Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 20.00K | 20.00K | 426.00K | -68.00K | 4.41M | 8.19M |
Gross Profit | -10.00K | 20.00K | -51.00K | -568.00K | -69.43M | -25.32M |
EBITDA | -89.10M | -94.81M | -87.94M | -84.40M | -96.53M | -54.15M |
Net Income | -87.75M | -95.06M | -88.45M | -84.71M | -97.09M | -49.04M |
Balance Sheet | ||||||
Total Assets | 190.35M | 139.31M | 210.64M | 206.93M | 218.86M | 245.12M |
Cash, Cash Equivalents and Short-Term Investments | 183.10M | 131.89M | 197.81M | 184.88M | 190.30M | 215.92M |
Total Debt | 15.85M | 1.68M | 671.00K | 1.12M | 1.53M | 1.82M |
Total Liabilities | 28.98M | 15.80M | 16.54M | 21.64M | 19.73M | 19.24M |
Stockholders Equity | 161.37M | 123.51M | 194.10M | 185.29M | 199.13M | 225.88M |
Cash Flow | ||||||
Free Cash Flow | -81.58M | -79.85M | -75.86M | -62.71M | -90.55M | -34.65M |
Operating Cash Flow | -81.57M | -79.85M | -75.81M | -62.59M | -78.24M | -34.44M |
Investing Cash Flow | 110.84M | -28.39M | 13.73M | -73.40M | 87.52M | -72.09M |
Financing Cash Flow | 96.71M | 10.04M | 86.11M | 56.78M | 65.10M | 213.49M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
68 Neutral | $1.08B | 23.15 | 18.17% | ― | 1218.82% | ― | |
60 Neutral | HK$19.22B | 4.48 | -1.43% | 3.30% | 11.19% | -15.58% | |
55 Neutral | $634.52M | ― | 344.74% | ― | -47.32% | -26.67% | |
51 Neutral | $319.49M | ― | -55.91% | ― | -95.11% | 27.25% | |
43 Neutral | $941.12M | ― | -43.82% | ― | ― | -7.33% | |
41 Neutral | $465.75M | ― | -52.18% | ― | 187.52% | 26.32% | |
33 Underperform | $856.10M | ― | -109.12% | ― | ― | 7.58% |
On June 26, 2025, Altimmune announced positive topline results from its IMPACT Phase 2b trial of pemvidutide for treating metabolic dysfunction-associated steatohepatitis (MASH). The trial showed significant MASH resolution and weight loss in participants treated with pemvidutide compared to placebo, with low discontinuation rates due to adverse events. These results suggest pemvidutide’s potential as a transformative therapy for MASH, a condition with limited current treatment options, and support further progression to Phase 3 trials.