$ARCT earnings report

Arcturus Therapeutics Announces Third Quarter 2026 Financial Results and Pipeline Progress. AlphAI read Arcturus Therapeutics Holdings's Third quarter 2026 filing as mixed. 2 quarters are on record below.

Third quarter 2026

AlphAI · Earnings readARCT · Third quarter 2026 · ended September 30, 2026

Arcturus Therapeutics Announces Third Quarter 2026 Financial Results and Pipeline Progress

→Mixed quarter

Third-quarter revenue increased and net loss narrowed versus the comparable period last year, supported by the CSL Seqirus termination payment and deferred-revenue recognition. Nine-month revenue declined and nine-month net loss widened, while the company continued to fund its rare-disease pipeline from a cash balance of $184.8 million and stated cash runway through year end 2028.

Revenue
$18.3M
EPS · GAAP
$(0.26)

Key metrics

shortened, hover for the filing’s print
MetricValueq/qy/y
Collaboration revenue, three months ended September 30, 2026GAAP$16.85M––
Grant revenue, three months ended September 30, 2026GAAP$1.45M––
Total revenue, three months ended September 30, 2026GAAP$18.3M––
Research and development expenses, three months ended September 30, 2026GAAP$17M––
General and administrative expenses, three months ended September 30, 2026GAAP$10.5M––
Total operating expenses, three months ended September 30, 2026GAAP$27.48M––
Loss from operations, three months ended September 30, 2026GAAP−$9.19M––
Finance income, net, three months ended September 30, 2026GAAP$1.77M––
Other expense, three months ended September 30, 2026GAAP−$2K––
Net loss before income taxes, three months ended September 30, 2026GAAP−$7.41M––
Net loss, three months ended September 30, 2026GAAP$7.4M––
Net loss per share, basic and diluted, three months ended September 30, 2026GAAP$(0.26)––
Weighted-average shares outstanding, basic and diluted, three months ended September 30, 2026GAAP28.44M––
Comprehensive loss, three months ended September 30, 2026GAAP−$7.41M––
Collaboration revenue, nine months ended September 30, 2026GAAP$18.34M––
Grant revenue, nine months ended September 30, 2026GAAP$4.97M––
Total revenue, nine months ended September 30, 2026GAAP$23.3M––
Research and development expenses, nine months ended September 30, 2026GAAP$56M––
General and administrative expenses, nine months ended September 30, 2026GAAP$30.9M––
Total operating expenses, nine months ended September 30, 2026GAAP$86.98M––
Loss from operations, nine months ended September 30, 2026GAAP−$63.66M––
Finance income, net, nine months ended September 30, 2026GAAP$5.52M––
Other expense, nine months ended September 30, 2026GAAP−$26K––
Provision for income taxes, nine months ended September 30, 2026GAAP—––
Net loss, nine months ended September 30, 2026GAAP$58.2M––
Net loss per share, basic and diluted, nine months ended September 30, 2026GAAP$(2.05)––
Weighted-average shares outstanding, basic and diluted, nine months ended September 30, 2026GAAP28.43M––
Comprehensive loss, nine months ended September 30, 2026GAAP−$58.16M––
Cash and cash equivalents, September 30, 2026GAAP$184.8M––
Total assets, September 30, 2026GAAP$215.3M––
Total liabilities, September 30, 2026GAAP$46.59M––
Total stockholders' equity, September 30, 2026GAAP$168.7M––

Amounts quoted below without a unit are in thousands, as in the filing’s tables. Per-share figures are as printed.

Pipeline milestones and cash runway outlook

  • NoteARCT-032 (CF) Phase 2 enrollment is expected to be completed by year-end.
  • NoteARCT-032 (CF) Phase 2 full data from Cohort 4 are planned for presentation in Q2 2027.
  • NoteArcturus plans to initiate ARCT-2601 Phase 2 dosing in Q1 2027, with top-line data expected in H2 2027.
  • NoteArcturus plans to submit an IND to the FDA for PKU in the second half of 2027.
  • Notecash runway of over two years through year end 2028
  • NoteKOSTAIVE® commercial activities in 2027.

