| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 313.79M | 285.50M | 198.96M | 99.77M | 75.44M | 65.14M |
| Gross Profit | 235.90M | 208.90M | 136.19M | 42.27M | 36.59M | 40.50M |
| EBITDA | 73.13M | 77.47M | 15.13M | -56.32M | -61.10M | -44.66M |
| Net Income | 29.23M | 27.59M | -11.94M | -87.40M | -80.93M | -57.24M |
Balance Sheet | ||||||
| Total Assets | 494.64M | 393.84M | 475.20M | 295.28M | 321.16M | 108.61M |
| Cash, Cash Equivalents and Short-Term Investments | 260.04M | 197.26M | 295.10M | 170.85M | 204.12M | 67.00M |
| Total Debt | 225.95M | 47.70M | 272.62M | 288.40M | 289.22M | 123.44M |
| Total Liabilities | 539.19M | 472.66M | 721.37M | 545.82M | 530.51M | 289.03M |
| Stockholders Equity | -44.55M | -78.82M | -246.17M | -250.54M | -209.35M | -180.42M |
Cash Flow | ||||||
| Free Cash Flow | 43.23M | 32.82M | -8.35M | -88.29M | -73.17M | -32.91M |
| Operating Cash Flow | 48.70M | 42.51M | 34.09M | -80.70M | -61.71M | -28.13M |
| Investing Cash Flow | 35.38M | -96.65M | -1.99M | 4.87M | -151.54M | 15.22M |
| Financing Cash Flow | -19.06M | -137.27M | 136.61M | 21.41M | 270.27M | 49.85M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
64 Neutral | $1.83B | 63.31 | ― | ― | 17.44% | 24.15% | |
55 Neutral | $1.50B | -154.12 | ― | ― | 45.38% | 92.85% | |
53 Neutral | $1.81B | -61.45 | -7.52% | ― | 27.51% | 38.72% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
49 Neutral | $2.22B | -7.03 | -21.37% | ― | 47.15% | -311.26% | |
41 Neutral | $1.71B | -7.48 | -32.44% | ― | -73.94% | -31.70% | |
37 Underperform | $6.00B | -15.99 | -95.40% | ― | ― | 4.32% |
On November 10, 2025, MannKind Corporation announced the discontinuation of its Phase 3 clinical trial for MNKD-101, a nebulized inhalation suspension of clofazimine for treating refractory nontuberculous mycobacterial lung disease. This decision followed the analysis of data from the first 46 participants, which showed no evidence of sputum culture conversion, leading to concerns about achieving the study’s primary endpoint. The data safety monitoring board agreed with the decision due to futility, although no safety issues were found. MannKind plans to investigate the outcome to guide the development of MNKD-102, a dry powder formulation of clofazimine advancing towards Phase 1.
On October 7, 2025, MannKind completed the acquisition of scPharma, making it a wholly-owned subsidiary. This acquisition was facilitated through a merger agreement and involved a contingent value rights agreement, which outlines milestone payments based on FDA approval and sales targets. The acquisition was funded by MannKind’s available cash and borrowings under a credit agreement, with a total transaction cost of approximately $296.5 million. The merger aims to enhance MannKind’s market position by integrating scPharma’s drug-device combination products and leveraging potential sales growth.