| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 14.53M | 74.20M | 86.18M | 1.58B | 1.09B | 67.25M |
| Gross Profit | -83.69M | 73.36M | 83.42M | 1.43B | 1.02B | -234.33M |
| EBITDA | -542.61M | -537.61M | -664.85M | 833.07M | 420.75M | -289.80M |
| 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 | 500.05M | 905.35M | 1.52B | 2.40B | 708.14M | 736.86M |
| Total Debt | 91.22M | 97.89M | 124.54M | 127.97M | 133.56M | 66.56M |
| 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 | -455.95M | -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 | 164.63M | -1.19B | -140.81M | -9.86M |
| Financing Cash Flow | 4.01M | 4.39M | 7.48M | 34.76M | 100.33M | 529.47M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
62 Neutral | $641.63M | ― | -43.63% | ― | ― | -13.05% | |
54 Neutral | $1.02B | -7.88 | -19.61% | ― | 38.16% | 48.43% | |
52 Neutral | $867.63M | ― | -32.78% | ― | -13.37% | -1025.90% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
45 Neutral | $658.57M | ― | -53.16% | ― | 636.99% | 27.10% | |
42 Neutral | $729.31M | ― | -49.06% | ― | -78.55% | 7.74% | |
41 Neutral | $616.04M | -0.99 | ― | ― | -12.52% | -82.84% |
Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on developing transformative therapies for serious infectious diseases and cancer, leveraging its expertise in the immune system and innovative technologies like the PRO-XTEN masking platform.
Study Overview: Vir Biotechnology, Inc. is conducting a Phase 2b study titled ‘A Phase 2b Randomized, Open-Label Study to Evaluate the Efficacy and Safety of Tobevibart+Elebsiran Combination Therapy Versus Bulevirtide in Participants With Chronic HDV Infection (ECLIPSE 3)’. The study aims to assess the efficacy and safety of a new combination therapy for chronic Hepatitis D Virus (HDV) infection, a significant health concern due to its severe liver complications.
Vir Biotechnology, Inc. is conducting a Phase 3 clinical study titled ‘A Phase 3 Randomized, Open-Label Study to Evaluate the Efficacy and Safety of Tobevibart+Elebsiran Combination Therapy in Participants With Chronic HDV Infection Not Virologically Suppressed With Bulevirtide (ECLIPSE 2)’. The study aims to assess the effectiveness and safety of a combination therapy for patients with chronic hepatitis D virus (HDV) infection who have not responded to bulevirtide treatment.
Study Overview: Vir Biotechnology, Inc. is conducting a Phase 3 study titled A Phase 3 Randomized, Open-Label Study to Evaluate the Efficacy and Safety of Tobevibart + Elebsiran Combination Therapy in Participants With Chronic HDV Infection (ECLIPSE 1). The study aims to assess the effectiveness and safety of the combination therapy for treating chronic hepatitis delta, a significant health concern due to its severe liver complications.
Study Overview: Vir Biotechnology, Inc. is conducting a Phase 1 clinical study titled A Phase 1, Multicenter, Open-Label, First-in-Human Study of the Safety and Pharmacokinetics of VIR-5818 Alone and in Combination With Pembrolizumab in Participants With Locally Advanced or Metastatic HER2-Expressing Cancers. The study aims to assess the safety, pharmacokinetics, and preliminary activity of VIR-5818, both alone and combined with pembrolizumab, in treating HER2+ tumors. This research is significant as it explores new treatment avenues for challenging cancer types.
Vir Biotechnology, Inc. is conducting a Phase 1 study titled A Phase 1, First-in-Human Study of the Safety, Pharmacokinetics, and Preliminary Efficacy of VIR-5500 (AMX-500) in Participants With Prostate Cancer. The study aims to evaluate the safety and efficacy of VIR-5500 in treating hormone-refractory prostate cancer, a significant step in addressing this challenging condition.
Study Overview: Vir Biotechnology, Inc. is conducting a Phase 1 clinical study titled ‘A Phase 1, First-in-Human Study of the Safety, Pharmacokinetics, and Preliminary Efficacy of VIR-5525 Alone and in Combination With Pembrolizumab in Participants With Locally Advanced or Metastatic Solid Tumors.’ The study aims to evaluate the safety, pharmacokinetics, and preliminary anti-tumor activity of VIR-5525, both as a standalone treatment and in combination with pembrolizumab, for patients with EGFR-positive solid tumors.
Vir Biotechnology, Inc. is conducting a Phase 1 study titled Effect of Hepatic Impairment on the Pharmacokinetics and Safety of VIR-2218 and VIR-3434. The study aims to evaluate the pharmacokinetics, safety, and tolerability of VIR-2218 and VIR-3434, both as monotherapies and in combination, in adults with varying degrees of hepatic impairment, including cirrhosis. This research is significant as it seeks to understand how these drugs behave in patients with liver conditions, potentially informing future treatments.
Vir Biotechnology’s recent earnings call presented a balanced sentiment, highlighting significant progress in their clinical programs and financial management. Despite operating at a loss and experiencing substantial cash consumption, the company showcased advancements in its hepatitis delta and oncology programs, alongside improvements in cost efficiency, contributing to an optimistic outlook.
Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on developing medicines for serious infectious diseases and cancer, with a unique emphasis on leveraging the immune system to transform lives.