Exicure, Inc. Reports Full Year 2021 Financial Results and Corporate Progress
Exicure, Inc. (NASDAQ: XCUR) reported a significant net loss of $64.1 million for 2021, up from $24.7 million in 2020, driven by decreased non-cash revenue and higher R&D expenses totaling $49.0 million. Revenue decreased to $(0.5) million from $16.6 million in 2020, largely due to changes in the AbbVie collaboration. As of December 31, 2021, cash reserves amounted to $48.3 million. The company anticipates reporting results from initial SCN9A in vivo studies by year-end 2022 and is focused on strategic partnerships and out-licensing opportunities in 2022.
- Anticipation of initial in vivo study results for SCN9A by year-end 2022.
- Focus on strategic partnerships, including a collaboration with Ipsen targeting neurodegenerative disorders.
- Net loss increased to $64.1 million in 2021, raising concerns about operational sustainability.
- Revenue declined significantly, reflecting a $17.1 million decrease from the previous year.
- Continues to advance preclinical discovery of its SCN9A research program, anticipates reporting results from initial in vivo animal studies by year-end 2022
- Continues progression of work with partnered programs, with plan of meeting potential pre-clinical milestones in 2023
“This past year brought significant challenges to our organization that prompted strategic decisions at year-end to refocus our business strategy on our next generation pipeline and investments in neuroscience in order to be cash efficient,” said
Corporate Progress
Corporate highlights for 2021 include:
-
Entered into an exclusive collaboration targeting rare neurodegenerative disorders with Ipsen in
July 2021 to research, develop, and commercialize novel Spherical Nucleic Acids (SNAs) as potential investigational treatments for Huntington’s disease (HD) and Angelman syndrome (AS).
- Completed a strategic review in fourth quarter of 2021, which resulted in a restructuring and pipeline focus on preclinical programs targeting SCN9A in pain and partnered programs.
-
Completed a
registered direct offering in$11.5 million December 2021 .
Priorities for 2022 include:
-
Advancement of the Company’s SCN9A preclinical discovery program.
Exicure anticipates results from initial in vivo animal studies by year-end 2022 with goal of therapeutic candidate selection in the second half of 2023.
- Progressing work with the Company’s partnered programs, with plan of meeting potential pre-clinical milestones in 2023.
- Actively pursuing strategic out-license opportunities for cavrotolimod.
- Ongoing pursuit of near-term partnering opportunities for pain and other neuroscience programs.
2021 Financial Results
Cash Position: Cash, cash equivalents and short-term investments were
Revenue: Revenue was
Research and Development (R&D) Expense: Research and development expenses were
General and Administrative (G&A) Expense: General and administrative expenses were
Net Loss: The Company had a net loss of
Going Concern: The Company’s expectation to continue to generate operating losses and negative operating cash flows in the future and the need for additional funding to support its planned operations raise substantial doubt regarding its ability to continue as a going concern within one year after the date that its consolidated financial statements for the year ended
About
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements in this press release other than statements of historical fact may be deemed forward looking including, but not limited to: statements regarding the Company’s business plans and objectives; the substantial doubt about the Company’s ability to continue as a going concern; the Company’s anticipated cash runway; the Company’s ability to grow its strategic partnerships and the potential achievement of any clinical trial milestones pursuant to license and collaboration agreements; the continuation of pre-clinical discovery of potential therapeutic candidates and the ability to develop, and possibly partner, product candidates for the treatment of neurological conditions; the potential advantages and clinical benefit of the Company’s SNA platform and advancement of SCN9A preclinical discovery and the timing of results from initial studies and therapeutic candidate selection; the pursuit of out-license opportunities for cavrotolimod; the future prospects of the Company; and the Company’s ability to execute on programs and reduce overall costs. Words such as “plans,” “expects,” “will,” “anticipates,” “continue,” “expand,” “advance,” “develop” “believes,” “guidance,” “target,” “may,” “remain,” “project,” “outlook,” “intend,” “estimate,” “could,” “should,” and other words and terms of similar meaning and expression are intended to identify forward-looking statements, although not all forward-looking statements contain such terms. Forward-looking statements are based on management’s current beliefs and assumptions that are subject to risks and uncertainties and are not guarantees of future performance. Actual results could differ materially from those contained in any forward-looking statement as a result of various factors, including, without limitation: market and other conditions; the Company’s ability to adequately finance its business and seek alternative sources of financing the risks that the ongoing COVID-19 pandemic may disrupt the Company’s business and/or the global healthcare system (including its supply chain) more severely than it has to date or more severely than anticipated; unexpected costs, charges or expenses that reduce the Company’s capital resources; the unproven approach of the Company’s SNA platform; the Company’s preclinical programs do not advance into clinical or result in approved products on a timely or cost effective basis or at all; the results of early clinical trials are not always being predictive of future results; the cost, timing and results of clinical trials; that many drug candidates do not become approved drugs on a timely or cost effective basis or at all; the ability to enroll patients in clinical trials; possible safety and efficacy concerns; regulatory developments; the ability of the