| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 | 
|---|---|---|---|---|---|---|
| Income Statement | ||||||
| Total Revenue | 19.32M | 14.00M | 17.49M | 15.94M | 12.85M | 739.63K | 
| Gross Profit | 13.59M | 8.12M | 14.60M | 13.08M | 9.83M | 501.92K | 
| EBITDA | -123.78M | -115.71M | -70.05M | -34.72M | -27.91M | -55.79M | 
| Net Income | -99.89M | -130.39M | -78.50M | -41.02M | -34.58M | -59.76M | 
| Balance Sheet | ||||||
| Total Assets | 257.41M | 230.31M | 118.33M | 129.20M | 93.73M | 99.53M | 
| Cash, Cash Equivalents and Short-Term Investments | 173.42M | 176.48M | 83.68M | 93.28M | 57.49M | 65.32M | 
| Total Debt | 50.91M | 122.39M | 49.54M | 24.46M | 16.08M | 17.14M | 
| Total Liabilities | 242.22M | 153.04M | 71.04M | 38.78M | 28.46M | 28.45M | 
| Stockholders Equity | 15.19M | 77.28M | 47.29M | 90.42M | -309.58M | 71.09M | 
| Cash Flow | ||||||
| Free Cash Flow | -123.98M | -98.37M | -42.85M | -29.18M | -34.14M | -54.90M | 
| Operating Cash Flow | -116.06M | -93.42M | -41.56M | -28.59M | -34.04M | -54.14M | 
| Investing Cash Flow | -7.91M | -8.44M | -11.29M | -587.00K | -107.22K | 247.91K | 
| Financing Cash Flow | 167.80M | 194.66M | 43.25M | 64.96M | 26.32M | 63.42M | 
| Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth | 
|---|---|---|---|---|---|---|---|
| ― | $2.62B | -21.15 | -57.55% | ― | 21.60% | 44.48% | |
| ― | $2.41B | ― | -28.17% | ― | 129.21% | 80.35% | |
| ― | $2.63B | ― | -86.34% | ― | 30.14% | -10.08% | |
| ― | $2.44B | -9.02 | -63.41% | ― | -7.26% | -15.33% | |
| ― | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
| ― | $1.93B | ― | -363.16% | ― | 30.20% | -7.22% | |
| ― | $3.20B | ― | -26.36% | ― | ― | -22.19% | 
Liquidia Technologies is conducting a clinical study titled An Open-Label ProSpective MultiCENTer Study to Evaluate Safety and Tolerability of Dry Powder Inhaled Treprostinil in Pulmonary Hypertension. The study aims to assess the safety and tolerability of LIQ861, a dry powder inhalation form of treprostinil, in patients with pulmonary hypertension (PH) and interstitial lung disease (ILD). This research is significant as it explores a potentially safer and more effective treatment option for these conditions.
The latest earnings call from Liquidia Technologies painted a picture of optimism and growth, with the company showcasing a robust start for its product YUTREPIA. The call highlighted impressive prescription numbers and conversion rates, alongside positive study results and a strong financial standing. However, challenges such as market entry blocks and reliance on channel inventory for initial revenue were also acknowledged.
Liquidia Corporation is a biopharmaceutical company focused on developing innovative therapies for rare cardiopulmonary diseases, leveraging its proprietary PRINT technology to enhance drug delivery and efficacy. In its latest earnings report, Liquidia highlighted the successful commercial launch of YUTREPIA, an inhalation powder for treating pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD), which has seen significant uptake since its FDA approval. The company reported over 900 unique patient prescriptions and 550 patient starts within 11 weeks of launch, reflecting strong demand and the potential for further growth as market access expands. Financially, Liquidia reported product revenue of $6.5 million for the quarter, with a net loss of $41.6 million, driven by increased commercialization efforts and ongoing litigation expenses. Looking ahead, Liquidia aims to scale access to YUTREPIA, expand clinical programs, and continue building value for patients and shareholders, supported by its recent financial agreements.