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Delaware |
81‑5395687 |
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(State of Other Jurisdiction of incorporation or Organization) |
(I.R.S. Employer Identification No.) |
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350 Fifth Avenue, 72nd Floor, Suite 7240 |
10118 |
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(Address of principal executive offices) |
(Zip code) |
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Name Of Each Exchange |
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Title of Each Class |
Trading Symbol(s) |
On Which Registered |
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Common Stock, $0.0001 Par Value per Share |
HOOK |
The Nasdaq Global Select Market |
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Large accelerated filer ☐ |
Accelerated filer ☐ |
Non-accelerated filer ☒ |
Smaller reporting company ☒ |
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Emerging growth company ☒ |
2
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the success, cost and timing of our product development activities and clinical trials; |
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the timing, scope or likelihood of regulatory filings and approvals, including timing of Investigational New Drug Application and Biological Licensing Application filings for our current and future product candidates, and final U.S. Food and Drug Administration, European Medicines Agency or other foreign regulatory authority approval of our current and future product candidates; |
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our ability to develop and advance our current product candidates and programs into, and successfully complete, clinical studies; |
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our manufacturing, commercialization and marketing capabilities and strategy; |
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the potential benefits of and our ability to maintain our collaboration with Gilead Sciences, Inc., and establish or maintain future collaborations or strategic relationships or obtain additional funding; |
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the rate and degree of market acceptance and clinical utility of our current and future product candidates; |
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our intellectual property position, including the scope of protection we are able to establish and maintain for intellectual property rights covering our VaxWave and TheraT technologies and the product candidates based on these technologies, the validity of intellectual property rights held by third parties, and our ability not to infringe, misappropriate or otherwise violate any third-party intellectual property rights; |
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future agreements with third parties in connection with the commercialization of our product candidates and any other approved product; |
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regulatory developments in the United States and foreign countries; |
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competitive companies, technologies and our industry and the success of competing therapies that are or may become available; |
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our ability to attract and retain key scientific or management personnel; |
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our ability to obtain funding for our operations, including funding necessary to complete further development and commercialization of our product candidates; |
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the accuracy of our estimates of our annual total addressable market, future revenue, expenses, capital requirements and needs for additional financing; |