Arcturus Therapeutics Announces Fourth Quarter and Full Year 2020 Financial Results and Positive Clinical Updates

Arcturus Therapeutics Announces Fourth Quarter and Full Year 2020 Financial Results and Positive Clinical Updates




Arcturus Therapeutics Announces Fourth Quarter and Full Year 2020 Financial Results and Positive Clinical Updates

ARCT-021 single-shot COVID-19 STARR™ mRNA vaccine to be advanced to Phase 3 clinical development – on track to initiate Phase 3 study in Q2

ARCT-021 single shot immunogenicity profile compares favorably with new data generated from recipients of a single dose of an approved conventional mRNA vaccine

ARCT-810 mRNA therapeutic for ornithine transcarbamylase deficiency to be advanced to Phase 2 clinical development – on track to file CTA for Phase 2 multiple dose study in Q2

ARCT-032 mRNA therapeutic for cystic fibrosis: completed successful pre-IND interaction with FDA – on track to file CTA in Q4

Investor conference call at 4:30 p.m. ET today

SAN DIEGO–(BUSINESS WIRE)–$ARCT #ClinicalTrial–Arcturus Therapeutics Holdings Inc. (the “Company”, “Arcturus”, Nasdaq: ARCT), a leading clinical-stage messenger RNA medicines company focused on the development of infectious disease vaccines and significant opportunities within liver and respiratory rare diseases, today announced its financial results for the quarter and full year ended December 31, 2020 and provided a corporate update.

“Based on highly promising clinical data from our Phase 1/2 study and emerging mRNA vaccine immunological data, we are advancing ARCT-021 for further development in Phase 3. We are presently preparing to move forward a 5 µg single dose regimen, to be confirmed based on pending Phase 2 data. Our self-amplifying mRNA-based investigational vaccine may provide a differentiated clinical profile and characteristics that support widespread distribution across the globe. Our expectation is that successful protection from COVID-19 will require repeated vaccination of billions of individuals for years to come and that ARCT-021 will be re-dosable. We believe that a re-dosable, more easily distributable single shot mRNA vaccine would be a valuable option for many countries,” said Joseph Payne, President and CEO of Arcturus.

“In addition to advancing our vaccine franchise, we have made continued progress advancing our pipeline of promising liver and lung mRNA therapeutic candidates. After successfully beginning enrollment in the U.S. for our Phase 1b study for ARCT-810, a therapeutic candidate for Ornithine Transcarbamylase (OTC) Deficiency, we have now also received approval from Health Canada to enroll subjects. We look forward to obtaining clinical data this year,” concluded Mr. Payne.

Recent Corporate Highlights

ARCT-021, Vaccine Candidate for SARS-CoV-2

1) Ongoing Phase 2 clinical study and planning for Phase 3 development:

  • More than 500 participants dosed across USA and Singapore
  • Phase 3 study initiation remains on track for Q2
  • Targeting application for Emergency Use Authorization in one or more jurisdictions in H2 2021

2) Encouraging new supportive data from Duke-NUS Medical School submitted for publication:

  • Dr. Eng Eong Ooi, Professor of Emerging Infectious Diseases at Duke-NUS Medical School, and colleagues, examined the adaptive immune responses of an approved conventional mRNA vaccine after a single administration
  • Data suggest that binding antibodies and cellular immunity are associated with COVID-19 protection at early timepoints after the first injection
  • ARCT-021 single shot immunogenicity profile in Phase 1/2 study compares favorably, providing additional support for the potential efficacy of the ARCT-021 vaccine

 

Day

BNT162b2

(30 µg); N=20

ARCT-021

(5µg); N=22

IgG (≥ 4-fold rises)

10

80%

14

81%*

PRNT (% Detectable)

10

10%

28

59%

ELISpot (SFUs)

Median change from baseline

10

28

15

211

21

13

*Increases to 100% by Day 36
IgG = Immunoglobulin G binding antibodies to full length spike protein
PRNT = plaque reduction neutralization test
SFUs = Spot Forming Units per million peripheral blood mononuclear cells

3) Completed Phase 1/2 clinical study and supporting preclinical studies:

  • Phase 1/2 study is complete and final data are under analysis; plan to submit results for publication in Q2
  • ARCT-021 demonstrated robust protection with single dose in a primate challenge model and in a human ACE2 receptor transgenic mouse challenge model
  • ARCT-021 demonstrated robust protection with a single dose in mice depleted of B cells, whereas depletion of T lymphocytes yielded no protection following virus challenge, emphasizing the importance of ARCT-021 induced cellular immunity