What drove it

  • Third-quarter revenue recognition included the $12.0 million termination payment and remaining deferred revenue upon termination of the CSL Seqirus collaboration.
  • Reduced clinical and manufacturing activities, particularly across the LUNAR-COVID and BARDA programs, together with lower personnel and facilities costs, reduced research and development expenses.
  • Nine-month revenue was affected by lower revenue recognized under the CSL Seqirus collaboration prior to its termination and lower BARDA grant revenue.
  • ARCT-810 Phase 2 interim data at 0.3 mg/kg and 0.5 mg/kg showed meaningful biomarker activity and was generally safe and well tolerated.
  • LUNAR 2.0™ demonstrated 38-fold greater potency than the key lipid in ARCT-810 in a non-human primate study based on human ornithine transcarbamylase expression.

Concerns

  • Nine-month total revenue was $23.3 million, compared with $74.8 million in the comparable period last year.
  • Nine-month net loss was $58.2 million, compared with a net loss of $36.7 million for the nine months ended September 30, 2025.
  • Third-quarter revenue growth was primarily driven by a $12.0 million termination payment and remaining deferred revenue upon termination of the CSL Seqirus collaboration.
  • Cash and cash equivalents declined by $46.1 million from December 31, 2025 to September 30, 2026.
  • ARCT-032, ARCT-2601 and PKU milestones remain forward-looking plans subject to the risks described by the company.

What to watch

  • Completion of ARCT-032 Phase 2 enrollment by year-end and presentation of Cohort 4 full data in Q2 2027.
  • Timing of the ARCT-032 decision to proceed into Phase 3 and the associated significant contributions from Thermo Fisher Scientific.
  • Initiation of ARCT-2601 Phase 2 dosing in Q1 2027 and anticipated top-line data in H2 2027.
  • Submission of an IND to the FDA for PKU in the second half of 2027.
  • KOSTAIVE® commercial sales in Japan for the 2026/2027 season and preparation for commercial activities in the EU and UK in 2027.

Balance sheet and cash flow

  • Cash and cash equivalents were $184.8 million as of September 30, 2026, and $230.9 million on December 31, 2025, for a decrease of $46.1 million.
  • The decrease was primarily driven by cash used related to ongoing clinical development activities, including the continued advancement of the Company's cystic fibrosis and OTC deficiency programs, partially offset by the $12.0 million payment received from CSL Seqirus under the termination and settlement agreement.
  • Non-current restricted cash was $2,028 (in thousands) at September 30, 2026.
  • Operating lease liabilities, net of current portion, were $18,244 (in thousands) at September 30, 2026.

Analysis

Arcturus reported third-quarter total revenue of $18.3 million, compared with $17.2 million in the comparable period last year, while net loss narrowed to $7.4 million from $13.4 million. The revenue increase was primarily driven by recognition of the $12.0 million CSL Seqirus termination payment and remaining deferred revenue following termination of that collaboration, partially offset by lower grant revenue. Collaboration revenue was $16,852 (in thousands) and grant revenue was $1,445 (in thousands).

Cost discipline was evident in research and development expense of $17.0 million, compared with $23.3 million in the comparable quarter last year. The company attributed the reduction to lower clinical and manufacturing activity, particularly across LUNAR-COVID and BARDA programs, as well as lower personnel and facilities costs. General and administrative expense was comparatively stable at $10.5 million versus $10.4 million. Total operating expenses were $27,482 (in thousands), and loss from operations was $(9,185) (in thousands).

The nine-month figures show the dependence of the third-quarter revenue result on the CSL Seqirus termination-related recognition. Nine-month total revenue was $23.3 million versus $74.8 million in the comparable period last year, reflecting lower CSL Seqirus collaboration revenue before termination and lower BARDA grant revenue. Nine-month net loss was $58.2 million versus $36.7 million, even as nine-month research and development expense declined to $56.0 million from $87.7 million.

Cash and cash equivalents were $184.8 million at September 30, 2026, versus $230.9 million on December 31, 2025. The company cited ongoing clinical development spending, partly offset by the $12.0 million CSL Seqirus payment, and stated cash runway of over two years through year end 2028. Pipeline attention centers on expected ARCT-032 enrollment completion by year-end and Phase 2 data in Q2 2027, ARCT-2601 Phase 2 dosing planned for Q1 2027 with top-line data expected in H2 2027, and a planned PKU IND submission in the second half of 2027.

Management, verbatim

The third quarter marked a pivotal step forward for our liver therapeutics franchise, with encouraging ARCT-810 Phase 2 results and the introduction of LUNAR 2.0™, our next-generation mRNA delivery platform, which demonstrated a 38-fold improvement over the key lipid in ARCT-810 in non-human primates.

Joseph Payne, President & CEO of Arcturus

We continue to maintain a strong balance sheet and cash runway of over two years through year end 2028, allowing our company to reach important clinical and regulatory milestones for its rare disease pipeline.

