| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 107.27M | 105.76M | 113.45M | 102.29M | 7.34M | 20.95M |
| Gross Profit | 102.42M | 101.87M | 108.81M | 97.50M | -332.00K | 11.79M |
| EBITDA | 15.03M | 17.82M | 20.33M | 10.33M | -87.64M | -56.10M |
| Net Income | 6.65M | 12.09M | -92.93M | 2.30M | -87.93M | -55.54M |
Balance Sheet | ||||||
| Total Assets | 159.38M | 125.41M | 116.54M | 84.75M | 55.66M | 94.85M |
| Cash, Cash Equivalents and Short-Term Investments | 40.40M | 26.67M | 33.51M | 25.18M | 46.85M | 79.35M |
| Total Debt | 1.17M | 1.60M | 409.00K | 613.00K | 2.38M | 1.64M |
| Total Liabilities | 21.97M | 27.00M | 102.59M | 12.54M | 14.57M | 18.78M |
| Stockholders Equity | 101.92M | 63.32M | -15.83M | 42.52M | 41.09M | 76.07M |
Cash Flow | ||||||
| Free Cash Flow | 1.35M | -6.77M | 17.31M | 5.68M | -84.59M | -55.31M |
| Operating Cash Flow | 3.88M | -3.64M | 25.89M | 10.68M | -83.75M | -55.05M |
| Investing Cash Flow | -4.33M | -19.88M | -19.76M | -13.81M | 48.19M | 9.66M |
| Financing Cash Flow | 25.02M | 2.10M | 2.50M | 0.00 | 49.55M | 60.38M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
65 Neutral | $1.20B | ― | -30.16% | ― | 31.11% | -46.75% | |
61 Neutral | $3.95B | -36.03 | -29.12% | ― | ― | 12.45% | |
58 Neutral | $1.93B | -17.96 | -24.43% | ― | ― | -44.79% | |
57 Neutral | $770.33M | -3.81 | ― | ― | ― | -13.14% | |
57 Neutral | $1.56B | -15.53 | -34.75% | ― | ― | -17.01% | |
56 Neutral | $698.95M | 201.84 | 8.06% | ― | ― | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
On January 5, 2026, Gyre Therapeutics announced that its majority-owned Chinese subsidiary, Gyre Pharmaceuticals, had completed a Pre-New Drug Application communication meeting with China’s Center for Drug Evaluation, which agreed that existing Phase 3 data on Hydronidone support filing for conditional approval and eligibility for priority review in chronic hepatitis B–associated liver fibrosis, including early cirrhosis. The Phase 3 trial, whose topline results were disclosed on May 22, 2025, showed Hydronidone met its primary endpoint with significantly higher rates of fibrosis regression versus placebo and a favorable safety profile, and the company now plans an additional confirmatory Phase 3c outcomes study in China as part of a regulatory pathway that could accelerate Hydronidone’s entry into a large, underserved Chinese market of an estimated 2.6 million patients with clinically significant CHB-related liver fibrosis, potentially strengthening Gyre’s position in the liver fibrosis segment and broadening its commercial footprint in China.
The most recent analyst rating on (GYRE) stock is a Hold with a $8.50 price target. To see the full list of analyst forecasts on Gyre Therapeutics stock, see the GYRE Stock Forecast page.