIS to be suitable for the vast majority of patients with dry eye disease, the Company’s plan toexpand its commercial sales force and the
Company’s expectations regarding its use of cash, cash runway and projected revenues. All statements, other than statements o f historical facts, contained in this presentation,
including statements regarding the Company’s strategy, future operations, future financial position, future revenue, projecte d costs, prospects, plans and objectives of
management, are forward -looking statements. The words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “inten d,” “may,” “plan,” “potential,” “predict,”
“project,” “should,” “target,” “will,” “would,” and similar expressions are intended to identify forward -looking statements, alt hough not all forward -looking statements contain
these identifying words. The Company may not actually achieve the plans, intentions or expectations disclosed in its forward -looking statements, and you should not place undue
reliance on such forward -looking statements. Actual results or events could differ materially from the plans, intentions and exp ectations disclosed in the forward -looking
statements as a result of various risks and uncertainties including, but not limited to: the impact of extraordinary external events, such as the current pandemic health event
resulting from the novel coronavirus (COVID -19), and their collateral consequences, including disruption of the activities of ou r sales force and the market for INVELTYS and any
delay in timing of regulatory review of the NDA for EYSUVIS; whether the Company will be able to successfully implement its c omm ercialization plans for INVELTYS and EYSUVIS, if
approved; whether the market opportunity for INVELTYS and EYSUVIS is consistent with the Company’s expectations and market re search; whether any additional clinical trials
will be initiated or required for EYSUVIS prior to approval of the NDA, or at all, and whether the NDA for EYSUVIS will be ap proved on the timeline expected or at all; the
Company’s ability execute on the commercial launch of EYSUVIS, if and when approved, on the timeline expected, or at all; whe ther the Company will be able to generate its
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