Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 232.84M | 3.55M | 151.00K | 0.00 | 20.10M | 0.00 |
Gross Profit | 231.83M | 3.55M | -664.00K | -1.61M | 19.20M | -605.00K |
EBITDA | 25.08M | -185.82M | -152.18M | -103.06M | -56.37M | -44.92M |
Net Income | 18.77M | -187.35M | -152.99M | -104.68M | -58.74M | -45.36M |
Balance Sheet | ||||||
Total Assets | 757.16M | 615.89M | 370.02M | 306.78M | 255.25M | 269.44M |
Cash, Cash Equivalents and Short-Term Investments | 690.22M | 559.93M | 331.15M | 279.05M | 230.04M | 265.88M |
Total Debt | 17.95M | 18.86M | 14.44M | 13.27M | 1.09M | 899.00K |
Total Liabilities | 50.43M | 44.33M | 37.81M | 29.36M | 12.08M | 7.72M |
Stockholders Equity | 706.73M | 571.55M | 332.21M | 277.42M | 243.17M | 261.72M |
Cash Flow | ||||||
Free Cash Flow | 53.08M | -162.80M | -126.97M | -71.30M | -63.17M | -37.19M |
Operating Cash Flow | 55.04M | -160.87M | -124.51M | -70.06M | -62.15M | -36.89M |
Investing Cash Flow | -1.96M | -1.93M | -2.46M | -1.24M | -1.02M | -294.00K |
Financing Cash Flow | 231.51M | 391.82M | 178.96M | 120.31M | 28.55M | 296.04M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
66 Neutral | $605.58M | 49.54 | 3.33% | ― | 85820.30% | ― | |
66 Neutral | $694.99M | 59.00 | 6.23% | ― | 24.49% | ― | |
54 Neutral | ― | ― | -27.59% | 34.00% | |||
51 Neutral | $7.83B | -0.18 | -40.10% | 2.29% | 21.46% | -2.03% | |
41 Neutral | $603.36M | ― | -379.53% | ― | 366.84% | -35.87% | |
41 Neutral | $673.68M | ― | -31.21% | ― | ― | -5.63% | |
40 Neutral | $760.12M | ― | -59.11% | ― | ― | 39.66% |
On August 20, 2025, Keros Therapeutics announced that the U.S. FDA granted Orphan Drug designation to KER-065 for treating Duchenne muscular dystrophy (DMD). This designation highlights the unmet medical need for DMD patients and marks a significant milestone for Keros as they advance KER-065 into a Phase 2 clinical trial. The Orphan Drug status offers potential benefits like tax credits and market exclusivity, which could enhance Keros’ market positioning and operational strategy in developing treatments for rare diseases.
On August 6, 2025, Keros Therapeutics announced a strategic realignment to focus on the development of its key clinical program, KER-065, while discontinuing the development of cibotercept. This decision follows the analysis of safety and efficacy data from the TROPOS Phase 2 clinical trial in pulmonary arterial hypertension. The company also announced several leadership changes, including the promotion of Lorena Lerner to Chief Scientific Officer and the appointment of Jean-Jacques Bienaimé as Chair of the Board. These changes aim to streamline operations and support Keros’ focus on advancing KER-065, which has shown promising results in a Phase 1 clinical trial and is expected to enter Phase 2 trials for Duchenne muscular dystrophy in early 2026.
On July 17, 2025, Keros Therapeutics announced the dosing of the first patient in the Phase 3 RENEW clinical trial of elritercept for adults with transfusion-dependent anemia and myelodysplastic syndromes. This milestone activates a $10 million payment from Takeda Pharmaceuticals under their global license agreement, highlighting Keros’ progress in developing elritercept as a potentially differentiated therapy for MDS patients. The trial aims to evaluate elritercept’s efficacy in reducing red blood cell transfusions, with Keros eligible for further milestone payments and royalties, potentially exceeding $1.1 billion.
On July 9, 2025, Keros Therapeutics announced the resignation of their Chief Medical Officer, Dr. Yung H. Chyung, effective August 1, 2025. Dr. Chyung’s departure is voluntary and not due to any disagreement with the company. Keros has begun the search for a new Chief Medical Officer, acknowledging Dr. Chyung’s contributions to the company.
On June 4, 2025, Keros Therapeutics held its Annual Meeting of Stockholders, where stockholders voted on three proposals, including the election of directors, ratification of Deloitte & Touche LLP as the independent auditor, and approval of executive compensation. Subsequently, on June 9, 2025, Keros announced the conclusion of its strategic alternatives review, deciding to return $375 million in excess capital to stockholders. This decision reflects a thorough review of capital requirements and stockholder feedback, while the company continues to focus on developing KER-065 for neuromuscular diseases.
On June 6, 2025, Keros Therapeutics announced that its Chair and CEO, Jasbir Seehra, will participate in a fireside chat at the Goldman Sachs 46th Annual Global Healthcare Conference on June 9, 2025. This participation highlights Keros’ engagement with the healthcare investment community and may impact its visibility and industry positioning.
On May 28, 2025, Keros Therapeutics‘ Board of Directors approved a plan to reduce the company’s workforce by approximately 45%, aiming to align operations with strategic priorities and achieve cost savings. This reorganization, expected to be completed by the fourth quarter of 2025, follows the discontinuation of cibotercept development in pulmonary arterial hypertension due to safety concerns observed in the TROPOS trial. The company is evaluating strategic alternatives, including potential business transactions, to maximize shareholder value.