Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 452.00K | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
Gross Profit | -12.00K | -453.00K | -399.00K | -1.01M | -345.00K | 0.00 |
EBITDA | -96.52M | -83.80M | -88.47M | -67.30M | -42.94M | -28.55M |
Net Income | -92.17M | -84.26M | -82.64M | -67.73M | -43.25M | -28.55M |
Balance Sheet | ||||||
Total Assets | 86.70M | 117.69M | 140.86M | 200.39M | 102.44M | 25.30M |
Cash, Cash Equivalents and Short-Term Investments | 66.98M | 97.80M | 117.94M | 186.60M | 91.42M | 24.15M |
Total Debt | 12.44M | 12.95M | 13.85M | 176.00K | 937.00K | 303.00 |
Total Liabilities | 45.44M | 46.06M | 24.61M | 11.31M | 171.88M | 53.58M |
Stockholders Equity | 41.26M | 71.64M | 116.25M | 189.08M | -69.44M | -28.28M |
Cash Flow | ||||||
Free Cash Flow | -58.57M | -51.23M | -71.04M | -66.07M | -39.55M | -5.68M |
Operating Cash Flow | -58.21M | -51.22M | -70.36M | -65.15M | -39.35M | -5.18M |
Investing Cash Flow | 24.28M | 8.76M | -65.14M | -921.00K | -204.00K | -500.00K |
Financing Cash Flow | 37.84M | 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 |
---|---|---|---|---|---|---|---|
52 Neutral | $186.25M | ― | -68.93% | ― | -72.45% | -28.60% | |
48 Neutral | $43.28M | ― | -150.50% | ― | -100.00% | 64.16% | |
47 Neutral | C$213.29M | -1.44 | -30.58% | 3.10% | 19.48% | -0.04% | |
45 Neutral | $407.33M | ― | -22.38% | ― | -100.00% | 72.51% | |
37 Underperform | $130.32M | ― | -120.11% | ― | ― | -32.50% | |
35 Underperform | $383.88M | ― | -145.68% | ― | ― | 3.01% | |
28 Underperform | $59.12M | ― | -3987.11% | ― | ― | 88.03% |
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.