| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 51.90M | 43.27M | 46.02M | 41.40M | 36.94M | 34.44M |
| Gross Profit | 49.38M | 39.56M | 41.39M | 33.08M | 28.76M | 28.61M |
| EBITDA | -176.92M | -129.23M | -69.00M | -96.62M | -50.15M | -35.49M |
| Net Income | -175.38M | -130.87M | -70.80M | -102.25M | -58.42M | -45.39M |
Balance Sheet | ||||||
| Total Assets | 301.15M | 418.46M | 355.18M | 180.36M | 263.37M | 91.72M |
| Cash, Cash Equivalents and Short-Term Investments | 255.73M | 370.91M | 331.05M | 144.56M | 211.56M | 44.91M |
| Total Debt | 21.82M | 21.86M | 4.91M | 46.35M | 39.20M | 40.99M |
| Total Liabilities | 55.14M | 81.96M | 88.86M | 83.99M | 78.99M | 73.18M |
| Stockholders Equity | 246.01M | 336.50M | 266.32M | 96.37M | 184.38M | 18.54M |
Cash Flow | ||||||
| Free Cash Flow | -194.04M | -130.28M | -1.61M | -67.16M | -50.25M | -14.80M |
| Operating Cash Flow | -190.59M | -126.23M | 1.88M | -65.00M | -50.10M | -14.44M |
| Investing Cash Flow | 8.10M | -219.35M | -3.31M | -17.27M | -33.12M | -362.00K |
| Financing Cash Flow | 162.87M | 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 |
|---|---|---|---|---|---|---|---|
| ― | $1.77B | 38.20 | 18.17% | ― | 1218.82% | ― | |
| ― | $931.40M | ― | -3.40% | ― | 22.68% | 42.45% | |
| ― | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
| ― | $701.50M | ― | -379.53% | ― | 366.84% | -35.87% | |
| ― | $877.63M | -6.28 | ― | ― | 10.85% | -1.41% | |
| ― | $825.75M | -4.52 | -73.95% | ― | 2.99% | -49.11% | |
| ― | $833.90M | ― | -76.09% | ― | -42.84% | -17.32% |
EyePoint Pharmaceuticals is conducting a Phase 3/4 clinical study titled ‘A Phase 3/4, Prospective, Randomized, Active Treatment-Controlled, Parallel-Design, Multicenter Study to Evaluate the Safety of DEXYCU for the Treatment of Inflammation Following Ocular Surgery for Childhood Cataract.’ The study aims to assess the safety of DEXYCU, a dexamethasone intraocular suspension, in treating inflammation after ocular surgery in children with cataracts, a significant concern in pediatric ophthalmology.
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.
The most recent analyst rating on (EYPT) stock is a Hold with a $11.50 price target. To see the full list of analyst forecasts on EyePoint Pharmaceuticals stock, see the EYPT Stock Forecast page.
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.
The most recent analyst rating on (EYPT) stock is a Buy with a $28.00 price target. To see the full list of analyst forecasts on EyePoint Pharmaceuticals stock, see the EYPT Stock Forecast page.
EyePoint Pharmaceuticals has recently completed a Phase 2 clinical study titled A Phase 2, Multicenter, Prospective, Double-masked, Parallel Study of EYP-1901, a Tyrosine Kinase Inhibitor (TKI), Compared to Sham for the Improvement of Moderately Severe to Severe Nonproliferative Diabetic Retinopathy (NPDR). The study aimed to evaluate the efficacy and safety of EYP-1901, a novel intravitreal drug, in improving the condition of patients with NPDR. This study is significant as it explores a potential new treatment option for diabetic retinopathy, a leading cause of blindness.
EyePoint Pharma’s recent earnings call painted a picture of strong operational execution and clinical progress, despite financial challenges. The company showcased rapid enrollment in pivotal trials and robust financial positioning, although it faced a decline in revenue and increased losses due to higher operating costs. This balance of positive clinical achievements and financial hurdles was a key theme throughout the call.
EyePoint Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company focused on developing and commercializing innovative treatments for serious retinal diseases, with its lead product candidate DURAVYU™ aimed at improving patient outcomes in conditions such as wet age-related macular degeneration (AMD) and diabetic macular edema (DME).
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.
The most recent analyst rating on (EYPT) stock is a Buy with a $30.00 price target. To see the full list of analyst forecasts on EyePoint Pharmaceuticals stock, see the EYPT Stock Forecast page.