Arcturus Therapeutics Holdings

ARCTNASDAQUSD

THESIS ALERT

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$9.31
−$0.08 (−0.85%)Today 1M −31.66%
After hours$9.310.00%

Updated Nov 11, 4:00 PM ET · Regular session · May be delayed

Source valuation snapshot. Not a live recalculation.
Latest filed annual earnings; price snapshot date unavailable. Not forward P/E.
Diluted earnings per share from the latest filed annual.
$9.39
Prior regular-session close from the quote source.
$9.14–$9.67
Regular-session low and high so far today.
443.2K
Regular-session shares traded · Nov 11, 4:00 PM ET.
Not yet confirmed
The company has not confirmed its next report date. Reported quarters are available in the chart’s Earnings view.
$5.50–$17.96
52-week trading low and high returned by the quote source.

Understand the Business

Why the Stock Moved

Period-matched expectations history is not yet available. Current metrics are not a substitute for a historical explanation.

The core investment thesis

Own ARCT if Arcturus is a high-risk mRNA platform option whose value depends on turning validated self-amplifying vaccine technology into repeat-dose rare-disease therapeutics before COVID-vaccine economics and cash runway fade.

ARCT price history

Latest price$9.31Today−$0.08 (-0.85%)
ARCT -27.44%S&P 500 -2.42%Since first plotted close
4 hours

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Investment thesis

What must happen next

3 MATERIAL PROPOSITIONS
  • KOSTAIVE gives Arcturus real-world regulatory and commercial validation for self-amplifying mRNA, but that validation only creates durable value if CSL Seqirus and Meiji can keep the product relevant despite declining COVID demand.HoldingMateriality: High

    Item 1 and MD&A state KOSTAIVE is the world’s first approved self-amplifying mRNA vaccine and has approval in Japan, the European Union and the United Kingdom. If KOSTAIVE remains commercially useful, it helps fund and validate the platform; if partner economics fade, Arcturus becomes almost entirely dependent on unproven clinical assets.

    Watch: CSL Limited reported an approximately $430 million write-down attributable to the CSL Seqirus collaboration, citing declining COVID-19 disease burden and more onerous U.S. regulatory requirements.

    Supporting sources

    Source notes are factual paraphrases; read the original disclosures below.

    Item 1 and MD&A state KOSTAIVE is the world’s first approved self-amplifying mRNA vaccine and has approval in Japan, the.

    Open source ↗
  • Arcturus’ balance-sheet value depends on having enough cash to reach ARCT-032 and ARCT-810 clinical/regulatory inflections without being forced into unfavorable financing.StrengtheningMateriality: High

    Cash and cash equivalents were $230.909 million at December 31, 2025. If cash carries the company to meaningful data, shareholders keep the upside; if trials expand before validation, dilution or strategic concessions could absorb much of the option value.

    Watch: ARCT-032 or ARCT-810 requires larger, longer, or repeated trials before producing decision-quality efficacy data.

    Supporting sources

    Source notes are factual paraphrases; read the original disclosures below.

    Cash and cash equivalents were $230.909 million at December 31, 2025.

    Open source ↗
  • The core platform claim is that LUNAR delivery and mRNA construct design can support repeat dosing in disease-relevant tissues; ARCT-032 and ARCT-810 must show this is therapeutically useful, not merely tolerable in small early studies.HoldingMateriality: Medium

    Item 1 and MD&A describe LUNAR as intended to address the major hurdle in RNA drug development: effective and safe delivery of RNA to disease-relevant target tissues. Successful repeat dosing would expand Arcturus from vaccine validation into higher-value rare-disease therapeutics; failure would shrink the company back to a weakened vaccine-collaboration story.

    Watch: The 12-week ARCT-032 CF study shows dose-limiting tolerability problems, bronchospasm, or no meaningful preliminary efficacy.

    Supporting sources

    Source notes are factual paraphrases; read the original disclosures below.

    Item 1 and MD&A describe LUNAR as intended to address the major hurdle in RNA drug development: effective and safe.

    Open source ↗
Full investment case & evidence

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Original research

KOSTAIVE gives Arcturus real-world regulatory and commercial validation for self-amplifying mRNA, but that validation only creates durable value if CSL Seqirus and Meiji can keep the product relevant despite declining COVID demand. If KOSTAIVE remains commercially useful, it helps fund and validate the platform; if partner economics fade, Arcturus becomes almost entirely dependent on unproven clinical assets.

Arcturus’ balance-sheet value depends on having enough cash to reach ARCT-032 and ARCT-810 clinical/regulatory inflections without being forced into unfavorable financing. If cash carries the company to meaningful data, shareholders keep the upside; if trials expand before validation, dilution or strategic concessions could absorb much of the option value.

