Breakdown | |||||
TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
1.93M | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
1.59M | 0.00 | -399.00K | -1.01M | -345.00K | 0.00 | EBIT |
-88.43M | -89.68M | -88.87M | -68.88M | -42.41M | -6.29M | EBITDA |
-87.97M | -89.68M | -88.47M | -67.30M | -42.94M | -28.55M | Net Income Common Stockholders |
-82.60M | -84.26M | -82.64M | -67.73M | -43.25M | -28.55M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
24.15M | 97.80M | 117.94M | 186.60M | 91.42M | 24.15M | Total Assets |
25.30M | 117.69M | 140.86M | 200.39M | 102.44M | 25.30M | Total Debt |
303.00K | 12.95M | 13.85M | 176.00K | 937.00K | 303.00 | Net Debt |
-23.85M | -26.07M | -38.14M | -186.43M | -90.48M | -24.15M | Total Liabilities |
6.54M | 46.06M | 24.61M | 11.31M | 171.88M | 53.58M | Stockholders Equity |
18.75M | 71.64M | 116.25M | 189.08M | -69.44M | -28.28M |
Cash Flow | Free Cash Flow | ||||
-48.61M | -51.23M | -71.04M | -66.07M | -39.55M | -5.68M | Operating Cash Flow |
-48.59M | -51.22M | -70.36M | -65.15M | -39.35M | -5.18M | Investing Cash Flow |
11.59M | 8.76M | -65.14M | -921.00K | -204.00K | -500.00K | Financing Cash Flow |
25.11M | 29.49M | 888.00K | 161.25M | 107.75M | 29.83M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
67 Neutral | $20.37B | 12.74 | 10.36% | ― | -1.60% | 39.71% | |
59 Neutral | $36.55B | ― | -414.62% | ― | 22.97% | 38.54% | |
49 Neutral | $5.01B | ― | -93.03% | ― | -10.48% | -18.79% | |
49 Neutral | $6.88B | 0.82 | -52.97% | 2.48% | 20.92% | 1.17% | |
48 Neutral | $528.74M | ― | -63.37% | ― | -52.30% | 27.13% | |
41 Neutral | $2.01B | ― | -37.40% | ― | -100.00% | -144.79% | |
32 Underperform | $84.01M | ― | -89.69% | ― | ― | 3.01% |
On January 23, 2025, Vigil Neuroscience announced positive results from its completed Phase 1 clinical trial of VG-3927, a small molecule TREM2 agonist, aimed at treating Alzheimer’s disease. The trial demonstrated a favorable safety and tolerability profile, along with significant pharmacokinetic and pharmacodynamic markers, supporting the drug’s advancement to a Phase 2 trial scheduled for the third quarter of 2025. This development positions VG-3927 as a promising once-daily oral therapy that could offer a more convenient treatment option for Alzheimer’s patients, potentially addressing disease progression beyond targeting amyloid plaques.