Company to obtain or maintain its existing or future collaborations, licenses or contractual relationships and/or collaborate successfully with strategic partners; regulatory developments; exposure to litigation, including patent litigation, and/or regulatory actions; the ability of the Company to protect its intellectual property rights; and the impact of the completion of the Company’s previously reported internal investigation on the Company’s business and diversion of management time and attention on related issues, including any related investigations or proceedings, shareholder lawsuits, reputational harm, or the possibility that executives or other employees may resign. Given these risks and uncertainties, you are cautioned not to place undue reliance on such forward-looking statements. For a discussion of other risks and uncertainties, and other important factors, any of which could cause the Company’s actual results to differ from those contained in the forward-looking statements, see the section titled “Risk Factors” in the Company’s Quarterly Report on Form 10-Q for the quarter ended
UNAUDITED CONDENSED CONSOLIDATED BALANCE SHEETS (in thousands, except share and per share data) |
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2021 |
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2020 |
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ASSETS |
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Current assets: |
|
|
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Cash and cash equivalents |
$ |
34,644 |
|
|
$ |
33,262 |
|
Short-term investments |
|
4,497 |
|
|
|
48,818 |
|
Accounts receivable |
|
— |
|
|
|
11 |
|
Prepaid expenses and other assets |
|
4,525 |
|
|
|
4,231 |
|
Total current assets |
|
43,666 |
|
|
|
86,322 |
|
Property and equipment, net |
|
3,927 |
|
|
|
4,123 |
|
Right-of-use asset |
|
7,950 |
|
|
|
8,606 |
|
Other noncurrent assets |
|
9,325 |
|
|
|
1,393 |
|
Total assets |
$ |
64,868 |
|
|
$ |
100,444 |
|
LIABILITIES AND STOCKHOLDERS’ EQUITY |
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Current liabilities: |
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Current portion of long-term debt |
$ |
6,873 |
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|
$ |
— |
|
Accounts payable |
|
3,413 |
|
|
|
1,866 |
|
Accrued expenses and other current liabilities |
|
6,464 |
|
|
|
3,525 |
|
Deferred revenue, current |
|
17,317 |
|
|
|
8,343 |
|
Total current liabilities |
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34,067 |
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|
|
13,734 |
|
Long-term debt, net |
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— |
|
|
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16,589 |
|
Deferred revenue, noncurrent |
|
11,509 |
|
|
|
— |
|
Lease liability, noncurrent |
|
7,404 |
|
|
|
7,959 |
|
Other noncurrent liabilities |
|
656 |
|
|
|
656 |
|
Total liabilities |
$ |
53,636 |
|
|
$ |
38,938 |
|
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Stockholders’ equity: |
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Preferred stock, |
|
— |
|
|
|
— |
|
Common stock, |
|
11 |
|
|
|
9 |
|
Additional paid-in capital |
|
181,290 |
|
|
|
167,379 |
|
Accumulated other comprehensive (loss) income |
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(2 |
) |
|
|
83 |
|
Accumulated deficit |
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(170,067 |
) |
|
|
(105,965 |
) |
Total stockholders' equity |
|
11,232 |
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|
|
61,506 |
|
Total liabilities and stockholders’ equity |
$ |
64,868 |
|
|
$ |
100,444 |
|
UNAUDITED CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (in thousands, except share and per share data) |
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Year Ended
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2021 |
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2020 |
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Revenue: |
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Collaboration revenue |
$ |
(483 |
) |
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$ |
16,613 |
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Total revenue |
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(483 |
) |
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16,613 |
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Operating expenses: |
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Research and development expense |
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48,979 |
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32,094 |
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General and administrative expense |
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13,087 |
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|
|
9,955 |
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Total operating expenses |
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62,066 |
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42,049 |
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Operating loss |
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(62,549 |
) |
|
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(25,436 |
) |
Other (expense) income, net: |
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Dividend income |
|
8 |
|
|
|
47 |
|
Interest income |
|
141 |
|
|
|
972 |
|
Interest expense |
|
(1,691 |
) |
|
|
(573 |
) |
Other (expense) income, net |
|
(11 |
) |
|
|
322 |
|
Total other (expense) income, net |
|
(1,553 |
) |
|
|
768 |
|
Net loss before provision for income taxes |
|
(64,102 |
) |
|
|
(24,668 |
) |
Provision for income taxes |
|
— |
|
|
|
— |
|
Net loss |
$ |
(64,102 |
) |
|
$ |
(24,668 |
) |
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Basic and diluted loss per common share |
$ |
(0.72 |
) |
|
$ |
(0.28 |
) |
Weighted-average basic and diluted common shares outstanding |
|
88,617,332 |
|
|
|
87,203,588 |
|
View source version on businesswire.com: https://www.businesswire.com/news/home/20220325005435/en/
Media:
MacDougall
781-235-3060
ksharma@macbiocom.com
Source:
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