Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 56.04M | 43.27M | 46.02M | 41.40M | 36.94M | 34.44M |
Gross Profit | 52.28M | 39.56M | 41.39M | 33.08M | 28.76M | 28.61M |
EBITDA | -148.59M | -129.23M | -69.00M | -96.62M | -50.15M | -35.49M |
Net Income | -146.78M | -130.87M | -70.80M | -124.51M | -63.91M | -52.65M |
Balance Sheet | ||||||
Total Assets | 362.56M | 418.46M | 355.18M | 180.36M | 263.37M | 91.72M |
Cash, Cash Equivalents and Short-Term Investments | 318.19M | 370.91M | 331.05M | 144.56M | 211.56M | 44.91M |
Total Debt | 24.08M | 21.86M | 4.91M | 45.77M | 38.42M | 40.31M |
Total Liabilities | 64.17M | 81.96M | 88.86M | 83.99M | 78.99M | 73.18M |
Stockholders Equity | 298.40M | 336.50M | 266.32M | 96.37M | 184.38M | 18.54M |
Cash Flow | ||||||
Free Cash Flow | -151.31M | -130.28M | -1.61M | -67.16M | -50.25M | -14.80M |
Operating Cash Flow | -148.18M | -126.23M | 1.88M | -65.00M | -50.10M | -14.44M |
Investing Cash Flow | -200.64M | -219.35M | -3.31M | -17.27M | -33.12M | -362.00K |
Financing Cash Flow | 162.96M | 164.02M | 187.07M | -690.00K | 216.90M | 37.49M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
68 Neutral | $1.03B | 22.33 | 18.17% | ― | 1218.82% | ― | |
67 Neutral | $934.06M | ― | -3.40% | ― | 22.68% | 42.45% | |
55 Neutral | $798.87M | ― | -73.95% | ― | 2.99% | -49.11% | |
54 Neutral | $855.89M | ― | -452.20% | ― | 10.85% | -1.41% | |
51 Neutral | $7.78B | -0.06 | -40.08% | 2.29% | 21.32% | -1.82% | |
47 Neutral | $767.70M | ― | -76.09% | ― | -42.84% | -17.32% | |
41 Neutral | $609.79M | ― | -379.53% | ― | 366.84% | -35.87% |
On July 29, 2025, EyePoint Pharmaceuticals announced the completion of enrollment for its Phase 3 pivotal trials, LUGANO and LUCIA, evaluating DURAVYU for wet AMD. The trials enrolled over 800 patients, marking one of the fastest enrollments for such programs. Interim safety data confirmed DURAVYU’s favorable safety profile, with no serious adverse events related to the drug. The trials are designed to support regulatory approval and aim to reduce treatment burden with a 6-month redosing schedule, potentially shifting the treatment paradigm for wet AMD.
On June 18, 2025, EyePoint Pharmaceuticals held its Annual Meeting of Stockholders via webcast, where stockholders approved an amendment to increase the number of shares in the 2023 Long-Term Incentive Plan by 2,900,000 shares. Additionally, the meeting included the election of directors, approval of executive compensation, and ratification of Deloitte & Touche LLP as the independent auditor, reflecting strong shareholder engagement and strategic alignment with the company’s growth objectives.
On May 27, 2025, EyePoint Pharmaceuticals announced the completion of patient enrollment in the Phase 3 LUGANO clinical trial for DURAVYU, a treatment for wet age-related macular degeneration (wet AMD). This milestone was achieved with over 400 patients enrolled in seven months, marking one of the fastest enrollments for a Phase 3 trial in wet AMD. The trial’s rapid progress reflects strong interest from both patients and physicians, highlighting the commercial potential of DURAVYU. The LUGANO trial, along with the ongoing LUCIA trial, aims to assess the efficacy and safety of DURAVYU, with topline data expected in mid-2026. The trials are designed to evaluate the potential of DURAVYU to transform treatment paradigms for wet AMD, offering a sustained-release option that could reduce treatment burdens and improve patient compliance.