| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 37.19M | 28.52M | 7.16M | 0.00 | 6.25M | 79.11M |
| Gross Profit | 6.79M | 28.52M | -41.74M | -69.08M | 6.25M | -22.23M |
| EBITDA | -41.63M | -45.29M | -64.20M | -92.52M | -90.58M | -58.40M |
| Net Income | -38.55M | -40.18M | -61.23M | -93.09M | -129.85M | -62.15M |
Balance Sheet | ||||||
| Total Assets | 240.00M | 119.17M | 136.82M | 101.79M | 191.06M | 283.25M |
| Cash, Cash Equivalents and Short-Term Investments | 232.56M | 112.08M | 130.25M | 91.61M | 146.63M | 216.41M |
| Total Debt | 2.75M | 3.09M | 2.34M | 3.46M | 6.48M | 10.13M |
| Total Liabilities | 57.30M | 85.81M | 95.73M | 19.13M | 22.13M | 42.68M |
| Stockholders Equity | 182.69M | 33.36M | 41.10M | 82.66M | 168.93M | 240.58M |
Cash Flow | ||||||
| Free Cash Flow | -55.78M | -51.15M | 22.49M | -84.56M | -96.49M | -65.18M |
| Operating Cash Flow | -55.74M | -51.12M | 22.74M | -84.46M | -93.40M | -62.96M |
| Investing Cash Flow | -141.39M | 40.17M | -69.14M | 90.64M | 26.52M | 68.07M |
| Financing Cash Flow | 191.21M | 29.45M | 13.82M | 614.00K | 53.06M | 7.60M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
53 Neutral | $557.71M | -7.34 | -36.94% | ― | 31.30% | 32.79% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $273.67M | -1.93 | -52.44% | ― | 40.20% | -4.07% | |
47 Neutral | $389.42M | -11.44 | -43.71% | ― | ― | 80.95% | |
38 Underperform | $755.42M | -3.83 | -80.69% | ― | ― | 4.97% | |
38 Underperform | $748.25M | -3.67 | -83.98% | ― | ― | -35.62% | |
33 Underperform | $271.91M | -0.03 | ― | ― | ― | -1072.48% |
On December 8, 2025, Assembly Biosciences announced positive interim results from Phase 1b clinical studies of its investigational herpes simplex virus (HSV) helicase-primase inhibitors, ABI-1179 and ABI-5366, for recurrent genital herpes. The studies demonstrated significant reductions in HSV-2 shedding rates and virologically confirmed genital lesion rates compared to placebo, with ABI-1179 showing a 98% reduction in shedding rate and ABI-5366 showing a 76% reduction. Both candidates were well-tolerated, and the company is progressing Phase 2 enabling activities for ABI-1179 and planning longer-duration Phase 2 studies for ABI-5366, potentially impacting their market positioning in the antiviral therapeutics sector.