The core platform claim is that LUNAR delivery and mRNA construct design can support repeat dosing in disease-relevant tissues; ARCT-032 and ARCT-810 must show this is therapeutically useful, not merely tolerable in small early studies. Successful repeat dosing would expand Arcturus from vaccine validation into higher-value rare-disease therapeutics; failure would shrink the company back to a weakened vaccine-collaboration story.

All standing thesis claims
Original report summary

Arcturus is a high-risk mRNA platform option whose value depends on turning validated self-amplifying vaccine technology into repeat-dose rare-disease therapeutics before COVID-vaccine economics and cash runway fade.

Evidence assessed Nov 9, 2026. Expand each conclusion for its evidence and what would change it. Thesis evidence—not a buy or sell recommendation.

Bull case and bear case

Bull case and bear case for Arcturus Therapeutics Holdings

Where the evidence on Arcturus Therapeutics Holdings stands: Holding on the latest evidence (Nov 9, 2026). Of its 3 thesis points, 1 strengthening and 2 holding.

Bull case: what the evidence supports

  • KOSTAIVE gives Arcturus real-world regulatory and commercial validation for self-amplifying mRNA, but that validation only creates durable value if CSL Seqirus and Meiji can keep the product relevant despite declining COVID demand.

    sec.gov ↗

  • Arcturus’ balance-sheet value depends on having enough cash to reach ARCT-032 and ARCT-810 clinical/regulatory inflections without being forced into unfavorable financing.

    sec.gov ↗

  • The core platform claim is that LUNAR delivery and mRNA construct design can support repeat dosing in disease-relevant tissues; ARCT-032 and ARCT-810 must show this is therapeutically useful, not merely tolerable in small early studies.

    sec.gov ↗

Bear case: what would count against it

  • CSL Limited reported an approximately $430 million write-down attributable to the CSL Seqirus collaboration, citing declining COVID-19 disease burden and more onerous U.S. regulatory requirements.

    sec.gov ↗

  • ARCT-032 or ARCT-810 requires larger, longer, or repeated trials before producing decision-quality efficacy data.

    sec.gov ↗

  • The 12-week ARCT-032 CF study shows dose-limiting tolerability problems, bronchospasm, or no meaningful preliminary efficacy.

    sec.gov ↗

Thesis-Break Engine

Thesis-break watch · Arcturus Therapeutics Holdings

Loading the break-condition record for Arcturus Therapeutics Holdings.

How the Thesis-Break Engine works →Historical outcomes are measured against the market after past breaks of the same kind, across all companies. Not a prediction.

MARKET + FINANCIAL SNAPSHOT

The numbers behind the thesis

Sourced from filings and market data

What Changed

  1. Mixed
    Reported results of operations (earnings release).

    Arcturus Therapeutics Holdings filed an SEC 8-K on 2026-11-05: Reported results of operations (earnings release). It is a dated development that tests the current thesis.

  2. Mixed
    Regulation FD disclosure.

    Arcturus Therapeutics Holdings filed an SEC 8-K on 2026-09-23: Regulation FD disclosure. It is a dated development that tests the current thesis.

  3. Mixed
    Regulation FD disclosure.

    Arcturus Therapeutics Holdings filed an SEC 8-K on 2026-08-25: Regulation FD disclosure. It is a dated development that tests the current thesis.

Risks / falsifiers

What could break the thesis

  • CSL Limited reported an approximately $430 million write-down attributable to the CSL Seqirus collaboration, citing declining COVID-19 disease burden and more onerous U.S. regulatory requirements.
  • ARCT-032 or ARCT-810 requires larger, longer, or repeated trials before producing decision-quality efficacy data.
  • The 12-week ARCT-032 CF study shows dose-limiting tolerability problems, bronchospasm, or no meaningful preliminary efficacy.

ARCT news

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Financial statements

ARCT income statement

Annual filed results · USD · Oldest to newest. Margins are calculated from the reported figures.

ARCT: quick answers

Which well-known investors own ARCT?
1 of the 37 well-known funds tracked here reported ARCT shares in their latest 13F filing. By share of the fund's portfolio: ARK Investment Management (Cathie Wood), 0.1%. Fund portfolios

ARCT in well-known investors’ portfolios

1 of 37 funds reported ARCT shares in their latest 13F filing. A 13F shows quarter-end positions and arrives up to 45 days later.

FundOf its portfolioValueChangeQuarter
Cathie WoodARK Investment Management0.13%$19.5M+4.8%Q2 2026

Every fund’s portfolio

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