4) Manufacturing:

  • Recently received $46.6M from Singapore EDB to support ARCT-021 stockpiling
  • Manufacturing of lyophilized ARCT-021 to support Phase 3 and initial commercial supply well on track
  • Stability studies for lyophilized ARCT-021 at -20°C, 2-8°C and room temperature storage conditions ongoing

5) Agreements:

  • Strategic, government, and country supply agreement discussions continue to progress

ARCT-810, Therapeutic Candidate for Ornithine Transcarbamylase (OTC) Deficiency

  • Received approval from Health Canada to enroll subjects into Phase 1b study
  • CTA filing for Phase 2 multiple dose study on track for Q2

ARCT-032, Therapeutic Candidate for Cystic Fibrosis

  • Completed successful pre-IND interaction with FDA
  • CTA filing on track for Q4

Acquisition of Exclusive License to mRNA Manufacturing Technology from Alexion Pharmaceuticals

  • The technology supports Arcturus’ highly efficient processes to manufacture high purity mRNA vaccine and therapeutic candidates at kilogram scale
  • Extends the substantial intellectual property portfolio held by Arcturus

Financial results for the quarter and full year ended December 31, 2020

Revenues in conjunction with strategic alliances and collaborations: Arcturus’ primary source of revenues is from license fees and collaboration payments received from research and development arrangements with our pharmaceutical and biotechnology partners.

On a quarterly basis, total revenue for the three months ended December 31, 2020 was $2.2 million and was relatively flat when compared to the $2.3 million of the quarter ended September 30, 2020.

On a yearly basis, reported revenues of $9.5 million during the year ended December 31, 2020, decreased from $20.8 million in the year ended December 31, 2019. The decline in collaboration revenues primarily relates to three factors: a $5.6 million decrease in reimbursements from CureVac associated with the OTC collaboration that ended in the third quarter of 2019, a decrease in one-time license revenue of $3.3 million from Synthetic Genomics that occurred in 2019, and lower activity with other collaboration partners.

Operating expenses: On a quarterly basis, total operating expenses for the three months ended December 31, 2020 were $33.3 million compared with $23.3 million for quarter ended September 30, 2020, and $13.8 million in same period of 2019. Approximately $8 million of the sequential increase in operating expenses during the quarter ended December 31, 2020 was due to the ramp in the Covid-19 program related expenses, which included additional personnel, manufacturing and clinical trial expenses. The current quarter operating expenses were partially offset by $2.7 million in funds awarded under the Singapore vaccine grants and by the Cystic Fibrosis Foundation.

On a yearly basis, total operating expenses were $81.1 million for the year-ended December 31, 2020 compared with $46.3 million for the year ended December 31, 2019. The current year operating expenses were partially offset by $15.2 million of funds earned under the Singapore vaccine grants and funds awarded by the Cystic Fibrosis Foundation. The increase in net expenditures for the year ended December 31, 2020 as compared to the prior year was due primarily to the increased activity in clinical and manufacturing expenditures related to the Company’s Covid-19 and OTC programs as well as increased personnel costs and other facility costs related to the organizational growth of the Company.

Net loss: For the three months ended December 31, 2020 Arcturus reported a net loss of approximately $31.1 million, or ($1.25) per basic and diluted share, compared with a net loss in the three months ended September 30, 2020 of $21.0 million, or ($0.92) per basic and diluted share, and three months ended December 31, 2019 of $11.0 million, or ($0.76) per basic and diluted share.

For the year ended December 31, 2020, net loss was approximately $72.1 million, or ($3.55) per basic and diluted share, compared with a net loss for the year ended 2019 of $26.0 million, or ($2.15) per basic and diluted share.

Cash and Cash Equivalents: The Company’s cash balance was $463.0 million as of December 31, 2020, compared to cash and cash equivalents of $301.1 million on September 30, 2020. The increase in cash and cash equivalents compared to the prior year is primarily due to the receipt of approximately $162 million in net proceeds from our December 2020 public offering. Subsequent to the end of the quarter, in January 2021 the Company received $46.6 million in funds under a manufacturing loan from Singapore EDB for our Covid-19 vaccine program. Based on our current pipeline, the Company’s cash position is expected to be sufficient to support operations for more than two years.

