| Breakdown | Dec 2025 | Dec 2024 | Dec 2023 | Mar 2023 | Dec 2021 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 22.50M | 45.56M | 14.09M | 102.69M | 0.00 |
| Gross Profit | 22.44M | 45.56M | 14.09M | 102.69M | 0.00 |
| EBITDA | -242.32M | -241.49M | -176.86M | -22.34M | -41.37M |
| Net Income | -203.82M | -241.60M | -176.94M | -22.63M | -41.78M |
Balance Sheet | |||||
| Total Assets | 769.28M | 864.62M | 347.10M | 478.50M | 67.99M |
| Cash, Cash Equivalents and Short-Term Investments | 636.24M | 834.19M | 340.45M | 467.73M | 60.38M |
| Total Debt | 202.00K | 448.00K | 60.00K | 126.00K | 186.51K |
| Total Liabilities | 85.85M | 107.12M | 58.70M | 48.43M | 11.36M |
| Stockholders Equity | 683.43M | 757.50M | 288.39M | 430.07M | 56.63M |
Cash Flow | |||||
| Free Cash Flow | -148.03M | -159.24M | -141.24M | 10.44M | -29.54M |
| Operating Cash Flow | -147.78M | -158.56M | -141.22M | 10.66M | -29.51M |
| Investing Cash Flow | -174.92M | -62.85M | -24.00K | -221.00K | -24.00K |
| Financing Cash Flow | 29.52M | 659.51M | 8.91M | 391.90M | 84.70M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
69 Neutral | $3.52B | 61.71 | 11.73% | ― | 55.68% | ― | |
66 Neutral | $2.02B | 175.24 | 5.89% | ― | ― | 44.84% | |
63 Neutral | $3.54B | -9.76 | -51.76% | ― | ― | -38.30% | |
62 Neutral | $5.65B | -10.35 | -69.35% | ― | ― | -27.70% | |
55 Neutral | $3.77B | -18.79 | -28.29% | ― | ― | ― | |
52 Neutral | $3.85B | -10.47 | -47.34% | ― | ― | -126.16% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
On March 2, 2026, NewAmsterdam Pharma posted an updated corporate investor presentation detailing recent clinical, commercial, and financial progress around its lead candidate obicetrapib. The company highlighted Phase 2 and Phase 3 data indicating significant LDL-C reductions of roughly 35–40% as monotherapy and about 50% in combination with ezetimibe, plus a roughly 45% cut in Lp(a) and a 21% exploratory one-year MACE reduction favoring obicetrapib, alongside broader biomarker effects including ApoB, non-HDL-C, LDL-P, HDL-C, and markers of glycemic control and renal function.
The presentation underscored obicetrapib’s potential to serve a substantial cardiometabolic market, especially the approximately 30 million U.S. patients on lipid-lowering drugs who remain above LDL-C goals due to product limitations and access hurdles. Management also pointed to strengthened fundamentals, including comprehensive patent protection until mid-2043, publication of key BROOKLYN, BROADWAY and TANDEM Phase 3 results in leading journals, expansion of commercial and medical affairs infrastructure in Europe and the U.S., and an expected year-end 2025 cash balance of about $729 million intended to support a prospective U.S. launch and regulatory milestones such as a planned EMA submission in 2025.
The most recent analyst rating on (NAMS) stock is a Buy with a $52.00 price target. To see the full list of analyst forecasts on NewAmsterdam Pharma Company stock, see the NAMS Stock Forecast page.
On January 9, 2026, NewAmsterdam Pharma highlighted its 2025 clinical and regulatory progress for obicetrapib and set out key goals for 2026, underscoring its push toward commercialization in cardiovascular disease and potential expansion into neurodegeneration. In 2025, the company reported statistically significant reductions in Alzheimer’s disease biomarker p-tau217 from the Phase 3 BROADWAY trial, presented pooled Phase 3 efficacy and safety data for obicetrapib at major cardiology forums, and secured EMA validation of marketing applications for obicetrapib monotherapy and an obicetrapib/ezetimibe fixed-dose combination in hypercholesterolemia, with a European approval decision anticipated in the second half of 2026. Operationally, NewAmsterdam advanced three Phase 3 programs—PREVAIL, REMBRANDT and RUBENS—completed PREVAIL enrollment at over 9,500 patients, began RUBENS enrollment in December 2025, and plans to launch a dedicated early Alzheimer’s disease trial in 2026, leveraging emerging links between CETP inhibition and neurodegeneration. With approximately $729 million in unaudited cash, cash equivalents and marketable securities at year-end 2025, the company expects to be funded through the PREVAIL cardiovascular outcomes readout and a potential subsequent U.S. commercial launch, positioning it as a significant emerging player in the crowded LDL-C–lowering market and offering potential upside for partners and future shareholders if pivotal data and regulatory reviews are favorable.
The most recent analyst rating on (NAMS) stock is a Buy with a $45.00 price target. To see the full list of analyst forecasts on NewAmsterdam Pharma Company stock, see the NAMS Stock Forecast page.