Breakdown | Jun 2024 | Jun 2023 | Jun 2022 | Jun 2021 | Jun 2020 |
---|---|---|---|---|---|
Income Statement | |||||
Total Revenue | 9.93M | 4.89M | 3.64M | 1.98M | 3.52M |
Gross Profit | 9.93M | 4.48M | 3.24M | 1.60M | 3.10M |
EBITDA | -12.92M | -15.22M | -12.72M | -5.35M | -8.20M |
Net Income | -13.04M | -10.75M | -9.50M | -3.92M | -5.33M |
Balance Sheet | |||||
Total Assets | 21.31M | 15.21M | 23.31M | 18.38M | 11.94M |
Cash, Cash Equivalents and Short-Term Investments | 9.45M | 8.46M | 16.37M | 13.42M | 5.04M |
Total Debt | 319.07K | 86.93K | 165.27K | 236.44K | 389.87K |
Total Liabilities | 1.62M | 1.80M | 1.57M | 920.32K | 1.05M |
Stockholders Equity | 19.70M | 13.41M | 21.74M | 17.46M | 10.89M |
Cash Flow | |||||
Free Cash Flow | -16.96M | -8.73M | -9.52M | -1.73M | -2.88M |
Operating Cash Flow | -16.95M | -8.70M | -9.52M | -1.72M | -2.86M |
Investing Cash Flow | -8.16K | -36.60K | -2.94K | -6.19K | -22.76K |
Financing Cash Flow | 17.95M | 824.62K | 12.42M | 10.11M | 282.26K |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
76 Outperform | AU$104.25M | 11.43 | 45.86% | 1.81% | 71.65% | 152.89% | |
56 Neutral | AU$33.82M | ― | -36.95% | ― | ― | 11.11% | |
52 Neutral | AU$73.07M | ― | -55.44% | ― | ― | 49.25% | |
50 Neutral | AU$2.51B | 3.43 | -57.47% | 2.67% | 36.73% | 13.67% | |
49 Neutral | $100.40M | ― | -154.88% | ― | ― | 20.00% | |
40 Underperform | AU$124.80M | ― | -85.35% | ― | 315.11% | 51.16% | |
34 Underperform | AU$52.03M | ― | -108.26% | ― | ― | 53.41% |
Actinogen Medical has secured up to $13.8 million in non-dilutive funding through a Research and Development Tax Incentive, with an initial $3 million received and further amounts contingent on future approvals. This funding will support the ongoing XanaMIA phase 2b/3 Alzheimer’s disease trial and general working capital, strengthening the company’s financial position as it progresses toward key milestones, including interim analysis of its clinical trial.
Actinogen Medical has reached a significant milestone in its XanaMIA phase 2b/3 trial for Alzheimer’s disease by enrolling its 100th participant, setting the stage for an interim analysis of safety and efficacy data. This analysis, conducted by an independent Data Monitoring Committee, will occur in January 2026, with final trial results expected in late 2026. The trial aims to demonstrate the safety and efficacy of Xanamem, potentially expediting its regulatory approval. The company is also preparing for discussions with the US FDA regarding approval pathways and may seek commercial partnerships for the next phase of development.
Actinogen Medical Limited has announced that BVF Partners L.P., along with its affiliates, has ceased to be a substantial holder in the company. This development follows a series of on-market sales of fully paid ordinary shares by BVF Partners and its associates, which took place between April 22 and May 19, 2025. The divestment of shares by BVF Partners may impact Actinogen Medical’s shareholder composition and could influence market perceptions of the company’s stock.
Actinogen Medical announced positive results from a Phase 2 trial of its drug Xanamem, presented at the American Psychiatric Association’s 2025 meeting. The trial demonstrated that a 10 mg dose of Xanamem significantly improves symptoms of moderate Major Depressive Disorder, validating its mechanism of controlling brain cortisol levels. These findings not only highlight Xanamem’s potential as an effective antidepressant with a unique mechanism of action but also support its use in ongoing trials for Alzheimer’s Disease. The promising safety profile and durability of Xanamem’s benefits position it as a competitive candidate in the antidepressant market, potentially benefiting patients with Alzheimer’s who also suffer from depression.
Actinogen Medical announced a panel discussion featuring key company figures and experts to discuss advancements in Alzheimer’s treatments and the commercialization of Xanamem, their novel oral medication. The company is actively preparing for commercialization by designing pivotal trials, developing thought leaders, and refining communication strategies, which are crucial for maximizing future partnerships and addressing the significant unmet medical need for effective Alzheimer’s therapies.
Actinogen Medical has made significant progress in its XanaMIA phase 2b/3 clinical trial for Alzheimer’s disease, with accelerated patient screening and enrollment across multiple sites in the US and Australia. The company also achieved a successful regulatory meeting with the FDA regarding major depressive disorder, marking a major accomplishment that could enhance future partnerships and funding opportunities. Additionally, the World Health Organization granted a unique name to Xanamem, recognizing its novel mechanism of action, and the company continues to advance its manufacturing and strategic planning efforts.
Actinogen Medical announced an upcoming Clinical Trials Science Forum to discuss advancements in Alzheimer’s treatments and the commercialization of Xanamem, their novel oral medication. The forum will highlight the company’s strategic planning for commercialization, including trial designs and stakeholder engagement, which are crucial for maximizing future partnerships and addressing the unmet need for effective Alzheimer’s therapies.
Actinogen Medical Limited has seen a change in the interests of its substantial holder, BVF Partners L.P., which has reduced its voting power from 7.29% to 6.24% through a series of on-market sales of fully paid ordinary shares. This change in holdings may impact Actinogen’s market position and shareholder dynamics, as BVF Partners L.P. adjusts its investment strategy in the company.