Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
144.28M | 127.04M | 107.67M | 86.35M | 88.64M | Gross Profit |
105.64M | 61.94M | 52.80M | 40.33M | 52.45M | EBIT |
-11.53M | -110.61M | -174.66M | -217.83M | -228.16M | EBITDA |
-5.06M | -103.79M | -176.66M | -215.25M | -222.53M | Net Income Common Stockholders |
-13.58M | -110.56M | -134.52M | -217.66M | -224.43M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
59.28M | 80.41M | 84.85M | 157.58M | 208.49M | Total Assets |
233.15M | 222.51M | 250.95M | 305.71M | 353.56M | Total Debt |
177.76M | 179.63M | 157.48M | 159.50M | 24.61M | Net Debt |
151.96M | 150.95M | 142.11M | 68.95M | -80.53M | Total Liabilities |
266.80M | 256.48M | 237.38M | 228.14M | 117.06M | Stockholders Equity |
-33.65M | -33.97M | 13.57M | 77.57M | 236.49M |
Cash Flow | Free Cash Flow | |||
-24.23M | -60.33M | -148.74M | -206.38M | -191.63M | Operating Cash Flow |
-22.53M | -58.79M | -146.91M | -203.35M | -184.82M | Investing Cash Flow |
18.71M | 18.00M | -3.32M | 32.73M | 208.96M | Financing Cash Flow |
940.00K | 54.11M | 75.06M | 156.03M | 9.11M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
53 Neutral | $5.14B | 3.06 | -43.57% | 2.81% | 16.81% | -0.12% | |
50 Neutral | $292.92M | ― | 40.36% | ― | 12.43% | 91.67% | |
49 Neutral | $282.37M | ― | -152.14% | ― | 22.16% | -37.60% | |
48 Neutral | $491.14M | ― | ― | ― | ― | ||
42 Neutral | $458.60M | ― | -30.10% | ― | ― | -343.40% | |
38 Underperform | $480.26M | ― | -115.47% | ― | ― | ― | |
36 Underperform | $253.73M | ― | -59.60% | ― | -100.00% | 31.43% |
On May 6, 2025, Heron Therapeutics announced a settlement agreement with Mylan Pharmaceuticals to resolve patent litigations concerning CINVANTI® and APONVIE® injectable emulsions in the U.S. District Court for the District of Delaware. As part of the settlement, Heron granted Mylan a license to market generic versions of these products in the U.S. starting June 1, 2032, or earlier under certain conditions. The litigations were initiated by Heron in response to Mylan’s applications for FDA approval of generic versions before the expiration of Heron’s patents in 2035. This agreement will lead to the dismissal of the pending litigations, potentially impacting Heron’s market exclusivity and future revenue streams.
On April 28, 2025, Heron Therapeutics announced the appointment of Mark Hensley as Chief Operating Officer. Mr. Hensley, who has over fifteen years of experience in the pharmaceutical industry, previously held senior leadership roles at Veloxis Pharmaceuticals. His appointment is expected to play a pivotal role in Heron’s growth, with his extensive operational and leadership experience ensuring efficiency and compliance as the company advances its strategic priorities. Mr. Hensley’s compensation includes a base salary, a cash bonus, and inducement awards in the form of stock options and restricted stock units, which are designed to align his interests with the company’s performance goals.