Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
0.00 | 0.00 | 654.00K | 1.66M | 518.48K | Gross Profit |
0.00 | -1.84M | -491.00K | 1.64M | 518.48K | EBIT |
0.00 | -68.51M | -60.51M | -50.64M | -4.59M | EBITDA |
0.00 | -66.67M | -58.04M | -50.62M | -4.58M | Net Income Common Stockholders |
-98.33M | -66.39M | -59.28M | -50.62M | -5.15M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
121.52M | 121.47M | 77.33M | 135.86M | 29.37M | Total Assets |
146.94M | 139.81M | 97.08M | 136.86M | 29.41M | Total Debt |
9.92M | 11.64M | 13.48M | 0.00 | 3.01M | Net Debt |
-25.09M | -109.83M | -63.85M | -135.86M | -26.36M | Total Liabilities |
30.10M | 26.27M | 210.03M | 192.46M | 34.95M | Stockholders Equity |
116.84M | 113.53M | -112.95M | -55.60M | -5.54M |
Cash Flow | Free Cash Flow | |||
-81.63M | -59.66M | -55.46M | -44.37M | -3.13M | Operating Cash Flow |
-81.15M | -59.50M | -54.56M | -44.18M | -3.13M | Investing Cash Flow |
-94.08M | -165.00K | -901.00K | -188.00K | 0.00 | Financing Cash Flow |
88.78M | 103.79M | 189.00K | 150.86M | 32.38M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
52 Neutral | $5.28B | 3.75 | -42.72% | 2.86% | 17.70% | 2.03% | |
44 Neutral | $75.60M | ― | -138.71% | ― | ― | 20.91% | |
38 Underperform | $154.03M | ― | -85.37% | ― | ― | -24.18% | |
36 Underperform | $64.81M | ― | -45.60% | ― | ― | -57.45% | |
35 Underperform | $65.75M | ― | -125.38% | ― | ― | -10.99% | |
28 Underperform | $77.81M | ― | -2355.27% | ― | -100.00% | 52.65% |
On April 7, 2025, Lexeo Therapeutics announced positive interim results from their Phase 1/2 clinical trial of LX2006, a potential first-in-class treatment for Friedreich ataxia cardiomyopathy. The data showed significant improvements in cardiac biomarkers, including a 25% reduction in Left Ventricular Mass Index (LVMI) among participants with abnormal baseline levels, and demonstrated the treatment’s safety and efficacy. This progress aligns with FDA guidelines for an accelerated approval pathway, positioning Lexeo to initiate a registrational study by late 2025 or early 2026.