| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 3.15B | 2.75B | 3.82B | 17.31B | 18.98B | 482.30M |
| Gross Profit | 2.60B | 2.21B | 3.22B | 14.32B | 16.07B | 423.00M |
| EBITDA | -103.30M | -367.10M | 1.38B | 13.10B | 15.00B | -105.10M |
| Net Income | -571.60M | -665.30M | 930.30M | 9.43B | 10.29B | 15.20M |
Balance Sheet | ||||||
| Total Assets | 21.34B | 22.53B | 23.01B | 23.28B | 15.83B | 2.32B |
| Cash, Cash Equivalents and Short-Term Investments | 14.53B | 16.78B | 16.55B | 14.06B | 2.07B | 1.35B |
| Total Debt | 245.40M | 254.20M | 219.10M | 212.20M | 301.50M | 240.10M |
| Total Liabilities | 2.86B | 3.12B | 2.76B | 3.22B | 3.94B | 946.80M |
| Stockholders Equity | 18.48B | 19.41B | 20.25B | 20.06B | 11.89B | 1.37B |
Cash Flow | ||||||
| Free Cash Flow | -1.09B | -244.60M | 4.67B | 13.21B | 735.70M | -98.90M |
| Operating Cash Flow | -316.80M | 207.70M | 5.37B | 13.58B | 889.70M | -13.50M |
| Investing Cash Flow | 863.80M | -2.08B | -6.95B | -35.30M | -566.10M | -144.80M |
| Financing Cash Flow | -45.90M | -45.90M | -778.60M | -1.42B | 94.20M | 894.70M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
76 Outperform | $55.52B | 41.80 | 24.75% | ― | 89.58% | ― | |
76 Outperform | $18.78B | 12.83 | 28.20% | ― | 24.98% | 127.06% | |
61 Neutral | ― | ― | ― | ― | 730.42% | 31.63% | |
57 Neutral | $59.81B | 1,883.28 | 32.73% | ― | 53.24% | ― | |
53 Neutral | $26.86B | ― | -2.94% | ― | 7.04% | -25.24% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $9.67B | ― | -29.32% | ― | -56.00% | -38.95% |
On November 11, 2025, BioNTech SE hosted its Innovation Series R&D Day, where it outlined its strategic direction and clinical advancements across its pipeline. The event highlighted BioNTech’s unique approach to innovation and its differentiated clinical strategy in oncology, including the development of mRNA cancer immunotherapies. The presentation emphasized the company’s ongoing efforts to establish Pumitamig1 in foundational tumor types and its partnership with Bristol Myers Squibb. This event reflects BioNTech’s commitment to advancing cancer treatment and its continued impact on the biotechnology industry.
On November 3, 2025, BioNTech SE announced its third-quarter financial results, highlighting a revenue increase to €1.5 billion, despite a net loss of €28.7 million. The company reported progress in its oncology strategy, particularly with the bispecific antibody candidate pumitamig, and launched a variant-adapted COVID-19 vaccine for the 2025/2026 season. BioNTech also raised its full-year revenue guidance to €2.6-2.8 billion, supported by a $1.5 billion payment from its partnership with Bristol Myers Squibb.
On November 3, 2025, BioNTech SE announced its financial results for the three and nine months ending September 30, 2025. The company reported revenues of €1,518.9 million for the third quarter, reflecting a significant increase from the previous year. However, despite the revenue growth, BioNTech experienced an operating loss of €46.9 million for the quarter, attributed to increased research and development expenses and other operating costs. This financial update highlights the company’s ongoing investment in its pipeline and the challenges of balancing revenue growth with operational costs.
On October 22, 2025, BioNTech SE announced the commencement of a public exchange offer for all outstanding shares of CureVac N.V., as part of a strategic acquisition to enhance its capabilities in mRNA-based cancer immunotherapy. This acquisition is expected to strengthen BioNTech’s research, development, manufacturing, and commercialization efforts, marking a significant milestone in its oncology strategy. The transaction, valued at approximately $1.25 billion, aims to create long-term value for shareholders and advance the development of innovative cancer treatments.
On October 1, 2025, BioNTech SE, in collaboration with InstaDeep Ltd., hosted its second AI Day as part of its Innovation Series. The event highlighted BioNTech’s AI strategy and its application in the company’s pipeline and internal processes. This initiative underscores BioNTech’s commitment to leveraging AI to advance its position in the biotechnology industry, potentially impacting its operational efficiency and stakeholder engagement.
On September 8, 2025, BioNTech SE and Bristol Myers Squibb presented interim data from a Phase 2 trial evaluating pumitamig, a bispecific antibody, in patients with extensive-stage small cell lung cancer. The data showed promising antitumor activity, with a 76.3% confirmed objective response rate and a 100% disease control rate, suggesting potential for pumitamig to become a new standard of care in this aggressive cancer type. The trial’s results are being used to inform a global Phase 3 trial, and pumitamig has received Orphan Drug designation from the FDA.
On June 2, 2025, BioNTech SE entered into a Global Co-Development and Co-Commercialization Agreement with Bristol-Myers Squibb Company to develop, manufacture, and commercialize the bispecific antibody BNT327 for various solid tumor types. The agreement, which was amended on August 15, 2025, includes a $1.5 billion upfront payment to BioNTech and up to $7.6 billion in additional milestone payments. The collaboration will see both companies sharing profits and losses equally, with a focus on maximizing the success and efficiency of BNT327’s development and commercialization. This strategic partnership is expected to enhance BioNTech’s position in the oncology market and provide significant financial benefits.
On September 5, 2025, BioNTech SE and Duality Biologics announced that their Phase 3 trial in China for trastuzumab pamirtecan (BNT323/DB-1303) met its primary endpoint of progression-free survival in patients with HER2-positive metastatic breast cancer. This milestone marks the first positive Phase 3 data from their strategic collaboration, highlighting the potential of trastuzumab pamirtecan as a new treatment option. The success of this trial strengthens BioNTech’s position in oncology and supports further development of the drug in other regions, including the U.S. and EU.
On August 27, 2025, BioNTech SE and Pfizer Inc. announced that the U.S. Food and Drug Administration approved their LP.8.1-adapted monovalent COVID-19 vaccine, COMIRNATY® LP.8.1, for adults aged 65 and older, and individuals aged 5 through 64 with underlying conditions at high risk for severe COVID-19 outcomes. This approval is based on extensive clinical and real-world data demonstrating the vaccine’s safety and efficacy. The vaccine targets the SARS-CoV-2 sublineage LP.8.1, aligning with FDA guidance to address circulating strains. Shipping of the vaccine will commence immediately to ensure availability in pharmacies, hospitals, and clinics across the U.S., reinforcing BioNTech’s and Pfizer’s positions in the vaccine market and their commitment to addressing public health needs.