| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 199.19M | 180.27M | 156.37M | 162.05M | 130.86M | 91.92M |
| Gross Profit | 109.92M | 99.52M | 86.40M | 87.09M | 67.38M | 50.76M |
| EBITDA | -5.87M | -10.02M | -26.34M | -33.52M | -45.99M | -51.37M |
| Net Income | -15.96M | -20.92M | -37.49M | -42.78M | -54.37M | -59.86M |
Balance Sheet | ||||||
| Total Assets | 215.19M | 200.92M | 197.75M | 218.09M | 237.50M | 221.41M |
| Cash, Cash Equivalents and Short-Term Investments | 78.51M | 80.45M | 65.85M | 102.15M | 129.36M | 133.59M |
| Total Debt | 98.19M | 98.10M | 96.00M | 87.24M | 87.59M | 66.89M |
| Total Liabilities | 152.98M | 144.02M | 144.30M | 149.53M | 151.88M | 117.61M |
| Stockholders Equity | 61.46M | 56.15M | 52.65M | 67.61M | 84.62M | 103.81M |
Cash Flow | ||||||
| Free Cash Flow | 168.00K | 8.52M | -47.77M | -27.61M | -34.83M | -43.43M |
| Operating Cash Flow | 3.57M | 11.36M | -43.17M | -25.61M | -33.92M | -41.81M |
| Investing Cash Flow | -12.07M | -8.13M | 8.62M | 8.46M | 12.69M | -49.56M |
| Financing Cash Flow | 2.01M | 4.96M | 10.67M | 4.19M | 34.29M | 91.78M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
77 Outperform | $313.08M | 52.43 | 11.05% | ― | 27.37% | 269.84% | |
76 Outperform | $262.70M | 20.90 | 10.53% | ― | 18.90% | 29.22% | |
75 Outperform | $574.25M | 33.19 | 8.80% | ― | 9.28% | 21.00% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
48 Neutral | $338.07M | ― | -27.77% | ― | 13.03% | 21.28% | |
45 Neutral | $229.83M | ― | -42.72% | ― | 4.49% | 3.61% | |
42 Neutral | $82.68M | ― | -92.33% | ― | 4.65% | 68.71% |
Cerus Corporation’s recent earnings call for the third quarter of 2025 painted a picture of robust growth and optimism despite some challenges. The company reported significant revenue growth, driven by strong demand for its INTERCEPT products and successful international expansion efforts. While there are hurdles such as gross margin pressures and regulatory delays in Europe, the overall sentiment remains positive, with raised revenue guidance and a continued focus on operational execution.
Cerus Corporation, a leader in blood safety technology, focuses on developing pathogen-protected blood components to ensure a safe global blood supply. In its latest earnings report, Cerus Corporation announced a record-breaking third quarter for 2025, with total revenue increasing by 19% to $60.2 million and product revenue reaching $52.7 million, marking a 15% year-over-year growth. The company also raised its full-year 2025 product revenue guidance to a range of $202 million to $204 million. Key drivers of this growth include increased demand for the INTERCEPT Blood System and the INTERCEPT Fibrinogen Complex (IFC) in the U.S., with IFC sales up by 110% compared to the previous year. Cerus also completed enrollment in the U.S. RedeS trial, a pivotal Phase 3 clinical trial for its INTERCEPT Blood System for Red Blood Cells, with results expected in 2026. Financially, Cerus reported a near breakeven GAAP net loss of $0.02 million for the third quarter and a positive non-GAAP adjusted EBITDA of $5.0 million. The company remains optimistic about achieving positive full-year 2025 non-GAAP adjusted EBITDA and continues to focus on expanding its market presence and product offerings.
The study titled Comparative Effectiveness of Pathogen Reduced Cryoprecipitated Fibrinogen Complex (INTERCEPT Fibrinogen Complex, IFC) and Cryoprecipitate-AHF (Cryo-AHF) for Treatment of Trauma Associated Hemorrhage: CRYO-FIRST, A Quality Improvement Study aims to assess the feasibility and effectiveness of early administration of IFC in patients with hemorrhagic shock and functional hypofibrinogenemia. This study seeks to determine if advancements in rapid testing and a shelf-stable fibrinogen complex can improve the speed and effectiveness of fibrinogen replacement in trauma care.
Study Overview: Cerus Corporation is conducting a study titled Kinetics of Pathogen Reduced Red Blood Cell Clearance in Subjects Undergoing Red Cell Exchange for Sickle Cell Disease. The study aims to evaluate the recovery and survival of pathogen-reduced red blood cells (RBCs) in patients with sickle cell disease (SCD) undergoing red cell exchange therapy. This research is significant as it could enhance the understanding of RBC clearance kinetics, potentially improving treatment outcomes for SCD patients.
Study Overview: Cerus Corporation is conducting an open-label, controlled Phase 2 study titled Challenge Transfusion of INTERCEPT Pathogen Reduced Red Blood Cells (RBCs) in Subjects With or Without Pre-existing Antibodies to INTERCEPT RBCs. The study aims to assess whether transfusing INTERCEPT RBCs into patients with pre-existing antibodies will increase antibody titers, indicating a secondary immune response, and whether these responses are linked to adverse events, increased RBC clearance, or hemolysis. The study also seeks to evaluate the recovery and survival of INTERCEPT RBCs in patients with various diseases.