Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 398.11M | 363.71M | 305.21M | 245.36M | 188.46M | 164.41M |
Gross Profit | 300.17M | 277.96M | 239.63M | 190.23M | 144.31M | 124.54M |
EBITDA | -934.78M | -814.14M | -660.18M | -429.44M | -375.09M | -250.37M |
Net Income | -1.03B | -913.77M | -749.57M | -481.53M | -434.65M | -294.09M |
Balance Sheet | ||||||
Total Assets | 2.48B | 2.03B | 1.33B | 1.66B | 1.24B | 796.15M |
Cash, Cash Equivalents and Short-Term Investments | 1.86B | 1.43B | 780.45M | 1.15B | 716.78M | 532.76M |
Total Debt | 575.51M | 1.15B | 1.20B | 1.18B | 612.27M | 404.84M |
Total Liabilities | 1.23B | 1.74B | 1.66B | 1.57B | 833.04M | 520.27M |
Stockholders Equity | 1.25B | 285.38M | -331.92M | 87.95M | 410.47M | 275.88M |
Cash Flow | ||||||
Free Cash Flow | -868.57M | -705.80M | -549.53M | -410.32M | -370.59M | -226.17M |
Operating Cash Flow | -844.55M | -683.88M | -536.25M | -400.44M | -363.30M | -219.35M |
Investing Cash Flow | -563.47M | -583.17M | -223.60M | -34.58M | -64.28M | -6.82M |
Financing Cash Flow | 1.44B | 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 |
---|---|---|---|---|---|---|---|
82 Outperform | $16.85B | 13.64 | 26.08% | ― | 23.25% | 64.46% | |
80 Outperform | $16.68B | 19.70 | 24.30% | ― | 18.87% | 1088.27% | |
76 Outperform | $10.90B | 16.81 | 11.62% | ― | 17.38% | 153.58% | |
72 Outperform | $21.52B | 15.96 | 15.92% | 2.41% | 3.04% | 53.03% | |
63 Neutral | $30.13B | ― | -160.54% | ― | 21.15% | -5.65% | |
55 Neutral | $24.88B | ― | -1.81% | ― | 7.51% | 30.53% | |
51 Neutral | $7.92B | -0.43 | -41.67% | 2.21% | 22.29% | -1.85% |
On August 12, 2025, Insmed announced that the FDA approved BRINSUPRI, the first and only treatment for non-cystic fibrosis bronchiectasis (NCFB) in patients 12 years and older. This approval marks a significant advancement for the approximately 500,000 U.S. patients diagnosed with NCFB, offering a new standard of care by targeting neutrophilic inflammation, a root cause of the disease. The approval is based on positive results from the Phase 3 ASPEN and Phase 2 WILLOW studies, which demonstrated reductions in exacerbations and improvements in lung function. The approval is expected to have a substantial impact on Insmed’s operations and industry positioning, as it addresses a previously unmet need in the treatment of NCFB.
On June 11, 2025, Insmed announced the commencement and pricing of a public offering of its common stock, aiming to raise $650 million, with an option for underwriters to purchase additional shares. The offering, managed by Goldman Sachs and Leerink Partners, is expected to generate approximately $716.3 million in net proceeds, potentially impacting Insmed’s financial position and market operations.
On June 10, 2025, Insmed announced positive topline results from its Phase 2b study of treprostinil palmitil inhalation powder (TPIP) in patients with pulmonary arterial hypertension. The study, which met its primary and all secondary efficacy endpoints, demonstrated a 35% placebo-adjusted reduction in pulmonary vascular resistance and significant improvements in other key metrics. These results underscore TPIP’s potential as a highly effective, once-daily prostanoid therapy. Following these findings, Insmed plans to engage with the FDA to design a Phase 3 trial and aims to initiate further studies in late 2025 and early 2026. The announcement marks a significant advancement in PAH treatment, potentially impacting the company’s market positioning and offering new hope for patients.