U.S. Securities and Exchange Commission
September 18, 2020
Page Two
2. | On page 5, please revise the table to disclose all remaining stages you must successfully complete before you could seek FDA approval. For example, please revise to reference Phase 3 trials and any estimated timetable. In this regard, we note your disclosure on pages 132 - 133 regarding Phase 1, Phase 2, and Phase 3 clinical trials. |
Response: In response to the Staff’s comment, the Company has revised the disclosure on pages 5, 15, and 112 of the Registration Statement to reference the possibility that the Company may be required by the U.S. Food and Drug Administration (“FDA”) and comparable foreign regulatory authorities to initiate one or more additional clinical trials, including a Phase 3 clinical trial or trials. However, the Company advises the Staff that the estimated timing or scope of any such future clinical trials is not currently ascertainable, as the design, duration, and scope of such clinical trials will be decided upon after further discussions with the FDA or comparable foreign regulatory authorities. The Company has expanded the disclosure on page 15 of the Registration Statement to more clearly address this uncertainty.
Risk Factors
Our amended and restated certificate of incorporation and amended and restated bylaws will provide that..., page 76
3. | Please revise your disclosure on pages 76 and 185 regarding choice of forum for consistency. In particular, please revise the first sentence under “Choice of Forum” on page 185 to clarify that both your amended and restated bylaws and amended and restated certificate of incorporation include such provision, and similarly, revise the second paragraph of the risk factor to clarify that both documents provide that the federal district courts of the United States of America will be the exclusive forum for resolving any complaint asserting a cause of action arising under the Securities Act. |
Response: In response to the Staff’s comment, the Company has revised the disclosure on pages 77, 78, and 188 of the Registration Statement.
Management’s Discussion and Analysis of Financial Condition and Results of Operations
License Agreement with Eli Lilly and Company, page 92
4. | You disclose on pages 92 and F-44 that in May 2016, you entered into a License Agreement with Lilly, which could require you to pay Lilly up to an aggregate of $23.0 million upon the achievement of certain clinical and commercialization milestones. Please revise to describe such milestones in greater detail, including how they will be calculated and any timeframe, as applicable. |
Response: In response to the Staff’s comment, the Company has revised the disclosure on pages 94, 129, F-21, and F-45 of the Registration Statement.
Loan Agreement, page 97
5. | Please expand to provide more detailed disclosure of any material financial covenants contained in your Loan Agreement, including quantifying any ratios, as applicable. If any of such covenants could materially impact your ability to obtain additional debt financing, please revise your “Funding Requirements” disclosure on page 98 to disclose the same, and expand your risk factor disclosure as appropriate. |
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