ARVN
ARVN
Arvinas, Inc.Income Statement
| Period | Revenue | Operating Expense | Net Income | Net Profit Margin | Earnings Per Share | EBITDA |
|---|---|---|---|---|---|---|
| Q4-2025 | $9.5M ▼ | $80M ▼ | $-67.4M ▼ | -709.47% ▼ | $-1.04 ▼ | $-66M ▼ |
| Q3-2025 | $41.9M ▲ | $85.7M ▼ | $-35.1M ▲ | -83.77% ▲ | $-0.48 ▲ | $-34M ▲ |
| Q2-2025 | $22.4M ▼ | $93.9M ▼ | $-61.2M ▼ | -273.21% ▼ | $-0.84 ▼ | $-70.1M ▼ |
| Q1-2025 | $188.8M ▲ | $117.4M | $82.9M ▲ | 43.91% ▲ | $1.14 ▲ | $72.7M ▲ |
| Q4-2024 | $59.2M | $117.4M | $-45.1M | -76.18% | $-0.63 | $-56.6M |
Balance Statement
| Period | Cash & Short-term | Total Assets | Total Liabilities | Total Equity |
|---|---|---|---|---|
| Q4-2025 | $685.4M ▼ | $717.9M ▼ | $284M ▲ | $433.9M ▼ |
| Q3-2025 | $787.6M ▼ | $844.3M ▼ | $279.9M ▼ | $564.4M ▼ |
| Q2-2025 | $861.2M ▼ | $909.3M ▼ | $300M ▼ | $609.3M ▼ |
| Q1-2025 | $954.3M ▼ | $1B ▼ | $341M ▼ | $660.1M ▲ |
| Q4-2024 | $1.04B | $1.09B | $529.7M | $561.7M |
Cash Flow Statement
| Period | Net Income | Cash From Operations | Cash From Investing | Cash From Financing | Net Change | Free Cash Flow |
|---|---|---|---|---|---|---|
| Q4-2025 | $-67.4M ▼ | $-30.4M ▲ | $145.8M ▲ | $-74M ▼ | $41.4M ▲ | $-30.6M ▲ |
| Q3-2025 | $-35.1M ▲ | $-59.1M ▲ | $63.5M ▼ | $-17.8M ▼ | $-13.4M ▼ | $-59.2M ▲ |
| Q2-2025 | $-61.2M ▼ | $-95.4M ▼ | $128.8M ▲ | $500K ▲ | $33.9M ▲ | $-96.6M ▼ |
| Q1-2025 | $82.9M ▲ | $-88.9M ▼ | $69.5M ▼ | $-100K ▼ | $-19.5M ▼ | $-89.3M ▼ |
| Q4-2024 | $-45.1M | $-84.1M | $98.9M | $500K | $15.3M | $-84.4M |
Revenue by Products
| Product | Q1-2025 | Q2-2025 | Q3-2025 | Q4-2025 |
|---|---|---|---|---|
License | $130.00M ▲ | $130.00M ▲ | $130.00M ▲ | $0 ▼ |
Q4 2025 Earnings Call Summary
Read Call Summary5-Year Trend Analysis
A comprehensive look at Arvinas, Inc.'s financial evolution and strategic trajectory over the past five years.
Arvinas combines a strong scientific position in a cutting-edge drug modality with a comparatively conservative financial structure. It has substantial cash and investments, minimal debt, and partnerships with top-tier pharma companies that validate its technology and may provide future milestone and royalty streams. The PROTAC platform, growing clinical pipeline across oncology and neurology, and demonstrated ability to generate orally available and brain-penetrant degraders together form a compelling foundation. Operationally, the company has taken steps to prioritize its most differentiated programs, signaling an awareness of capital discipline even while investing heavily in R&D.
Key risks center on continued losses, significant cash burn, and the inherently binary nature of clinical and regulatory outcomes. The company’s negative profitability and free cash flow mean that, absent major commercial success or very large partnership inflows, additional capital raises are a realistic possibility over time, with potential dilution for existing shareholders. Scientifically, failure or delay of lead programs—especially vepdegestrant or key oncology and neurology assets—could materially alter the company’s trajectory. Competitive pressure in protein degradation and in the broader oncology and neurology landscapes is increasing, and dependence on partners introduces another layer of strategic and execution risk.
Looking forward, Arvinas appears to be approaching a critical transition period. Over the next several years, pivotal regulatory decisions, first commercial launches (if approvals are granted), and maturing early-stage programs will likely determine whether the company can evolve from a cash-burning R&D platform into a sustainable commercial enterprise. Its strong liquidity and low leverage provide time and flexibility, while its scientific platform and partnerships offer meaningful upside if the data continue to support its approach. At the same time, uncertainty remains high, as is typical for clinical-stage biotech: the company’s long-term outlook will ultimately be shaped by the success of a few flagship programs and the broader market’s adoption of targeted protein degradation as a mainstream therapeutic modality.
About Arvinas, Inc.
https://www.arvinas.comArvinas, Inc., a clinical-stage biopharmaceutical company, engages in the discovery, development, and commercialization of therapies to degrade disease-causing proteins.
