Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 117.50M | 138.39M | 157.75M | 205.75M | 12.36M | 9.54M |
Gross Profit | 52.92M | 134.84M | 154.79M | 58.25M | -161.40M | -46.41M |
EBITDA | -55.32M | -77.40M | -24.17M | 13.70M | -201.66M | -70.64M |
Net Income | -60.16M | -80.94M | -29.73M | 9.35M | -203.67M | -72.15M |
Balance Sheet | ||||||
Total Assets | 309.27M | 344.07M | 429.40M | 450.39M | 392.81M | 476.46M |
Cash, Cash Equivalents and Short-Term Investments | 196.47M | 237.03M | 292.00M | 391.88M | 370.49M | 462.89M |
Total Debt | 22.93M | 28.55M | 30.22M | 94.75M | 69.15M | 20.75M |
Total Liabilities | 78.22M | 103.09M | 150.89M | 180.07M | 164.60M | 79.90M |
Stockholders Equity | 231.05M | 240.98M | 278.51M | 270.31M | 228.21M | 396.55M |
Cash Flow | ||||||
Free Cash Flow | -64.67M | -60.40M | -21.00M | 24.27M | -138.45M | -44.60M |
Operating Cash Flow | -5.78M | -59.75M | -18.10M | 31.99M | -135.04M | -42.86M |
Investing Cash Flow | -219.45K | -648.00K | -2.90M | -7.73M | -3.41M | -1.74M |
Financing Cash Flow | 1.30M | 5.42M | -24.09M | -2.86M | 48.02M | 436.14M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
63 Neutral | 988.10M | -5.73 | -128.35% | ― | -0.90% | -89.51% | |
58 Neutral | $490.14M | ― | -24.57% | ― | -26.88% | 13.41% | |
44 Neutral | 580.99M | -2.69 | 0.00% | ― | -78.63% | 1.88% | |
43 Neutral | 378.93M | -3.12 | 0.00% | ― | 0.00% | -9.14% | |
41 Neutral | 607.08M | -4.46 | 0.00% | ― | 0.00% | 39.03% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
On August 29, 2025, Meiji Seika Pharma Co., Ltd., a subsidiary of Meiji Holdings Co., Ltd., announced the approval in Japan for KOSTAIVE®, a self-amplifying mRNA COVID-19 vaccine. This vaccine targets the SARS-CoV-2 Omicron sub lineage JN.1 variant XEC and has shown efficacy against several other variants in non-clinical studies. The vaccine is supplied as a two-dose vial and distribution is set to begin in late September 2025. This development follows a distribution agreement with CSL Seqirus for the Japanese market, potentially strengthening the company’s position in the vaccine industry.
On June 30, 2025, Arcturus Therapeutics announced positive interim results from Phase 2 studies of ARCT-810, an mRNA therapeutic for treating OTC deficiency. The studies showed significant reductions in glutamine levels and improvements in urea cycle function, with ARCT-810 being safe and well tolerated. These findings suggest a promising path forward for addressing an unmet medical need in OTC deficiency, potentially leading to a pivotal study.
On June 6, 2025, Arcturus Therapeutics held its annual stockholders meeting where key proposals were voted on, including the election of nine directors to the Board, approval of executive compensation, and the ratification of Deloitte as the independent accounting firm for 2025. All proposals were approved, indicating strong shareholder support for the company’s leadership and strategic direction.