Breakdown | |||||
TTM | Mar 2024 | Mar 2023 | Mar 2022 | Mar 2021 | Mar 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
0.00 | 0.00 | 574.25K | 294.17K | 659.10K | 650.19K | Gross Profit |
-171.89K | -359.06K | 308.94K | 139.95K | 659.10K | 650.19K | EBIT |
-9.82M | -12.64M | -11.90M | -10.42M | -7.89M | -5.93M | EBITDA |
-9.37M | -11.85M | -11.66M | -10.30M | -7.85M | -6.30M | Net Income Common Stockholders |
-9.56M | -12.21M | -12.03M | -10.42M | -7.89M | -6.37M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
67.95K | 5.44M | 14.53M | 17.07M | 9.86M | 9.60M | Total Assets |
646.00K | 8.25M | 17.51M | 19.42M | 10.67M | 10.39M | Total Debt |
1.92M | 940.32K | 1.21M | 729.41K | 42.54K | 141.10K | Net Debt |
1.85M | -4.50M | -13.32M | -16.34M | -9.82M | -9.46M | Total Liabilities |
5.05M | 2.48M | 2.44M | 2.43M | 1.38M | 1.11M | Stockholders Equity |
-4.40M | 5.77M | 15.06M | 17.13M | 9.43M | 9.41M |
Cash Flow | Free Cash Flow | ||||
-5.98B | -10.38M | -11.45M | -10.12M | -6.82M | -5.35M | Operating Cash Flow |
-5.98B | -10.13M | -10.51M | -9.77M | -6.76M | -5.20M | Investing Cash Flow |
-2.20M | -250.87K | -943.11K | -349.19K | -59.88K | -151.66K | Financing Cash Flow |
5.41M | 1.29M | 8.91M | 17.37M | 7.13M | 11.13M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
48 Neutral | $6.36B | 1.14 | -49.00% | 2.63% | 17.14% | 1.39% | |
43 Neutral | $6.36M | ― | -18.06% | ― | -30.19% | 75.92% | |
43 Neutral | $9.11M | ― | -170.33% | ― | -14.79% | 76.94% | |
42 Neutral | $9.06M | ― | -809.29% | ― | ― | ― | |
35 Underperform | $6.14M | ― | 77.20% | ― | -3.76% | 39.52% | |
34 Underperform | $6.80M | ― | -21.59% | ― | ― | 71.57% | |
23 Underperform | $7.24M | ― | -160.04% | ― | -100.00% | 68.26% |
In its recent financial release, Aethlon Medical reported a significant milestone in its oncology trials in Australia, announcing the first patient treated with the Hemopurifier for solid tumors not responding to anti-PD-1 antibodies on January 29, 2025. The company has also implemented strategic cost-cutting measures, reducing operating expenses by 50% from the previous year, and made protocol amendments to accelerate trial timelines and improve patient enrollment. These developments are crucial for enhancing the company’s clinical program efficiency and potentially improving therapeutic responses in future oncology efficacy trials.