| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 596.57M | 3.55M | 240.74M | 243.23M | 138.29M | 87.99M |
| Gross Profit | 576.77M | 3.55M | 240.74M | 243.23M | 138.29M | 87.99M |
| EBITDA | -52.51M | -561.51M | -175.67M | -162.29M | -132.58M | -87.22M |
| Net Income | -148.42M | -599.49M | -205.28M | -176.06M | -140.85M | -84.55M |
Balance Sheet | ||||||
| Total Assets | 1.38B | 1.14B | 765.55M | 691.94M | 710.15M | 522.50M |
| Cash, Cash Equivalents and Short-Term Investments | 900.37M | 680.96M | 403.63M | 376.40M | 367.79M | 315.49M |
| Total Debt | 713.29M | 510.55M | 383.50M | 81.58M | 25.55M | 21.14M |
| Total Liabilities | 860.81M | 948.74M | 478.39M | 273.60M | 301.33M | 60.72M |
| Stockholders Equity | 519.81M | 185.44M | 271.34M | 398.52M | 408.82M | 461.78M |
Cash Flow | ||||||
| Free Cash Flow | -17.62M | -604.32M | -330.63M | -188.91M | 147.66M | -107.34M |
| Operating Cash Flow | 21.84M | -462.85M | -153.89M | -136.13M | 171.22M | -95.39M |
| Investing Cash Flow | -424.84M | -420.07M | -96.16M | -5.42M | -141.68M | -240.78M |
| Financing Cash Flow | 459.43M | 870.52M | 253.05M | 65.19M | 11.30M | 257.95M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
80 Outperform | $5.92B | 30.61 | 19.66% | ― | 54.51% | 275.94% | |
74 Outperform | $4.74B | 14.19 | 22.35% | ― | 1.08% | 3.40% | |
73 Outperform | $3.91B | 14.86 | 34.95% | ― | 12.69% | 100.80% | |
57 Neutral | $5.23B | -29.96 | -34.80% | ― | 2816.21% | 73.33% | |
52 Neutral | $5.18B | ― | -47.18% | ― | -76.96% | -425.41% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $6.36B | ― | -20.83% | ― | ― | -5.21% |
Arrowhead Pharmaceuticals, Inc. has launched a new clinical study titled ‘A Phase 1/2a Placebo-Controlled Dose-Escalating Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ARO-MAPT-SC in Healthy Subjects and Subjects With Early Alzheimer’s Disease.’ The study aims to assess the safety and effectiveness of ARO-MAPT-SC, a potential treatment for early Alzheimer’s disease, in both healthy individuals and those with mild cognitive impairment or mild dementia due to Alzheimer’s.
Arrowhead Pharmaceuticals, Inc. is conducting a Phase 3 clinical study titled ‘YOSEMITE’ to evaluate the efficacy and safety of Zodasiran in treating Homozygous Familial Hypercholesterolemia (HoFH) in adolescents and adults. This condition is characterized by extremely high cholesterol levels, and the study aims to provide a new treatment option for affected individuals.
Arrowhead Pharmaceuticals, Inc. is conducting a clinical study titled ‘A Phase1/2a Dose-Escalating Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ARO-DUX4 in Adult Patients and Adolescent Patients With Facioscapulohumeral Muscular Dystrophy Type 1.’ The study aims to assess the safety and effectiveness of ARO-DUX4, a potential treatment for Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1), a genetic muscle disorder. This research is significant as it could lead to new therapeutic options for FSHD1 patients.
Arrowhead Pharmaceuticals, Inc. is conducting a Phase 3 open-label extension study titled ‘A Phase 3 Open-Label Extension Study to Evaluate the Long-Term Safety and Efficacy of Plozasiran in Adults With Hypertriglyceridemia (SHASTA-10 Study).’ The study aims to assess the long-term safety and efficacy of Plozasiran in adults with hypertriglyceridemia, a condition characterized by elevated triglyceride levels, which can lead to cardiovascular issues. This study is significant as it could provide a new therapeutic option for managing hypertriglyceridemia.
Arrowhead Pharmaceuticals, Inc. is conducting a Phase 1 clinical study titled A Phase 1 Placebo-Controlled Dose Escalating Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ARO-ATXN2 in Adult Subjects With Spinocerebellar Ataxia Type 2. The study aims to assess the safety and effectiveness of ARO-ATXN2 in adults with Spinocerebellar Ataxia Type 2 (SCA2), a genetic disorder characterized by progressive problems with movement.
Arrowhead Pharmaceuticals, Inc. is conducting a clinical study titled A Phase 1/2a Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ARO-INHBE in Adult Volunteers With Obesity With and Without Diabetes Mellitus. The study aims to assess the safety and effectiveness of ARO-INHBE, a potential treatment for obesity, with a focus on its pharmacokinetics and pharmacodynamics in adults, both with and without type 2 diabetes.
