Breakdown | |||||
TTM | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 | Dec 2019 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
0.00 | 1.16M | 6.65M | 33.97M | 2.70M | 1.67M | Gross Profit |
-244.00K | 578.00K | 4.05M | 24.43M | 2.70M | 1.67M | EBIT |
-60.99M | -92.10M | -39.23M | -36.69M | -130.26M | -109.94M | EBITDA |
-53.36M | -86.50M | -38.85M | -86.22M | -121.36M | -103.63M | Net Income Common Stockholders |
-49.66M | -112.96M | -42.81M | -37.56M | -128.69M | -103.92M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
256.13M | 82.65M | 43.89M | 32.25M | 217.43M | 262.39M | Total Assets |
310.96M | 306.12M | 61.77M | 35.15M | 263.74M | 310.57M | Total Debt |
23.98M | 1.32M | 44.73M | 4.97M | 15.44M | 0.00 | Net Debt |
-224.14M | -37.95M | 838.00K | -27.27M | -201.99M | -53.77M | Total Liabilities |
44.70M | 233.13M | 192.49M | 124.36M | 67.74M | 52.06M | Stockholders Equity |
266.25M | 72.99M | -130.71M | -89.21M | 196.00M | 258.51M |
Cash Flow | Free Cash Flow | ||||
-77.94M | -96.46M | -13.44M | -33.14M | -98.06M | -113.19M | Operating Cash Flow |
-77.86M | -96.23M | -10.96M | -32.98M | -94.33M | -91.36M | Investing Cash Flow |
51.64M | 101.33M | -2.47M | -157.00K | 204.90M | -51.80M | Financing Cash Flow |
94.83M | 184.00K | 30.07M | 20.11M | 53.09M | 158.21M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
64 Neutral | $128.40B | ― | -3.15% | ― | 11.64% | -114.72% | |
49 Neutral | $6.90B | -0.08 | -53.01% | 2.43% | 24.84% | -3.06% | |
49 Neutral | $30.91B | ― | -414.62% | ― | 22.97% | 38.54% | |
48 Neutral | $3.72B | ― | -19.20% | ― | -89.95% | -123.71% | |
42 Neutral | $129.44M | ― | -98.10% | ― | -58.64% | -40.05% | |
39 Underperform | $962.71M | ― | -54.00% | ― | 59.55% | 3.09% | |
36 Underperform | $23.14M | ― | -93.26% | ― | -100.00% | 83.27% |
Q32 Bio announced updates to its corporate presentation, highlighting the progress in clinical trials for its lead products. The company is advancing its bempikibart program, demonstrating potential in treating alopecia areata with durable effects and favorable safety, and plans to initiate a Phase 2a Part B trial. Additionally, ADX-097 is being tested in a Phase 2 renal basket trial, with multiple data readouts expected in 2025, positioning Q32 for significant growth opportunities.
Q32 Bio announced encouraging results from its SIGNAL-AA Phase 2a trial for bempikibart in treating alopecia areata, demonstrating clinical activity and a favorable safety profile, prompting plans to expand the trial. However, its SIGNAL-AD trial for atopic dermatitis did not meet its primary endpoint, leading the company to plan a review of the results.