Dennis Mulroy, Chief Financial Officer of Arcturus

Not in the filing

stated, not guessed
  • Non-GAAP financial metrics were not reported.
  • Gross profit and gross margin were not reported.
  • Operating cash flow was not reported.
  • Free cash flow was not reported.
  • Debt was not reported.
  • Share repurchases and dividends were not reported.
  • Formal financial guidance for revenue, gross margin, operating expenses, or tax rate was not reported.
  • Prior-quarter comparisons were not reported.
  • Percentage year-over-year changes were not reported for the financial statement line items.
  • No reportable operating-segment revenue was disclosed.

Written by an AI language model from the company’s SEC earnings filing (Form 8-K Item 2.02, or Form 6-K for a foreign private issuer). Every figure is checked against the filing text, and a metric the filing does not print, or whose value, prior period and change do not add up, is dropped from the metrics. The model can still misread a table, in the metrics or in the text, so check a number in the filing before you rely on it. Consensus estimates, price targets and share-price reactions are not shown because they are not in the filing. AI-generated research, not investment advice.

second quarter 2026

AlphAI · Earnings readARCT · second quarter 2026 · ended June 30, 2026

Arcturus Therapeutics Announces Second Quarter 2026 Financial Results and Pipeline Progress

→Mixed quarter

ARCT-032 enrollment remained on schedule and ARCT-810 completed enrollment and dosing, while revenue declined to $3.0 million from $28.3 million and net loss widened to $23.8 million from $9.2 million. The CSL Seqirus settlement adds a $12 million cash payment and approximately $16 million of released liabilities and R&D credits, alongside cash runway through year end 2028.

Revenue
$3M
EPS · GAAP
$0.84

Key metrics

shortened, hover for the filing’s print
MetricValueq/qy/y
RevenueGAAP$3M––
Research and development expensesGAAP$17.5M––
General and administrative expensesGAAP$11M––
Net lossGAAP$23.8M––
Net loss per shareGAAP$0.84––
Six-month revenueGAAP$5M––
Six-month research and development expensesGAAP$39M––
Six-month general and administrative expensesGAAP$20.5M––
Six-month net lossGAAP$50.7M––
Six-month net loss per shareGAAP$1.79––

Q3 2026, Q4 2026 and year end 2028 outlook

  • NoteData and the regulatory plan for ARCT-810 is expected to be communicated later this quarter.
  • NoteThe decision to advance ARCT-032 into Phase 3 is expected in Q4 2026.
  • Notecash runway of over two and a half years through year end 2028

What drove it

  • Revenue decreases were primarily attributable to lower revenue recognized under the CSL Seqirus collaboration as the Company progressed toward termination of the agreement and regaining rights to KOSTAIVE® and its broader infectious disease vaccine portfolio.
  • Research and development expense decreases were primarily driven by lower research and development spending, including reduced salaries, wages, benefits and facilities costs.
  • ARCT-032 enrollment is advancing as expected, with active screening and enrollment in the U.S., Israel, and Turkey.
  • ARCT-810 completed enrollment of the ongoing Phase 2 study, and all enrolled subjects completed study drug dosing.
  • The Thermo Fisher Scientific collaboration will provide Phase 3 manufacturing, clinical research, and related services for ARCT-032.

Concerns

  • Revenue was lower due to reduced revenue recognized under the CSL Seqirus collaboration.
  • Net loss was higher than the comparable period last year.
  • The decision to advance ARCT-032 into Phase 3 depends on Phase 2 progress and is expected in Q4 2026.
  • ARCT-810 supplementary data evaluation and regulatory discussions remain pending.
  • Future value realization for KOSTAIVE® and the broader infectious disease vaccine portfolio depends on development, commercialization, and partnering opportunities.

What to watch

  • ARCT-810 data and the regulatory plan expected later this quarter.
  • The expected Q4 2026 decision on advancing ARCT-032 into Phase 3.
  • ARCT-032 Phase 2 enrollment progress and evidence of early clinical benefit, including ppFEV1, lung clearance index, quality-of-life measures, and HRCT imaging.
  • The Company’s evaluation of development, commercialization, and partnering opportunities for KOSTAIVE® and the infectious disease vaccine portfolio.
  • Cash runway through year end 2028 and clinical-development spending.

