| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 35.77M | 47.98M | 103.78M | 48.58M | 3.07M | 9.33M |
| Gross Profit | -72.47M | -48.78M | 52.34M | 48.58M | 3.07M | -57.67M |
| EBITDA | -45.15M | -72.48M | 27.15M | -42.94M | -87.17M | -78.35M |
| Net Income | -43.84M | -68.57M | 22.81M | -46.41M | -89.76M | -78.28M |
Balance Sheet | ||||||
| Total Assets | 54.17M | 110.54M | 182.39M | 124.80M | 171.07M | 153.45M |
| Cash, Cash Equivalents and Short-Term Investments | 48.62M | 52.89M | 76.33M | 109.11M | 146.40M | 126.91M |
| Total Debt | 3.35M | 4.30M | 5.54M | 6.65M | 7.33M | 7.84M |
| Total Liabilities | 27.68M | 64.42M | 75.50M | 48.87M | 82.78M | 21.41M |
| Stockholders Equity | 26.49M | 46.12M | 106.89M | 75.93M | 88.29M | 132.04M |
Cash Flow | ||||||
| Free Cash Flow | -27.67M | -23.44M | -32.99M | -7.73M | 0.00 | -86.03M |
| Operating Cash Flow | -27.67M | -23.44M | -32.99M | -7.73M | -64.35M | -85.87M |
| Investing Cash Flow | 0.00 | 0.00 | 0.00 | 33.81M | 7.67M | 10.47M |
| Financing Cash Flow | 0.00 | 0.00 | 221.00K | -29.55M | 84.05M | 130.88M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
53 Neutral | $121.87M | -7.84 | ― | ― | ― | ― | |
52 Neutral | $172.89M | -2.35 | -260.65% | ― | ― | 3.70% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $141.41M | ― | -95.29% | ― | -67.38% | -1076.54% | |
50 Neutral | $429.59M | -5.25 | -30.40% | ― | ― | -100.71% | |
44 Neutral | $163.98M | -0.94 | -96.44% | ― | ― | 46.68% | |
42 Neutral | $84.76M | -0.93 | -63.46% | ― | ― | 21.61% |
On December 19, 2025, Spero Therapeutics reported that its partner GlaxoSmithKline resubmitted a New Drug Application to the U.S. Food and Drug Administration for tebipenem HBr, an oral carbapenem antibiotic candidate for the treatment of complicated urinary tract infections, including pyelonephritis. The resubmission activates a $25 million milestone payment to Spero under its license agreement with GSK, strengthening the company’s near-term cash position and underscoring the strategic importance of tebipenem HBr within its pipeline and its broader positioning in the anti-infectives market, while the program’s ultimate commercial and regulatory outcomes remain subject to significant clinical, regulatory, and execution risks.
The most recent analyst rating on (SPRO) stock is a Hold with a $4.00 price target. To see the full list of analyst forecasts on Spero Therapeutics stock, see the SPRO Stock Forecast page.
On November 13, 2025, Spero Therapeutics announced its third-quarter financial results and provided a business update. The company highlighted the Phase 3 PIVOT-PO trial results for tebipenem HBr, an investigational oral antibiotic for complicated urinary tract infections, which demonstrated non-inferiority to intravenous treatments. Spero’s partner, GSK, plans to submit these results to the FDA in the fourth quarter of 2025. The company reported a net loss of $7.4 million for the third quarter of 2025, a decrease from the previous year, and expects its current cash reserves to fund operations into 2028.
The most recent analyst rating on (SPRO) stock is a Hold with a $4.00 price target. To see the full list of analyst forecasts on Spero Therapeutics stock, see the SPRO Stock Forecast page.