Income Statement
| Period | Revenue | Operating Expense | Net Income | Net Profit Margin | Earnings Per Share | EBITDA |
|---|---|---|---|---|---|---|
| Q4-2025 | $9.5M ▼ | $80M ▼ | $-67.4M ▼ | -709.47% ▼ | $-1.04 ▼ | $-66M ▼ |
| Q3-2025 | $41.9M ▲ | $85.7M ▼ | $-35.1M ▲ | -83.77% ▲ | $-0.48 ▲ | $-34M ▲ |
| Q2-2025 | $22.4M ▼ | $93.9M ▼ | $-61.2M ▼ | -273.21% ▼ | $-0.84 ▼ | $-70.1M ▼ |
| Q1-2025 | $188.8M ▲ | $117.4M | $82.9M ▲ | 43.91% ▲ | $1.14 ▲ | $72.7M ▲ |
| Q4-2024 | $59.2M | $117.4M | $-45.1M | -76.18% | $-0.63 | $-56.6M |
Balance Statement
| Period | Cash & Short-term | Total Assets | Total Liabilities | Total Equity |
|---|---|---|---|---|
| Q4-2025 | $685.4M ▼ | $717.9M ▼ | $284M ▲ | $433.9M ▼ |
| Q3-2025 | $787.6M ▼ | $844.3M ▼ | $279.9M ▼ | $564.4M ▼ |
| Q2-2025 | $861.2M ▼ | $909.3M ▼ | $300M ▼ | $609.3M ▼ |
| Q1-2025 | $954.3M ▼ | $1B ▼ | $341M ▼ | $660.1M ▲ |
| Q4-2024 | $1.04B | $1.09B | $529.7M | $561.7M |
Cash Flow Statement
| Period | Net Income | Cash From Operations | Cash From Investing | Cash From Financing | Net Change | Free Cash Flow |
|---|---|---|---|---|---|---|
| Q4-2025 | $-67.4M ▼ | $-30.4M ▲ | $145.8M ▲ | $-74M ▼ | $41.4M ▲ | $-30.6M ▲ |
| Q3-2025 | $-35.1M ▲ | $-59.1M ▲ | $63.5M ▼ | $-17.8M ▼ | $-13.4M ▼ | $-59.2M ▲ |
| Q2-2025 | $-61.2M ▼ | $-95.4M ▼ | $128.8M ▲ | $500K ▲ | $33.9M ▲ | $-96.6M ▼ |
| Q1-2025 | $82.9M ▲ | $-88.9M ▼ | $69.5M ▼ | $-100K ▼ | $-19.5M ▼ | $-89.3M ▼ |
| Q4-2024 | $-45.1M | $-84.1M | $98.9M | $500K | $15.3M | $-84.4M |
Revenue by Products
| Product | Q1-2025 | Q2-2025 | Q3-2025 | Q4-2025 |
|---|---|---|---|---|
License | $130.00M ▲ | $130.00M ▲ | $130.00M ▲ | $0 ▼ |
Q4 2025 Earnings Call Summary
Read Call Summary5-Year Trend Analysis
A comprehensive look at Arvinas, Inc.'s financial evolution and strategic trajectory over the past five years.
Arvinas combines a strong scientific position in a cutting-edge drug modality with a comparatively conservative financial structure. It has substantial cash and investments, minimal debt, and partnerships with top-tier pharma companies that validate its technology and may provide future milestone and royalty streams. The PROTAC platform, growing clinical pipeline across oncology and neurology, and demonstrated ability to generate orally available and brain-penetrant degraders together form a compelling foundation. Operationally, the company has taken steps to prioritize its most differentiated programs, signaling an awareness of capital discipline even while investing heavily in R&D.
Key risks center on continued losses, significant cash burn, and the inherently binary nature of clinical and regulatory outcomes. The company’s negative profitability and free cash flow mean that, absent major commercial success or very large partnership inflows, additional capital raises are a realistic possibility over time, with potential dilution for existing shareholders. Scientifically, failure or delay of lead programs—especially vepdegestrant or key oncology and neurology assets—could materially alter the company’s trajectory. Competitive pressure in protein degradation and in the broader oncology and neurology landscapes is increasing, and dependence on partners introduces another layer of strategic and execution risk.
Looking forward, Arvinas appears to be approaching a critical transition period. Over the next several years, pivotal regulatory decisions, first commercial launches (if approvals are granted), and maturing early-stage programs will likely determine whether the company can evolve from a cash-burning R&D platform into a sustainable commercial enterprise. Its strong liquidity and low leverage provide time and flexibility, while its scientific platform and partnerships offer meaningful upside if the data continue to support its approach. At the same time, uncertainty remains high, as is typical for clinical-stage biotech: the company’s long-term outlook will ultimately be shaped by the success of a few flagship programs and the broader market’s adoption of targeted protein degradation as a mainstream therapeutic modality.

CEO
John G. Houston
Compensation Summary
(Year 2024)
Upcoming Earnings
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Ratings Snapshot
Rating : C
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