Monday, March 1 @ 4:30 p.m. ET

Domestic:

877-407-0784

International:

201-689-8560

Conference ID:

13716298

Webcast:

http://public.viavid.com/index.php?id=143486

About Arcturus Therapeutics

Founded in 2013 and based in San Diego, California, Arcturus Therapeutics Holdings Inc. (Nasdaq: ARCT) is a clinical-stage mRNA medicines and vaccines company with enabling technologies: (i) LUNAR® lipid-mediated delivery, (ii) STARR™ mRNA Technology and (iii) mRNA drug substance along with drug product manufacturing expertise. Arcturus’ diverse pipeline of RNA therapeutic and vaccine candidates includes mRNA vaccine programs for SARS-CoV-2 (COVID-19) and Influenza, and other programs to potentially treat Ornithine Transcarbamylase (OTC) Deficiency, and Cystic Fibrosis along with partnered programs including Glycogen Storage Disease Type 3, Hepatitis B Virus, and non-alcoholic steatohepatitis (NASH). Arcturus’ versatile RNA therapeutics platforms can be applied toward multiple types of nucleic acid medicines including messenger RNA, small interfering RNA, replicon RNA, antisense RNA, microRNA, DNA, and gene editing therapeutics. Arcturus’ technologies are covered by its extensive patent portfolio (209 patents and patent applications, issued in the U.S., Europe, Japan, China and other countries). Arcturus’ commitment to the development of novel RNA therapeutics has led to collaborations with Janssen Pharmaceuticals, Inc., part of the Janssen Pharmaceutical Companies of Johnson & Johnson, Ultragenyx Pharmaceutical, Inc., Takeda Pharmaceutical Company Limited, CureVac AG, Synthetic Genomics Inc., Duke-NUS Medical School, and the Cystic Fibrosis Foundation. 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, collaborations, the likelihood of success, and the efficacy or safety, of the Company’s pipeline, including ARCT-021, ARCT-810 or ARCT-032, the planned initiation, design or completion of clinical trials, the likelihood that the Company will obtain clearance from regulatory authorities to proceed with planned clinical trials, the likelihood that preclinical or clinical data will be predictive of future clinical results, the likelihood that clinical data will be sufficient for regulatory approval or completed in time to submit an application for regulatory approval within a particular timeframe, the ability to enroll subjects in clinical trials, the Company’s efforts to develop a vaccine against COVID-19 and therapeutic potential thereof based on the Company’s mRNA therapeutics, the ability of the Company to scale up manufacturing of vaccine doses or to manufacture and scale up manufacturing of any other product or substance, the likelihood that a patent will issue from any patent application, the results of advancements in the Company’s manufacturing methods and technologies, including purification and lyophilization, its current cash position and expected cash burn and the impact of general business and economic conditions. Actual results and performance could differ materially from those projected in any forward-looking statements as a result of many factors including, without limitation, the ability to enroll subjects in clinical trials as a result of the COVID-19 pandemic, the impact of commercialization of third-party COVID-19 vaccines on the design, and ability to conduct, clinical trials, the availability of manufacturing capacity and raw materials, unexpected clinical results, and general market conditions that may prevent such achievements or performance. Arcturus may not actually achieve the plans, carry out the intentions or meet the expectations or projections disclosed in any forward-looking statements such as the foregoing and you should not place undue reliance on such forward-looking statements. Such statements are based on management’s current expectations and involve risks and uncertainties, including those discussed under the heading “Risk Factors” in Arcturus’ Annual Report on Form 10-K for the fiscal year ended December 31, 2020, and in subsequent filings with, or submissions to, the SEC. Except as otherwise required by law, Arcturus disclaims any intention or obligation to update or revise any forward-looking statements, which speak only as of the date they were made, whether as a result of new information, future events or circumstances or otherwise.

ARCTURUS THERAPEUTICS HOLDINGS INC. AND ITS SUBSIDIARIES

CONSOLIDATED BALANCE SHEETS

(in thousands, except par value information)

 

 

 

As of December 31,

 

 

 

2020

 

 

2019

 

Assets

 

 

 

 

 

 

 

 

Current assets:

 

 

 

 

 

 

 

 

Cash and cash equivalents

 

$

462,895

 

 

$

71,353

 

Accounts receivable

 

 

2,125

 

 

 

2,179

 

Prepaid expenses and other current assets

 

 

2,769

 

 

 

758

 

Total current assets

 

 

467,789

 

 

 

74,290

 

Property and equipment, net

 

 

3,378

 

 

 

2,349

 

Operating lease right-of-use asset, net

 

 

5,182

 

 

 

5,134

 

Equity-method investment

 

 

 

 

 

263

 

Non-current restricted cash

 

 

107

 

 

 

107

 

Total assets

 

$

476,456

 

 

$

82,143

 

Liabilities and stockholders’ equity

 

 

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

 

 

 

Accounts payable

 

$

10,774

 

