| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 192.51M | 180.27M | 156.37M | 162.05M | 130.86M | 91.92M |
| Gross Profit | 107.98M | 99.52M | 86.40M | 87.09M | 67.38M | 50.76M |
| EBITDA | -8.62M | -9.88M | -26.54M | -34.08M | -45.99M | -51.37M |
| Net Income | -18.88M | -20.92M | -37.49M | -42.83M | -54.38M | -59.86M |
Balance Sheet | ||||||
| Total Assets | 213.07M | 200.92M | 197.75M | 218.09M | 237.50M | 221.41M |
| Cash, Cash Equivalents and Short-Term Investments | 78.03M | 80.45M | 65.85M | 102.15M | 129.36M | 133.59M |
| Total Debt | 98.90M | 98.10M | 96.00M | 87.24M | 87.59M | 66.89M |
| Total Liabilities | 156.90M | 144.02M | 144.30M | 149.53M | 151.88M | 117.61M |
| Stockholders Equity | 55.43M | 56.15M | 52.65M | 67.61M | 84.62M | 103.81M |
Cash Flow | ||||||
| Free Cash Flow | 3.42M | 8.52M | -47.77M | -27.61M | -34.83M | -42.36M |
| Operating Cash Flow | 5.71M | 11.36M | -43.17M | -25.61M | -33.92M | -40.74M |
| Investing Cash Flow | -4.75M | -8.13M | 8.62M | 8.46M | 12.69M | -49.56M |
| Financing Cash Flow | 1.75M | 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 |
|---|---|---|---|---|---|---|---|
76 Outperform | $320.99M | 57.58 | 9.70% | ― | 27.22% | 695.07% | |
71 Outperform | $253.66M | 19.30 | 10.79% | ― | 17.11% | 45.34% | |
70 Outperform | $495.40M | 28.63 | 8.80% | ― | 6.15% | -54.24% | |
63 Neutral | $279.66M | ― | -46.85% | ― | 14.65% | -86.36% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | $277.96M | ― | -35.98% | ― | 13.25% | 23.81% | |
50 Neutral | $226.61M | ― | -87.65% | ― | 2.47% | 56.93% |
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.
Cerus Corporation’s recent earnings call for Q2 2025 paints a picture of robust growth and strategic advancements, coupled with some regional challenges. The company reported significant increases in product revenue and successful regulatory progress, signaling a strong business trajectory. However, it also faces potential hurdles in China and Germany, which could impact future operations.
Cerus Corporation is a company focused on enhancing blood safety and availability globally, primarily through its INTERCEPT Blood System, which is the only pathogen reduction system with both CE mark and FDA approval for platelets and plasma. The company is headquartered in Concord, California, and is dedicated to safeguarding the world’s blood supply.