Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 47.14M | 45.56M | 12.76M | 95.91M | 0.00 | 0.00 |
Gross Profit | 47.14M | 45.56M | 12.76M | 95.91M | 0.00 | 0.00 |
EBITDA | -255.78M | -241.49M | -176.86M | -3.31M | -30.73M | -5.43M |
Net Income | -187.36M | -241.60M | -176.94M | -21.14M | -36.71M | -5.75M |
Balance Sheet | ||||||
Total Assets | 818.41M | 864.62M | 347.10M | 531.58M | 59.78M | 9.23M |
Cash, Cash Equivalents and Short-Term Investments | 808.48M | 834.19M | 340.45M | 438.52M | 53.09M | 7.86M |
Total Debt | 389.00K | 448.00K | 60.00K | 118.00K | 164.00K | 11.65M |
Total Liabilities | 41.05M | 107.12M | 58.70M | 47.06M | 9.99M | 12.81M |
Stockholders Equity | 777.36M | 757.50M | 288.39M | 484.52M | 49.79M | -3.58M |
Cash Flow | ||||||
Free Cash Flow | -86.55M | -159.24M | -141.24M | 7.96M | -25.18M | -5.98M |
Operating Cash Flow | -136.75M | -158.56M | -141.22M | 7.97M | -25.16M | -5.97M |
Investing Cash Flow | -59.40M | -62.85M | -24.00K | 715.00K | -20.00K | -13.00K |
Financing Cash Flow | 467.53M | 659.51M | 8.91M | 375.18M | 68.99M | 11.32M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
78 Outperform | $2.13B | 12.10 | 27.58% | ― | 17.74% | 59.96% | |
61 Neutral | $2.77B | ― | -28.43% | ― | ― | ― | |
58 Neutral | $1.84B | ― | -57.33% | ― | 99.50% | 65.91% | |
51 Neutral | $7.91B | -0.36 | -41.71% | 2.23% | 23.45% | -1.86% | |
50 Neutral | $2.03B | ― | -86.34% | ― | 30.14% | -10.08% | |
45 Neutral | $2.26B | ― | -39.69% | ― | -100.00% | 1.62% | |
40 Underperform | $3.80B | ― | ― | ― | ― |
On September 2, 2025, NewAmsterdam Pharma Company released an updated corporate investor presentation highlighting significant progress in its clinical trials for obicetrapib, a promising treatment for lowering LDL-C levels. The presentation detailed the company’s strategic plans, including securing funding for a potential U.S. commercial launch and expanding its workforce. The company’s trials have shown favorable results, indicating a substantial market opportunity, particularly in the U.S., where many patients are not meeting cholesterol goals with existing treatments.
On August 18, 2025, NewAmsterdam Pharma announced that the European Medicines Agency has validated the Marketing Authorization Application for obicetrapib, both as a monotherapy and in combination with ezetimibe, for treating primary hypercholesterolemia and mixed dyslipidemia. This validation marks a significant step for NewAmsterdam, allowing the EMA to review pivotal Phase 3 trials, which demonstrated substantial LDL-C reductions. The company, in partnership with Menarini, aims to bring this novel treatment to Europe, potentially offering a new therapeutic option for patients not meeting LDL-C goals despite existing treatments.
On August 12, 2025, NewAmsterdam Pharma’s subsidiary entered into a Supply Agreement with A. Menarini International Licensing S.A. to supply obicetrapib monotherapy and combination drug products. The agreement outlines NewAmsterdam Pharma as the exclusive supplier initially, with plans to transfer manufacturing to Menarini or a third party, impacting the company’s operational dynamics and industry positioning.
On July 30, 2025, NewAmsterdam Pharma announced promising results from its Phase 3 BROADWAY clinical trial, which evaluated the effects of obicetrapib on Alzheimer’s disease biomarkers. The trial showed that obicetrapib significantly reduced levels of plasma p-tau217, a key biomarker of Alzheimer’s pathology, especially in ApoE4 carriers, a group at heightened risk for the disease. These findings suggest that obicetrapib could offer a novel approach to Alzheimer’s prevention while also providing cardiovascular benefits, positioning the company as a potential leader in addressing both neurodegenerative and cardiovascular diseases.
On July 11, 2025, NewAmsterdam Pharma B.V. updated its Employment Agreement with Dr. John Kastelein, effective July 1, 2025. This agreement outlines severance and benefits for Dr. Kastelein in cases of employment termination without cause or due to a change in control, impacting his stock options and equity awards.
NewAmsterdam Pharma Company announced a Research & Development Day event scheduled for June 11, 2025, in New York City, aimed at analysts and investors. The event will be webcast live, with a replay available for 30 days. The company has been active in clinical trials, with significant developments in its BROOKLYN, BROADWAY, and TANDEM Phase 3 studies, and has secured funding to support a potential U.S. commercial launch. The company’s product candidate, Obicetrapib, shows promise in addressing cardiometabolic diseases, and there are ongoing efforts to explore its therapeutic potential in Alzheimer’s disease and multi-infarct dementia.
On June 9, 2025, NewAmsterdam Pharma announced positive topline data from their Phase 3 BROADWAY clinical trial, which evaluated the effects of obicetrapib on Alzheimer’s Disease biomarkers. The study showed statistically significant reductions in the primary outcome measure of p-tau217 in both the full study population and ApoE4 carriers, suggesting a potential preventive strategy for Alzheimer’s Disease. These findings highlight the potential of CETP inhibition in mitigating Alzheimer’s risk and further differentiate obicetrapib as a uniquely effective therapy addressing multiple health concerns, including cardiovascular and neurodegenerative diseases.
On June 4, 2025, NewAmsterdam Pharma Company N.V. held its annual general meeting where 74.45% of eligible shares voted. Shareholders approved several proposals, including the adoption of the 2024 annual accounts, discharge of directors’ liabilities, appointment of Deloitte as auditor, and various board appointments. The company also decided to hold annual Say-on-Pay votes until 2031.