| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 16.86M | 74.20M | 86.18M | 1.62B | 1.10B | 67.25M |
| Gross Profit | -438.52M | -404.44M | -486.65M | 994.83M | 581.54M | 67.25M |
| EBITDA | -511.54M | -508.91M | -641.64M | 839.85M | 426.56M | -291.54M |
| Net Income | -499.65M | -521.96M | -615.06M | 515.84M | 528.58M | -298.67M |
Balance Sheet | ||||||
| Total Assets | 1.02B | 1.40B | 1.92B | 2.80B | 1.95B | 918.76M |
| Cash, Cash Equivalents and Short-Term Investments | 506.51M | 905.35M | 1.52B | 2.40B | 708.14M | 736.86M |
| Total Debt | 100.17M | 97.89M | 124.54M | 127.97M | 137.49M | 70.18M |
| Total Liabilities | 223.35M | 248.43M | 328.82M | 724.13M | 522.42M | 201.91M |
| Stockholders Equity | 796.10M | 1.15B | 1.59B | 2.08B | 1.43B | 716.85M |
Cash Flow | ||||||
| Free Cash Flow | -460.43M | -453.65M | -800.36M | 1.60B | -69.41M | -197.49M |
| Operating Cash Flow | -453.54M | -446.35M | -778.78M | 1.66B | -47.59M | -190.94M |
| Investing Cash Flow | 364.46M | 499.37M | 164.73M | -1.19B | -140.81M | -9.86M |
| Financing Cash Flow | 4.01M | 4.39M | 7.38M | 34.76M | 100.33M | 529.47M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
62 Neutral | $435.13M | -9.03 | -43.11% | ― | ― | -5.71% | |
55 Neutral | $1.05B | -2.15 | -49.06% | ― | -78.55% | 7.74% | |
54 Neutral | $1.06B | -15.76 | -22.38% | ― | 2147.20% | -269.99% | |
52 Neutral | $1.09B | ― | -53.89% | ― | 175.62% | 19.63% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
47 Neutral | $1.30B | -1.55 | ― | ― | -12.52% | -82.84% | |
46 Neutral | $881.92M | -6.97 | -19.61% | ― | 38.16% | 48.43% |
On January 12, 2026, Vir Biotechnology reported updated positive Phase 2 SOLSTICE data in chronic hepatitis delta showing that combination therapy with tobevibart and elebsiran achieved undetectable HDV RNA in 88% of evaluable participants at Week 96, with a favorable safety profile and stronger viral suppression than tobevibart alone, reinforcing the potential of this regimen as a future standard of care. The company outlined progress in its registrational ECLIPSE Phase 3 program in chronic hepatitis delta, highlighted upcoming presentations of Phase 1 data for PSMA-targeted T-cell engager VIR-5500 in metastatic castration-resistant prostate cancer at a major oncology meeting, and noted continued advancement of its broader PRO-XTEN oncology portfolio, while disclosing an unaudited year-end 2025 cash and investment balance of about $781 million and an extended cash runway into the fourth quarter of 2027, supported by a regional licensing deal with Norgine and disciplined spending.
The most recent analyst rating on (VIR) stock is a Buy with a $13.00 price target. To see the full list of analyst forecasts on Vir Biotechnology stock, see the VIR Stock Forecast page.
On December 16, 2025, Vir Biotechnology entered into a license agreement with Norgine Pharma UK Limited, granting Norgine exclusive commercial rights to a combination treatment for chronic hepatitis delta (CHD) in Europe, Australia, and New Zealand. Vir will receive an initial EUR 55 million reimbursement and up to EUR 495 million in milestones, with shared clinical development costs for ongoing trials. The combination treatment of tobevibart and elebsiran showed promising results in a Phase 2 trial, achieving significant virologic suppression and being well-tolerated, which could enhance Vir’s market positioning and impact stakeholders positively.
The most recent analyst rating on (VIR) stock is a Buy with a $15.00 price target. To see the full list of analyst forecasts on Vir Biotechnology stock, see the VIR Stock Forecast page.