Arcturus Therapeutics Announces First Quarter 2023 Financial Update and Pipeline Progress
New Drug Application (NDA) for ARCT-154, a next generation COVID-19 vaccine, was submitted in
ARCT-032 Phase 1 enrollment and administration completed successfully; trial expansion to include Cystic Fibrosis patients planned in third quarter
Investor conference call at
“We are very pleased to announce the first NDA submission for the COVID-19 vaccine, ARCT-154, in
In
“As we mentioned on the year end conference call last month, we took a number of positive steps to improve our balance sheet this quarter with the elimination of
Recent Corporate Highlights
- A New Drug Application (NDA) for ARCT-154 was submitted in April by
Meiji Seika Pharma to theJapanese Pharmaceuticals andMedical Devices Agency (PMDA). This filing included a Phase 3 efficacy and safety study (N > 16,000), conducted inVietnam that met its primary endpoint of prevention of COVID-19 disease during a period when there were multiple variants of concern. - The ARCT-154 Phase 3 study being conducted by
Meiji Seika Pharma has completed enrollment (N = 828). This non-inferiority study is designed to evaluate the safety and immunogenicity of ARCT-154 compared to Comirnaty® (Pfizer/BioNTech), administered as a booster dose. The interim analysis data will be submitted to the PMDA to seek registration of the ARCT-154 booster. - In April,
Meiji Seika Pharma entered into an agreement with CSL Seqirus wherebyMeiji Seika Pharma will be responsible for the distribution and sales of ARCT-154 inJapan . - ARCT-810, the Company’s mRNA therapeutic candidate for ornithine transcarbamylase deficiency (OTC), is being evaluated in a Phase 2 multiple dose study, designed to enroll up to 24 adolescents and adults with OTC deficiency. The Phase 2 study is being conducted in the
UK andEurope . The Company remains on track to share interim Phase 2 data on a subset of participants later in 2023. - ARCT-032, the Company’s inhaled mRNA therapeutic for cystic fibrosis (CF), has achieved the recruitment target and completed administration in a Phase 1 single ascending dosing study with 32 healthy participants (8 subjects per cohort). The safety and tolerability data support the study expansion and inclusion of patients with CF. Arcturus is amending the protocol to allow the dosing of patients with CF and expects to initiate the enrollment in Q3 2023.
Financial Results for the First Quarter Ended
Revenues in conjunction with strategic alliances and collaborations:
Arcturus’ primary sources of revenues were from license fees, consulting and related technology transfer fees, reservation fees and collaborative payments received from research and development arrangements with pharmaceutical and biotechnology partners. Total revenue for the three months ended
Operating expenses:
Total operating expenses for the three months ended
Research and development expenses:
Research and development expense was
General and Administrative Expenses:
General and administrative expenses were
Net Income and other income and expense:
For the three months ended
Cash Position and Balance Sheet:
Cash, cash equivalents and restricted cash were
- Domestic: 1-888-886-7786
- International: 1-416-764-8658
- Conference ID: 70942720
- Webcast: Link
About Arcturus Therapeutics
Founded in 2013 and based in San Diego, California, Arcturus Therapeutics Holdings Inc. (Nasdaq: ARCT) is a global late-stage clinical mRNA medicines and vaccines company with enabling technologies: (i) LUNAR® lipid-mediated delivery, (ii) STARR™ mRNA Technology (samRNA) and (iii) mRNA drug substance along with drug product manufacturing expertise. Arcturus’ pipeline includes RNA therapeutic candidates to potentially treat ornithine transcarbamylase (OTC) deficiency and cystic fibrosis, along with its partnered mRNA vaccine programs for SARS-CoV-2 (COVID-19) and influenza. Arcturus’ versatile RNA therapeutics platforms can be applied toward multiple types of nucleic acid medicines including messenger RNA, small interfering RNA, circular RNA, antisense RNA, self-amplifying RNA, DNA, and gene editing therapeutics. Arcturus’ technologies are covered by its extensive patent portfolio (patents and patent applications issued in the U.S., Europe, Japan, China, and other countries). For more information, visit www.ArcturusRx.com. In addition, please connect with us on Twitter and LinkedIn.
Forward Looking Statements
This press release contains forward-looking statements that involve substantial risks and uncertainties for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. Any statements, other than statements of historical fact included in this press release, are forward-looking statements, including those regarding strategy, future operations, the likelihood of success of the Company’s pipeline (including ARCT-032 and ARCT-810) and partnered programs (including the COVID-19 and flu programs partnered with CSL Seqirus), the potential of ARCT-154 to offer effective or long-lasting protection against COVID-19 disease, the potential for the Company’s platform to result in novel vaccines or therapeutics, the anticipated timing and sharing of Phase 3 pivotal ARCT-154 results and data, the planned production of ARCT-154 doses, the likelihood and timing of regulatory approvals or orders for, or commercialization of, ARCT-154 in
Trademark Acknowledgements
The Arcturus logo and other trademarks of Arcturus appearing in this announcement, including LUNAR® and STARR™, are the property of Arcturus. All other trademarks, services marks, and trade names in this announcement are the property of their respective owners.
