| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 42.34M | 43.27M | 46.02M | 41.40M | 36.94M | 34.44M |
| Gross Profit | 39.83M | 39.56M | 41.39M | 33.08M | 28.76M | 28.61M |
| EBITDA | -210.01M | -129.23M | -69.00M | -96.62M | -50.15M | -35.49M |
| Net Income | -205.75M | -130.87M | -70.80M | -102.25M | -58.42M | -45.39M |
Balance Sheet | ||||||
| Total Assets | 251.69M | 418.46M | 355.18M | 180.36M | 263.37M | 91.72M |
| Cash, Cash Equivalents and Short-Term Investments | 204.02M | 370.91M | 331.05M | 144.56M | 211.56M | 44.91M |
| Total Debt | 21.30M | 21.86M | 4.91M | 46.35M | 39.20M | 40.99M |
| Total Liabilities | 51.51M | 81.96M | 88.86M | 83.99M | 78.99M | 73.18M |
| Stockholders Equity | 200.18M | 336.50M | 266.32M | 96.37M | 184.38M | 18.54M |
Cash Flow | ||||||
| Free Cash Flow | -213.59M | -130.28M | -1.61M | -67.16M | -50.25M | -14.80M |
| Operating Cash Flow | -210.91M | -126.23M | 1.88M | -65.00M | -50.10M | -14.44M |
| Investing Cash Flow | 47.28M | -219.35M | -3.31M | -17.27M | -33.12M | -362.00K |
| Financing Cash Flow | 158.38M | 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 |
|---|---|---|---|---|---|---|---|
70 Outperform | $1.85B | 49.98 | 15.02% | ― | 1128.17% | ― | |
66 Neutral | $1.18B | 1,130.56 | 0.44% | ― | 26.54% | ― | |
59 Neutral | $1.26B | -9.95 | -51.65% | ― | 53.28% | 21.77% | |
58 Neutral | $1.32B | -5.48 | -98.23% | ― | -7.38% | -49.03% | |
54 Neutral | $717.98M | -4.21 | -611.42% | ― | 96.83% | -61.92% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $1.02B | -6.60 | ― | ― | 8.00% | -10.15% |
On December 8, 2025, EyePoint, Inc. officially changed its name from EyePoint Pharmaceuticals, Inc. This change, which also involved amendments to the company’s by-laws, does not impact the trading of its common stock on the Nasdaq Global Market under the ticker symbol ‘EYPT’, nor does it affect the rights of the company’s security holders.
On November 19, 2025, EyePoint Pharmaceuticals announced a positive recommendation from the independent Data Safety Monitoring Committee for its ongoing pivotal Phase 3 trials of DURAVYU for treating wet age-related macular degeneration (wet AMD). The trials, named LUGANO and LUCIA, have shown no safety signals, and the DSMC recommended continuing without protocol changes. This strengthens confidence in DURAVYU’s safety profile, with topline data expected in mid-2026. The trials are significant as they evaluate a sustained release treatment potentially reducing the treatment burden for wet AMD, a condition requiring frequent interventions.
On November 6, 2025, EyePoint Pharmaceuticals filed a prospectus supplement to its registration statement with the SEC, enabling a registered offering of up to $200 million in common stock. This move, under the Controlled Equity Offering Sales Agreement with Cantor Fitzgerald & Co., signifies a strategic financial maneuver to potentially enhance the company’s capital, impacting its market positioning and stakeholder interests.
On October 14, 2025, EyePoint Pharmaceuticals announced an underwritten public offering of 11,000,000 shares of its common stock and pre-funded warrants for 1,500,000 shares, raising approximately $141 million. The offering, which closed on October 16, 2025, aims to fund the clinical development of DURAVYU™ and support pipeline initiatives. This move is expected to bolster EyePoint’s financial position and advance its strategic objectives in the biopharmaceutical industry.
On October 14, 2025, EyePoint Pharmaceuticals announced the initiation of its pivotal Phase 3 program for DURAVYU, targeting diabetic macular edema (DME), with first patient dosing expected in Q1 2026. The program follows a non-inferiority approval pathway and includes two trials, COMO and CAPRI, each enrolling approximately 240 patients. New preclinical data highlights DURAVYU’s potential as a multi-mechanism treatment, inhibiting both VEGF-mediated vascular permeability and IL-6 mediated inflammation, which are key contributors to DME and wet AMD. This advancement positions DURAVYU as a promising option for addressing the multifactorial nature of DME and reducing treatment burdens for patients.