| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 571.16M | 489.68M | 91.43M | 83.03M | 36.77M | 66.62M |
| Gross Profit | 316.53M | 304.37M | -69.42M | 18.93M | 36.77M | 66.62M |
| EBITDA | 72.66M | -32.27M | -493.67M | -439.80M | -18.03M | -177.88M |
| Net Income | 69.53M | -231.86M | -551.73M | -513.58M | -101.50M | -170.04M |
Balance Sheet | ||||||
| Total Assets | 1.41B | 1.22B | 950.09M | 828.44M | 597.98M | 474.42M |
| Cash, Cash Equivalents and Short-Term Investments | 42.85M | 51.43M | 11.16M | 66.43M | 17.56M | 31.69M |
| Total Debt | 1.28B | 1.19B | 1.08B | 805.10M | 523.05M | 676.85M |
| Total Liabilities | 1.59B | 1.63B | 1.88B | 1.39B | 733.59M | 1.34B |
| Stockholders Equity | -176.76M | -412.77M | -932.49M | -564.42M | -135.61M | -867.24M |
Cash Flow | ||||||
| Free Cash Flow | -113.45M | -293.84M | -358.66M | -361.39M | -268.80M | -86.28M |
| Operating Cash Flow | -26.49M | -236.84M | -312.19M | -312.39M | -228.17M | -74.30M |
| Investing Cash Flow | -119.50M | -18.87M | -46.34M | -63.54M | -40.63M | -16.90M |
| Financing Cash Flow | 68.36M | 297.31M | 301.32M | 424.91M | 254.83M | 55.40M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
64 Neutral | $1.80B | 49.26 | 7.83% | ― | 48.87% | ― | |
63 Neutral | $3.56B | 788.19 | ― | ― | 9.50% | ― | |
55 Neutral | $2.59B | ― | -1.86% | ― | 4.54% | -130.59% | |
52 Neutral | $2.73B | 5.76 | 47.54% | ― | -1.35% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $2.78B | ― | -0.65% | 5.55% | -2.55% | 66.00% | |
44 Neutral | $1.66B | 23.84 | ― | ― | 55.38% | ― |
On November 20, 2025, Alvotech, in partnership with Advanz Pharma, announced that their biosimilar product Gobivaz®, a version of Simponi® (golimumab), received marketing approval from the European Commission for use in the European Economic Area. This approval marks a significant milestone as Gobivaz® is the first biosimilar to Simponi® approved in Europe, enhancing Alvotech’s commercial presence in the region and expanding access to biologic medicines for immune-mediated diseases. The approval is based on comprehensive analytical and clinical data, further solidifying Alvotech’s position in the biosimilar market.
On November 12, 2025, Alvotech announced its financial results for the first nine months of 2025, reporting a 24% increase in total revenues to $420 million compared to the previous year. Despite a decrease in adjusted EBITDA by 21% due to increased R&D investments, the company revised its full-year revenue outlook to $570-$600 million, anticipating strong growth driven by new biosimilar approvals in Japan and Europe. Alvotech’s strategic focus on expanding its biosimilar portfolio and maintaining operational excellence positions it for continued growth, with significant product launches expected in Q4 2025 and beyond.
On November 10, 2025, Alvotech announced that the UK High Court ruled in its favor, rejecting an injunction request from Regeneron Pharmaceuticals and Bayer. This decision allows Alvotech to continue manufacturing its biosimilar to Eylea (AVT06) in the UK, paving the way for its commercial launch in the European Economic Area and other regions after the expiry of the Supplementary Protection Certificates for Eylea on November 23, 2025. The ruling supports Alvotech’s strategy to enhance access to biosimilars and strengthen its position in the global biosimilar market.
On November 6, 2025, Alvotech announced that the UK Medicines and Healthcare products Regulatory Agency (MHRA) approved its biosimilar to Simponi, named Gobivaz, for various immune-mediated diseases. The approval covers multiple presentations of Gobivaz, enhancing Alvotech’s market positioning by broadening access to biologic treatments in the UK. This development, in partnership with Advanz Pharma, underscores Alvotech’s capabilities in biosimilar development and manufacturing, potentially impacting stakeholders by increasing treatment availability for conditions like rheumatoid arthritis and ulcerative colitis.
On November 2, 2025, Alvotech announced that the U.S. FDA issued a complete response letter for its Biologics License Application for AVT05, a biosimilar candidate to Simponi®. The letter highlighted deficiencies in Alvotech’s Reykjavik facility, which must be resolved before approval. Despite the setback, the facility remains FDA-approved for current products. Alvotech has revised its 2025 financial outlook, anticipating lower revenues and adjusted EBITDA due to ongoing investments in facility improvements, which are expected to support future growth and product launches.
On October 22, 2025, Alvotech announced significant changes to its commercial team, with the departure of Anil Okay, the Chief Commercial Officer, who will become the CEO of Adalvo. Trisha Durant joins as Senior Vice President for Global Business Development and Commercial Operations, excluding North America, while Harshika Sarbajna and Agne Pasko take on key roles in North America and global business development, respectively. These leadership changes are expected to strengthen Alvotech’s commercial operations and strategic partnerships, enhancing its position in the biosimilar industry.
On October 6, 2025, Alvotech announced that the European Medicines Agency accepted a Marketing Authorization Application for AVT23, a proposed biosimilar to Xolair®, developed in collaboration with Kashiv BioSciences LLC. This milestone, in partnership with Advanz Pharma, marks a significant step towards expanding access to affordable biologic medicines for patients in Europe and other regions, potentially enhancing Alvotech’s industry positioning and stakeholder value.
On September 19, 2025, Alvotech announced that its partner in Japan, Fuji Pharma, received marketing authorization for three biosimilars from the Japanese Ministry of Health, Labor and Welfare. These biosimilars, AVT03, AVT05, and AVT06, target bone lesions, rheumatoid arthritis, and macular degeneration, respectively. Additionally, on September 22, 2025, Alvotech announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use recommended approval for AVT03 and AVT05 in the European Economic Area, pending a final decision by the European Commission. These developments are significant for Alvotech’s expansion in the Japanese and European markets, enhancing its industry positioning and offering potential benefits for stakeholders.