Balance sheet and cash flow

  • Cash and cash equivalents were $191.5 million as of June 30, 2026.
  • Cash and cash equivalents were $230.9 million on December 31, 2025.
  • Cash and cash equivalents decreased by $39.4 million.
  • CSL Seqirus will make a one-time cash payment of $12 million to Arcturus.
  • Arcturus will be released from liabilities associated with an R&D credit with an aggregate value of approximately $16 million.

Analysis

Arcturus reported a quarter marked by clinical execution and sharply lower collaboration revenue. Revenue was $3.0 million, compared with $28.3 million in the comparable period last year, as revenue recognized under the CSL Seqirus collaboration declined while the parties moved toward termination of their agreement. The Company reported a net loss of $23.8 million, compared with a net loss of $9.2 million in the comparable period last year, and net loss per share was $0.84 compared with $0.34.

Operating spending was lower in research and development but general and administrative expense was modestly higher. Research and development expenses were $17.5 million, compared with $29.6 million, primarily reflecting lower research and development spending and reduced salaries, wages, benefits and facilities costs. General and administrative expenses were $11.0 million, compared with $10.3 million, with legal fees contributing to the increase partly offset by reduced salaries, wages, benefits and facilities costs. The reported expense pattern reflects prioritization of the ARCT-032 cystic fibrosis and ARCT-810 OTC deficiency programs.

Pipeline milestones are the central operating catalysts. ARCT-032 remains in an open-label Phase 2 study, with active screening and enrollment in the U.S., Israel, and Turkey, and the Company expects a decision on advancing into Phase 3 in Q4 2026. ARCT-810 has completed Phase 2 enrollment and dosing for all enrolled subjects; the Company expects to communicate data and a regulatory plan later this quarter. Thermo Fisher will provide Phase 3 manufacturing, clinical research, and related services for ARCT-032 if Phase 2 produces positive results.

The CSL Seqirus termination and settlement agreement changes the portfolio and financial backdrop. Arcturus regained global rights to KOSTAIVE® and the broader infectious disease vaccine portfolio, subject to existing arrangements with Meiji Seika Pharma for the 2026-2027 season in Japan. CSL Seqirus will make a one-time cash payment of $12 million, and Arcturus will be released from liabilities associated with an R&D credit with an aggregate value of approximately $16 million. The Company ended June 30, 2026 with cash and cash equivalents of $191.5 million, down from $230.9 million on December 31, 2025, and stated cash runway of over two and a half years through year end 2028.

The key tension is that collaboration revenue has fallen materially while the Company evaluates how to maximize the value of the returned vaccine assets and prepares for potential late-stage investment in ARCT-032. Investors will focus on ARCT-810 data and regulatory planning later this quarter, the Q4 2026 ARCT-032 Phase 3 decision, and the Company’s ability to sustain disciplined capital allocation while pursuing rare-disease milestones.

Management, verbatim

We are encouraged by the continued progress of our ARCT-032 Phase 2 cystic fibrosis study, with active screening and ongoing enrollment across sites in the United States, Israel, and Turkey. With dosing completed of all subjects in our ARCT-810 Phase 2 OTC deficiency study, we look forward to sharing the data and regulatory plan later this quarter.

Joseph Payne, President & CEO of Arcturus

The CSL Seqirus termination and settlement agreement strengthens our financial position, and the Thermo Fisher collaboration supports execution of late-stage development for our CF program. We continue to maintain a strong balance sheet and cash runway of over two and a half years through year end 2028, allowing our company to reach important clinical and regulatory milestones for its rare disease pipeline.

Dennis Mulroy, Chief Financial Officer of Arcturus

Not in the filing

stated, not guessed
  • Gross profit and gross margin
  • Operating income or loss
  • Non-GAAP financial measures
  • Prior-quarter comparisons for reported financial metrics
  • Reported percentage year-over-year changes for revenue, expenses, net loss, and net loss per share
  • Cash flow from operations
  • Free cash flow
  • Debt
  • Share repurchases
  • Dividends
  • Financial revenue guidance
  • Gross-margin guidance
  • Operating-expense guidance
  • Tax-rate guidance
  • Reportable segment revenue

Written by an AI language model from the company’s SEC earnings filing (Form 8-K Item 2.02, or Form 6-K for a foreign private issuer). Every figure is checked against the filing text, and a metric the filing does not print, or whose value, prior period and change do not add up, is dropped from the metrics. The model can still misread a table, in the metrics or in the text, so check a number in the filing before you rely on it. Consensus estimates, price targets and share-price reactions are not shown because they are not in the filing. AI-generated research, not investment advice.

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