Arrowhead Pharmaceuticals, Inc. is conducting a clinical study titled A Phase 1/2A Dose-Escalating Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ARO-ALK7 in Adult Volunteers With Obesity With and Without Type 2 Diabetes Mellitus. The study aims to assess the safety and effectiveness of ARO-ALK7 in adults with obesity, both with and without Type 2 Diabetes Mellitus (T2DM), highlighting its potential significance in addressing obesity-related health issues.
Arrowhead Pharmaceuticals is conducting a Phase 3 clinical study titled ‘Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Plozasiran in Adults With Severe Hypertriglyceridemia at High Risk of Acute Pancreatitis (SHASTA-5 Study).’ The primary objective is to assess the efficacy and safety of plozasiran in reducing the risk of acute pancreatitis in adults with severe hypertriglyceridemia, a condition characterized by extremely high levels of triglycerides in the blood, which can lead to pancreatitis.
Arrowhead Pharmaceuticals, Inc. is conducting a study titled ‘A Phase 1/2a Dose-Escalating Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ARO-DM1 in Subjects With Type 1 Myotonic Dystrophy Who Are ≥18 to ≤ 65 Years.’ The study aims to assess the safety and effectiveness of ARO-DM1, a potential treatment for Type 1 Myotonic Dystrophy, a genetic disorder affecting muscle function.
On September 11, 2025, Ionis Pharmaceuticals filed a patent infringement lawsuit against Arrowhead Pharmaceuticals, alleging that Arrowhead’s planned commercialization of the investigational drug plozasiran infringes on Ionis’s U.S. Patent No. 9,593,333. This legal action follows Arrowhead’s own filing on September 10, 2025, seeking a declaratory judgment that the patent is invalid and not infringed. The outcome of this legal dispute could significantly impact Arrowhead’s operations and its position in the market for treatments targeting familial chylomicronemia syndrome (FCS), as well as its stakeholders.
The most recent analyst rating on (ARWR) stock is a Buy with a $42.00 price target. To see the full list of analyst forecasts on Arrowhead Pharmaceuticals stock, see the ARWR Stock Forecast page.
On September 10, 2025, Arrowhead Pharmaceuticals filed a lawsuit against Ionis Pharmaceuticals in the United States District Court for the District of Delaware. The lawsuit seeks a declaratory judgment that Ionis’s U.S. Patent No. 9,593,333 is invalid and/or not infringed by Arrowhead’s planned commercialization of investigational plozasiran. This legal action could impact Arrowhead’s operations and its position in the RNAi therapeutics market, particularly concerning its advanced drug candidate, plozasiran, which has shown promise in treating familial chylomicronemia syndrome (FCS) by significantly reducing triglycerides and pancreatitis risk in patients.
The most recent analyst rating on (ARWR) stock is a Buy with a $42.00 price target. To see the full list of analyst forecasts on Arrowhead Pharmaceuticals stock, see the ARWR Stock Forecast page.
On September 2, 2025, Arrowhead Pharmaceuticals entered into an exclusive licensing and collaboration agreement with Novartis Pharma AG for ARO-SNCA, a preclinical stage RNA interference therapeutic for Parkinson’s Disease. Arrowhead will receive a $200 million upfront payment and could earn up to $2 billion in milestone payments, with Novartis taking responsibility for clinical development and commercialization. This partnership highlights Arrowhead’s strategic positioning in the CNS space and the potential impact of its TRiMTM platform in advancing treatments for neurodegenerative diseases.
The most recent analyst rating on (ARWR) stock is a Buy with a $80.00 price target. To see the full list of analyst forecasts on Arrowhead Pharmaceuticals stock, see the ARWR Stock Forecast page.
Arrowhead Pharmaceuticals, Inc. is conducting a Phase 3 open-label extension study titled A Phase 3 Open-Label Extension Study to Evaluate the Long-Term Safety and Efficacy of Plozasiran in Adults With Hypertriglyceridemia (SHASTA-10 Study). The study aims to assess the long-term safety and efficacy of Plozasiran in adults with hypertriglyceridemia and severe hypertriglyceridemia, building on previous research to provide more comprehensive data on its effects.
Arrowhead Pharmaceuticals’ recent earnings call highlighted the company’s robust progress across various clinical programs, strategic partnerships, and a solid financial position. Despite facing increased operational costs and external factors affecting its stock price, the overall sentiment was positive, reflecting confidence in the company’s strategic direction and future prospects.
Arrowhead Pharmaceuticals, Inc. is a biotechnology company specializing in the development of RNA interference (RNAi) therapeutics aimed at treating intractable diseases by silencing the genes responsible for them. The company leverages a broad portfolio of RNA chemistries and efficient delivery mechanisms to induce gene knockdown, positioning itself as a leader in the RNAi sector.