| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 447.02M | 363.71M | 305.21M | 245.36M | 188.46M | 164.41M |
| Gross Profit | 312.79M | 277.96M | 239.63M | 190.23M | 144.31M | 124.54M |
| EBITDA | -1.09B | -818.79M | -660.18M | -447.37M | -383.65M | -250.37M |
| Net Income | -1.18B | -913.77M | -749.57M | -481.53M | -434.65M | -294.09M |
Balance Sheet | ||||||
| Total Assets | 2.36B | 2.03B | 1.33B | 1.66B | 1.24B | 796.15M |
| Cash, Cash Equivalents and Short-Term Investments | 1.68B | 1.43B | 780.45M | 1.15B | 716.78M | 532.76M |
| Total Debt | 745.08M | 1.31B | 1.20B | 1.18B | 612.27M | 404.84M |
| Total Liabilities | 1.42B | 1.74B | 1.66B | 1.57B | 833.04M | 520.27M |
| Stockholders Equity | 945.57M | 285.38M | -331.92M | 87.95M | 410.47M | 275.88M |
Cash Flow | ||||||
| Free Cash Flow | -906.14M | -705.80M | -549.53M | -410.32M | -370.59M | -226.17M |
| Operating Cash Flow | -883.40M | -683.88M | -536.25M | -400.44M | -363.30M | -219.35M |
| Investing Cash Flow | -322.23M | -583.17M | -223.60M | -34.58M | -64.28M | -6.82M |
| Financing Cash Flow | 1.08B | 1.34B | 168.44M | 793.27M | 612.55M | 271.00M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
81 Outperform | $20.13B | 16.22 | 30.39% | ― | 18.09% | 3563.21% | |
79 Outperform | $22.32B | 22.11 | 11.51% | 2.31% | 3.72% | -31.46% | |
77 Outperform | $10.26B | 19.97 | 9.07% | ― | 12.31% | 60.21% | |
76 Outperform | $19.52B | 13.45 | 28.20% | ― | 24.98% | 127.06% | |
54 Neutral | $43.51B | ― | -165.69% | ― | 30.34% | -11.26% | |
53 Neutral | $23.39B | ― | -2.94% | ― | 7.04% | -25.24% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
On November 18, 2025, Insmed announced that the European Commission approved BRINSUPRI (brensocatib 25 mg tablets) for treating non-cystic fibrosis bronchiectasis (NCFB) in patients aged 12 and older with two or more exacerbations in the past year. This approval marks a significant milestone as BRINSUPRI becomes the first and only approved treatment for NCFB in the EU, potentially reshaping the treatment landscape for this debilitating disease. The decision was based on data from the Phase 3 ASPEN and Phase 2 WILLOW studies, which demonstrated a reduction in exacerbations and a slower decline in lung function. Insmed plans to engage with EU authorities to secure access for eligible patients starting in early 2026.