 

$

5,793

 

Accrued liabilities

 

 

20,639

 

 

 

7,134

 

Deferred revenue

 

 

18,108

 

 

 

8,397

 

Total current liabilities

 

 

49,521

 

 

 

21,324

 

Deferred revenue, net of current portion

 

 

12,512

 

 

 

15,182

 

Long-term debt, net of current portion

 

 

13,845

 

 

 

14,995

 

Operating lease liability, net of current portion

 

 

4,025

 

 

 

4,850

 

Total liabilities

 

 

79,903

 

 

 

56,351

 

Stockholders’ equity:

 

 

 

 

 

 

 

 

Common stock: $0.001 par value; 60,000 shares authorized and 26,192 shares issued and outstanding at December 31, 2020; 30,000 shares authorized and 15,138 shares issued and outstanding at December 31, 2019

 

 

26

 

 

 

15

 

Additional paid-in capital

 

 

540,343

 

 

 

97,445

 

Accumulated deficit

 

 

(143,816

)

 

 

(71,668

)

Total stockholders’ equity

 

 

396,553

 

 

 

25,792

 

Total liabilities and stockholders’ equity

 

$

476,456

 

 

$

82,143

 

ARCTURUS THERAPEUTICS HOLDINGS INC. AND ITS SUBSIDIARIES

CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS

(in thousands, except per share data)

 

 

 

Year Ended December 31,

 

 

 

2020

 

 

2019

 

 

2018

 

Collaboration revenue

 

$

9,539

 

 

$

20,789

 

 

$

15,753

 

Operating expenses:

 

 

 

 

 

 

 

 

 

 

 

 

Research and development, net

 

 

57,846

 

 

 

33,640

 

 

 

16,982

 

General and administrative

 

 

23,217

 

 

 

12,662

 

 

 

20,582

 

Total operating expenses

 

 

81,063

 

 

 

46,302

 

 

 

37,564

 

Loss from operations

 

 

(71,524

)

 

 

(25,513

)

 

 

(21,811

)

Loss from equity-method investment

 

 

(263

)

 

 

(32

)

 

 

(302

)

Finance (expense) income, net

 

 

(361

)

 

 

(446

)

 

 

328

 

Net loss

 

 

(72,148

)

 

 

(25,991

)

 

 

(21,785

)

Net loss per share, basic and diluted

 

$

(3.55

)

 

$

(2.15

)

 

$

(2.16

)

Weighted-average shares outstanding, basic and diluted

 

 

20,305

 

 

 

12,069

 

 

 

10,069

 

Comprehensive loss:

 

 

 

 

 

 

 

 

 

 

 

 

Net loss

 

$

(72,148

)

 

$

(25,991

)

 

$

(21,785

)

Unrealized gain on short-term investments

 

 

 

 

 

 

 

 

3

 

Comprehensive loss

 

$

(72,148

)

 

$

(25,991

)

 

$

(21,782

)

 

 

Fourth Quarter 2019

(unaudited)

 

 

First Quarter 2020

(unaudited)

 

 

Second Quarter 2020

(unaudited)

 

 

Third Quarter 2020

(unaudited)

 

 

Fourth Quarter 2020

(unaudited)

 

Collaboration revenue

 

$

2,968

 

 

$

2,646

 

 

$

2,322

 

 

$

2,333

 

 

$

2,238

 

Research and development expenses, net

 

 

11,994

 

 

 

7,917

 

 

 

7,944

 

 

 

17,699

 

 

 

24,286

 

General and administrative expenses

 

 

1,791

 

 

 

4,191

 

 

 

4,420

 

 

 

5,572

 

 

 

9,034

 

Loss from operations

 

 

(10,817

)

 

 

(9,462

)

 

 

(10,042

)

 

 

(20,938

)

 

 

(31,082

)

Net loss

 

 

(10,989

)

 

 

(9,777

)

 

 

(10,263

)

 

 

(21,004

)

 

 

(31,104

)

Net loss per share, basic and diluted

 

$

(0.76

)

 

$

(0.67

)

 

$

(0.55

)

 

$

(0.92

)

 

$

(1.25

)

Weighted average shares outstanding, basic and diluted

 

 

14,505

 

 

 

14,521

 

 

 

18,794

 

 

 

22,938

 

 

 

24,886

 

 

Contacts

IR and Media Contacts
Arcturus Therapeutics

Neda Safarzadeh

(858) 900-2682

IR@ArcturusRx.com

Kendall Investor Relations

Carlo Tanzi, Ph.D.

(617) 914-0008

ctanzi@kendallir.com