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CONDENSED CONSOLIDATED BALANCE SHEETS |
||||||||
|
|
|
|
|
||||
(in thousands, except par value information) |
|
(unaudited) |
|
|
||||
Assets |
|
|
|
|
||||
Current assets: |
|
|
|
|
||||
Cash and cash equivalents |
|
$ |
327,935 |
|
|
$ |
391,883 |
|
Accounts receivable |
|
|
92,483 |
|
|
|
2,764 |
|
Prepaid expenses and other current assets |
|
|
4,137 |
|
|
|
8,686 |
|
Total current assets |
|
|
424,555 |
|
|
|
403,333 |
|
Property and equipment, net |
|
|
12,635 |
|
|
|
12,415 |
|
Operating lease right-of-use asset, net |
|
|
31,557 |
|
|
|
32,545 |
|
Non-current restricted cash |
|
|
2,116 |
|
|
|
2,094 |
|
Total assets |
|
$ |
470,863 |
|
|
$ |
450,387 |
|
Liabilities and stockholders’ equity |
|
|
|
|
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Current liabilities: |
|
|
|
|
||||
Accounts payable |
|
$ |
19,344 |
|
|
$ |
7,449 |
|
Accrued liabilities |
|
|
32,293 |
|
|
|
30,232 |
|
Current portion of long-term debt |
|
|
— |
|
|
|
60,655 |
|
Deferred revenue |
|
|
38,493 |
|
|
|
28,648 |
|
Total current liabilities |
|
|
90,130 |
|
|
|
126,984 |
|
Deferred revenue, net of current portion |
|
|
20,569 |
|
|
|
20,071 |
|
Operating lease liability, net of current portion |
|
|
29,187 |
|
|
|
30,216 |
|
Other non-current liabilities |
|
|
1,729 |
|
|
|
2,804 |
|
Total liabilities |
|
$ |
141,615 |
|
|
$ |
180,075 |
|
Stockholders’ equity |
|
|
|
|
||||
Common stock, |
|
|
27 |
|
|
|
27 |
|
Additional paid-in capital |
|
|
616,608 |
|
|
|
608,426 |
|
Accumulated deficit |
|
|
(287,387 |
) |
|
|
(338,141 |
) |
Total stockholders’ equity |
|
|
329,248 |
|
|
|
270,312 |
|
Total liabilities and stockholders’ equity |
|
$ |
470,863 |
|
|
$ |
450,387 |
|
|
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CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE INCOME (LOSS) |
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(unaudited) |
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|
Three Months Ended |
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(in thousands, except per share data) |
|
2023 |
|
2022 |
|
2022 |
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Revenue: |
|
|
|
|
|
|
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Collaboration revenue |
|
$ |
79,729 |
|
|
$ |
5,244 |
|
|
$ |
160,049 |
|
Grant revenue |
|
|
556 |
|
|
|
— |
|
|
|
244 |
|
Total revenue |
|
|
80,285 |
|
|
|
5,244 |
|
|
|
160,293 |
|
Operating expenses: |
|
|
|
|
|
|
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Research and development, net* |
|
|
51,768 |
|
|
|
44,893 |
|
|
|
26,981 |
|
General and administrative* |
|
|
13,762 |
|
|
|
10,730 |
|
|
|
11,860 |
|
Total operating expenses |
|
|
65,530 |
|
|
|
55,623 |
|
|
|
38,841 |
|
Income (loss) from operations |
|
|
14,755 |
|
|
|
(50,379 |
) |
|
|
121,452 |
|
Loss from equity-method investment |
|
|
— |
|
|
|
(384 |
) |
|
|
— |
|
(Loss) gain from foreign currency |
|
|
(328 |
) |
|
|
158 |
|
|
|
(3,835 |
) |
Gain on debt extinguishment |
|
|
33,953 |
|
|
|
— |
|
|
|
— |
|
Finance income (expense), net |
|
|
2,477 |
|
|
|
(564 |
) |
|
|
1,025 |
|
Net income (loss) before income taxes |
|
|
50,857 |
|
|
|
(51,169 |
) |
|
|
118,642 |
|
Provision (benefit) for income taxes |
|
|
103 |
|
|
|
— |
|
|
|
1,295 |
|
Net income (loss) |
|
|
50,754 |
|
|
|
(51,169 |
) |
|
|
117,347 |
|
Earnings (loss) per share: |
|
|
|
|
|
|
||||||
Basic |
|
$ |
1.91 |
|
|
$ |
(1.94 |
) |
|
$ |
4.43 |
|
Diluted |
|
$ |
1.87 |
|
|
$ |
(1.94 |
) |
|
$ |
4.33 |
|
Weighted-average shares used in calculation of earnings (loss) per share: |
|
|
|
|
|
|
||||||
Basic |
|
|
26,555 |
|
|
|
26,376 |
|
|
|
26,508 |
|
Diluted |
|
|
27,149 |
|
|
|
26,376 |
|
|
|
27,080 |
|
Comprehensive income (loss): |
|
|
|
|
|
|
||||||
Net income (loss) |
|
|
50,754 |
|
|
|
(51,169 |
) |
|
|
117,347 |
|
Comprehensive income (loss) |
|
$ |
50,754 |
|
|
$ |
(51,169 |
) |
|
$ |
117,347 |
|
*Includes share-based compensation expense as follows: |
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|
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Three Months Ended |
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|
|
|
|
|
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(in thousands) |
|
2023 |
|
2022 |
|
2022 |
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Research and development |
|
$ |
3,508 |
|
|
$ |
3,455 |
|
|
$ |
3,270 |
|
General and administrative |
|
|
4,674 |
|
|
|
3,916 |
|
|
|
3,260 |
|
View source version on businesswire.com: https://www.businesswire.com/news/home/20230509006157/en/
IR and Media Contacts
VP, Head of IR/PR/Marketing
(858) 900-2682
IR@ArcturusRx.com
Kendall Investor Relations
(617) 914-0008
ctanzi@kendallir.com
Source: