| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 151.93M | 128.94M | 8.57M | 63.57M | 20.34M | 0.00 |
| Gross Profit | 124.03M | 107.93M | -313.00K | 63.57M | -261.66M | -244.65M |
| EBITDA | 30.50M | -75.75M | -266.00M | -222.26M | -331.12M | -300.72M |
| Net Income | 23.40M | -85.40M | -276.13M | -228.30M | -340.14M | -306.62M |
Balance Sheet | ||||||
| Total Assets | 30.17M | 109.10M | 165.50M | 376.42M | 468.13M | 588.12M |
| Cash, Cash Equivalents and Short-Term Investments | 13.71M | 42.50M | 51.73M | 242.82M | 371.07M | 500.66M |
| Total Debt | 58.60M | 43.83M | 57.87M | 71.70M | 28.27M | 15.03M |
| Total Liabilities | 66.80M | 206.38M | 264.74M | 249.78M | 188.51M | 125.78M |
| Stockholders Equity | -36.63M | -97.28M | -99.23M | 126.64M | 279.61M | 462.34M |
Cash Flow | ||||||
| Free Cash Flow | -69.80M | -68.96M | -194.20M | -274.62M | -231.10M | -185.27M |
| Operating Cash Flow | -69.71M | -68.72M | -192.98M | -270.43M | -220.52M | -180.76M |
| Investing Cash Flow | 13.08M | 8.62M | 123.87M | 202.96M | 22.26M | -120.73M |
| Financing Cash Flow | 15.77M | 59.28M | 2.01M | 53.08M | 103.94M | 427.57M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | $252.16M | -1.67 | -49.18% | ― | -33.76% | 17.54% | |
50 Neutral | $154.29M | -0.95 | ― | ― | -63.96% | -28.50% | |
49 Neutral | $66.40M | -1.05 | -76.44% | ― | -10.03% | 11.06% | |
48 Neutral | $113.23M | -1.45 | -81.13% | ― | -9.70% | 23.23% | |
46 Neutral | $42.40M | 1.99 | ― | ― | 51.27% | ― |
On January 12, 2026, Atara Biotherapeutics reported that the U.S. Food and Drug Administration issued a Complete Response Letter for EBVALLO (tabelecleucel), rejecting its Biologics License Application as a monotherapy for EBV-positive post-transplant lymphoproliferative disease in adults and children, despite previously resolving manufacturing compliance issues and raising no new safety concerns. The FDA, reversing its earlier stance, now deems the single-arm ALLELE trial inadequate to demonstrate effectiveness for accelerated approval, prompting Atara’s U.S. commercialization partner Pierre Fabre to seek a Type A meeting as the companies work to salvage a path forward for the therapy, while Atara continues a deep restructuring marked by a roughly 90% headcount reduction in 2025, amended commercialization milestones, a significant lease downsizing, and year-end 2025 cash, cash equivalents and short-term investments of about $8.5 million, subject to audit.
The most recent analyst rating on (ATRA) stock is a Hold with a $18.00 price target. To see the full list of analyst forecasts on Atara Biotherapeutics stock, see the ATRA Stock Forecast page.
On December 30, 2025, Atara Biotherapeutics amended its commercialization agreement with Pierre Fabre Medicament, reducing potential regulatory milestone payments tied to FDA approval of a BLA for tab-cel from $40 million to $31 million in exchange for the opportunity to earn an additional $15 million milestone based on achieving a specified commercial milestone. The revised structure adjusts the balance between regulatory and commercial incentives, potentially aligning Pierre Fabre’s financial commitments more closely with tab-cel’s market performance and affecting the timing and composition of future milestone revenues for Atara.
The most recent analyst rating on (ATRA) stock is a Buy with a $25.00 price target. To see the full list of analyst forecasts on Atara Biotherapeutics stock, see the ATRA Stock Forecast page.