| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 312.30M | 263.40M | 78.50M | 131.40M | 53.60M | 25.90M |
| Gross Profit | 312.30M | 263.40M | 78.50M | 131.40M | 53.60M | 25.90M |
| EBITDA | -88.00M | -243.60M | -394.80M | -255.00M | -182.40M | -117.60M |
| Net Income | -58.50M | -198.90M | -367.30M | -282.50M | -191.00M | -119.30M |
Balance Sheet | ||||||
| Total Assets | 844.30M | 1.09B | 1.30B | 1.27B | 1.58B | 717.40M |
| Cash, Cash Equivalents and Short-Term Investments | 787.60M | 1.04B | 1.26B | 1.21B | 1.50B | 688.60M |
| Total Debt | 9.50M | 9.70M | 3.20M | 5.50M | 5.00M | 4.10M |
| Total Liabilities | 279.90M | 529.70M | 644.60M | 703.90M | 799.90M | 75.20M |
| Stockholders Equity | 564.40M | 561.70M | 660.00M | 564.90M | 781.70M | 642.20M |
Cash Flow | ||||||
| Free Cash Flow | -329.50M | -261.10M | -350.70M | -280.30M | 554.70M | -96.20M |
| Operating Cash Flow | -327.50M | -259.30M | -347.80M | -273.50M | 559.40M | -89.76M |
| Investing Cash Flow | 360.70M | 34.70M | 203.50M | 242.80M | -1.31B | 164.25M |
| Financing Cash Flow | -16.90M | 7.90M | 374.70M | 4.70M | 278.60M | 504.67M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
61 Neutral | $750.14M | -14.54 | ― | ― | ― | ― | |
60 Neutral | $887.53M | -10.90 | -37.82% | ― | -100.00% | -28.79% | |
54 Neutral | $646.34M | -3.80 | -611.42% | ― | 96.83% | -61.92% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
49 Neutral | $1.36B | -17.41 | -308.02% | ― | 196.42% | 53.92% | |
48 Neutral | $964.16M | -7.89 | -26.64% | ― | ― | -103.95% | |
46 Neutral | $2.20B | -15.41 | -59.22% | ― | ― | 17.23% |
On December 6, 2025, Arvinas, Inc. announced preclinical data for ARV-393, a PROTAC BCL6 degrader, in combination with glofitamab, a CD20×CD3 bispecific antibody, at the 67th American Society of Hematology Annual Meeting. The data demonstrated that the combination significantly enhanced tumor growth inhibition and increased tumor regression rates in a high-grade B-cell lymphoma model compared to either agent alone. These findings suggest mechanistic synergies between ARV-393 and T-cell engagement, supporting the initiation of a Phase 1 clinical trial in 2026 to explore this combination as a chemotherapy-free treatment for diffuse large B-cell lymphoma.
On October 24, 2025, Arvinas, Inc. announced preclinical data for ARV-806, a PROTAC KRAS G12D degrader, at the 2025 AACR-NCI-EORTC International Conference. The data showed ARV-806’s potential as a best-in-class therapy for KRAS G12D mutated cancers, demonstrating significant potency in degrading KRAS G12D protein and reducing cancer cell proliferation across pancreatic, colorectal, and lung cancer models. The company is currently evaluating ARV-806 in a Phase 1 clinical trial for patients with advanced solid tumors harboring KRAS G12D mutations, highlighting its potential to address high unmet needs in these cancers.
On October 20, 2025, Arvinas announced new patient-reported outcomes from its Phase 3 VERITAC-2 clinical trial for vepdegestrant, presented at the ESMO 2025 Congress. Vepdegestrant, developed with Pfizer, showed significant improvements in quality of life and delayed deterioration in patients with ESR1-mutated, ER+/HER2- advanced breast cancer compared to fulvestrant. The trial results reinforce vepdegestrant’s potential as a promising treatment option, highlighting its clinical benefits and supporting its development as a monotherapy for this patient group.
On October 5, 2025, Arvinas, Inc. announced positive Phase 1 clinical trial results for ARV-102, a PROTAC LRRK2 degrader, presented at the 2025 International Congress of Parkinson’s Disease and Movement Disorders. The trials, conducted on healthy volunteers and Parkinson’s disease patients, demonstrated that ARV-102 was well tolerated and showed dose-dependent increases in cerebrospinal fluid exposure, indicating brain penetration. Significant reductions in LRRK2 protein and pathway biomarkers were observed, supporting further development of ARV-102 for Parkinson’s disease and progressive supranuclear palsy. The company plans to present additional data in 2026 and initiate a Phase 1b trial for progressive supranuclear palsy.
On September 17, 2025, Arvinas announced a 15% workforce reduction primarily affecting roles related to the commercialization of vepdegestrant, expecting to incur $4.5 million in related costs. The company also updated its collaboration with Pfizer, agreeing to out-license vepdegestrant’s commercialization rights to a third party, aiming to optimize costs and streamline operations. Additionally, Arvinas introduced a $100 million share repurchase program, reflecting confidence in its business strength and commitment to maximizing shareholder value. These strategic actions are expected to save over $100 million annually compared to FY 2024 and extend the company’s cash runway into the second half of 2028.