| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 1.02B | 781.37M | 396.59M | 75.42M | 66.56M | 250.65M |
| Gross Profit | 902.24M | 663.64M | 338.08M | 69.79M | 61.36M | 225.60M |
| EBITDA | 93.37M | -154.53M | -495.21M | -617.39M | -731.27M | -312.23M |
| Net Income | 44.99M | -197.88M | -528.63M | -652.17M | -746.35M | -344.87M |
Balance Sheet | ||||||
| Total Assets | 1.06B | 885.05M | 788.73M | 760.22M | 881.76M | 960.57M |
| Cash, Cash Equivalents and Short-Term Investments | 479.17M | 411.29M | 352.30M | 551.80M | 700.55M | 877.65M |
| Total Debt | 114.28M | 469.78M | 110.93M | 112.71M | 210.22M | 377.73M |
| Total Liabilities | 657.55M | 656.51M | 594.21M | 590.35M | 683.10M | 756.01M |
| Stockholders Equity | 401.17M | 228.54M | 194.52M | 169.87M | 198.66M | 204.56M |
Cash Flow | ||||||
| Free Cash Flow | 78.64M | -88.27M | -595.51M | -515.27M | -564.23M | -165.91M |
| Operating Cash Flow | 78.86M | -87.87M | -594.74M | -513.75M | -563.13M | -160.49M |
| Investing Cash Flow | -225.00K | -403.00K | -674.00K | 59.89M | 247.62M | -316.99M |
| Financing Cash Flow | 3.63M | 149.24M | 394.50M | 365.66M | 392.24M | 692.18M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
60 Neutral | $4.36B | ― | -31.14% | ― | ― | -11.39% | |
58 Neutral | $4.01B | ― | -36.94% | ― | ― | -9.10% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | $2.49B | 64.87 | 14.10% | ― | 42.11% | ― | |
51 Neutral | $3.60B | ― | -15.81% | ― | 53.66% | 58.63% | |
45 Neutral | $2.86B | ― | -28.39% | ― | 32.38% | 33.47% | |
41 Neutral | $678.05M | ― | -54.17% | ― | ― | -157.74% |
The recent earnings call of Apellis Pharmaceuticals highlighted a blend of significant achievements and notable challenges. The company celebrated the FDA approval of EMPAVELI and the strong market leadership of SYFOVRE. However, there were concerns regarding SYFOVRE’s revenue, which was impacted by free drug programs and operational challenges in patient access.
Apellis Pharmaceuticals, Inc. is a commercial-stage biopharmaceutical company focused on developing novel therapeutic compounds that target the complement system, particularly at the C3 protein level, to treat diseases with high unmet needs. The company is headquartered in Waltham, Massachusetts, and is known for its products EMPAVELI and SYFOVRE, which are used to treat conditions such as paroxysmal nocturnal hemoglobinuria and geographic atrophy secondary to age-related macular degeneration, respectively.
Apellis Pharmaceuticals is conducting a Phase 2 clinical study titled A Phase 2, Randomized, Placebo Controlled, Multicenter, Masked Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacodynamics of Multidose APL 3007 in Combination With Syfovre/Pegcetacoplan (APL-2) in Patients Diagnosed With Geographic Atrophy Secondary to Age Related Macular Degeneration. The study aims to assess the effectiveness and safety of APL-3007, in combination with Syfovre/Pegcetacoplan, for treating geographic atrophy due to age-related macular degeneration, a significant cause of vision loss.
Apellis Pharmaceuticals is conducting a Phase 3B, single-arm, open-label study titled A Phase 3B, Single-Arm, Open-Label, Multicenter Study to Evaluate the Safety of Pegcetacoplan in a Prefilled Syringe in Participants With Geographic Atrophy Secondary to Age-Related Macular Degeneration. The study aims to assess the safety of pegcetacoplan, a complement C3 inhibitor, in a prefilled syringe for treating geographic atrophy secondary to age-related macular degeneration.
Apellis Pharmaceuticals is conducting a sequential Phase 2/3 study titled ‘A Sequential Phase 2/3 Study of APL2 in Patients With Focal Segmental Glomerulosclerosis.’ The study aims to evaluate the efficacy and safety of APL2, a complement (C3) inhibitor, in treating Focal Segmental Glomerulosclerosis (FSGS), a rare kidney disease. This study is significant as it could offer a new treatment option for patients with limited alternatives.
Apellis Pharmaceuticals is conducting a study titled An Open Label, Single-Arm, Phase 2 Study to Evaluate the Safety, Pharmacokinetics, and Biologic Activity of Pegcetacoplan in Pediatric Patients With Paroxysmal Nocturnal Hemoglobinuria. The study aims to assess the safety and effectiveness of pegcetacoplan in adolescents aged 12-17 with paroxysmal nocturnal hemoglobinuria (PNH), a rare blood disorder. This research is significant as it targets a younger demographic, potentially expanding treatment options for this condition.
Apellis Pharmaceuticals is conducting a Phase 3 study titled ‘A Phase 3 Study to Evaluate the Efficacy and Safety of Pegcetacoplan in Adults at High Risk of Delayed Graft Function (DGF) Following Kidney Allograft Transplantation.’ The study aims to assess the effectiveness and safety of Pegcetacoplan, a complement (C3) inhibitor, in preventing delayed graft function in patients undergoing kidney transplants. This research is significant as it could improve outcomes for patients with end-stage renal disease receiving deceased donor kidney transplants.
Apellis Pharmaceuticals is conducting a phase 4 clinical study titled ‘A Prospective, Multicenter, Open-Label, Observational Phase 4 Study to Evaluate Real-World Safety, Tolerability, and Treatment Patterns of Pegcetacoplan (Syfovre) in Patients With Geographic Atrophy Secondary to Age-Related Macular Degeneration.’ The study aims to assess the real-world safety and treatment patterns of Pegcetacoplan in patients with geographic atrophy, a condition associated with age-related macular degeneration.