| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 240.00M | 258.00M | 117.00M | 112.00M | 383.00M | 78.00M |
| Gross Profit | 238.00M | 258.00M | 117.00M | 112.00M | 383.00M | 78.00M |
| EBITDA | -323.00M | -269.00M | -291.00M | -258.00M | 59.00M | -120.00M |
| Net Income | -349.00M | -283.00M | -307.00M | -267.00M | 53.00M | -123.00M |
Balance Sheet | ||||||
| Total Assets | 974.00M | 1.15B | 1.09B | 1.34B | 1.59B | 772.29M |
| Cash, Cash Equivalents and Short-Term Investments | 831.00M | 978.00M | 759.00M | 1.01B | 499.31M | 728.65M |
| Total Debt | 111.00M | 60.00M | 11.00M | 120.00M | 121.99M | 18.11M |
| Total Liabilities | 538.00M | 665.00M | 633.00M | 688.00M | 750.45M | 269.99M |
| Stockholders Equity | 436.00M | 485.00M | 462.00M | 657.00M | 841.45M | 502.30M |
Cash Flow | ||||||
| Free Cash Flow | -464.00M | -176.00M | -330.00M | 432.00M | -282.25M | 108.11M |
| Operating Cash Flow | -462.00M | -170.00M | -306.00M | 438.00M | -256.17M | 111.17M |
| Investing Cash Flow | 299.00M | -84.00M | 194.00M | -413.00M | -3.87M | -434.37M |
| Financing Cash Flow | 200.00M | 277.00M | 33.00M | 33.00M | 237.34M | 438.68M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
62 Neutral | $350.24M | -7.15 | -43.11% | ― | ― | -5.71% | |
55 Neutral | $2.76B | ― | -68.13% | ― | -8.75% | -8.79% | |
52 Neutral | ― | ― | ― | ― | 271.44% | 26.65% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
43 Neutral | $2.57B | -15.37 | -32.63% | ― | ― | -123.65% | |
42 Neutral | $757.76M | -2.69 | -96.24% | ― | ― | -15.77% | |
33 Underperform | $1.27B | -4.64 | -96.11% | ― | ― | 31.16% |
On December 18, 2025, Arcus Biosciences amended its existing loan and security agreement with a syndicate of lenders led by Hercules Capital, restructuring access to the remaining $150 million term loan facility into four tranches tied to specific time windows and clinical and regulatory milestones, and extending the facility’s maturity date to September 1, 2030. The amendment introduces new performance covenants that apply if outstanding borrowings exceed $200 million, requiring Arcus, after achieving an FDA approval milestone, to maintain either a minimum market capitalization with sufficient qualified cash, higher levels of qualified cash alone, or to meet defined net product revenue thresholds, effectively tightening financial discipline as the company advances its late-stage programs and approaches potential commercialization.
On December 12, 2025, Arcus Biosciences announced the discontinuation of its Phase 3 STAR-221 study due to futility, as the combination of domvanalimab and zimberelimab with chemotherapy did not improve overall survival compared to nivolumab with chemotherapy in treating advanced gastric and esophageal cancers. The company, in collaboration with Gilead Sciences, will focus on analyzing these results and redirecting its R&D efforts towards casdatifan, a potential best-in-class HIF-2a inhibitor, and other emerging programs, with sufficient funding expected to last until at least the second half of 2028.
Arcus Biosciences, Inc. recently completed a public offering of its common stock, selling a total of 15,755,000 shares at $18.25 per share, including the full exercise of the underwriters’ option. The offering, which closed on November 3, 2025, generated approximately $269.7 million in net proceeds for the company, after accounting for underwriting discounts, commissions, and estimated expenses.
On October 12, 2025, Arcus Biosciences announced the first overall survival results from the Phase 2 EDGE-Gastric study, showing promising efficacy of the domvanalimab plus zimberelimab and chemotherapy regimen in patients with advanced gastric and esophageal cancers. The study, which evaluated 41 patients, demonstrated sustained efficacy across all PD-L1 subgroups with a median overall survival of 26.7 months and a favorable safety profile, indicating potential advancements in cancer treatment options.
On October 6, 2025, Arcus Biosciences presented updated data from its ARC-20 Phase 1/1b study, which evaluates the efficacy and safety of casdatifan in patients with metastatic clear cell renal cell carcinoma. The data, as of August 15, 2025, showed promising results in terms of progression-free survival and disease control rates, with no unexpected safety concerns. Additionally, Arcus announced plans to expand into immunology and inflammation, with potential new drug candidates targeting conditions such as atopic dermatitis, rheumatoid arthritis, and multiple sclerosis, aiming to initiate clinical studies in 2026.