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Apellis Pharmaceuticals (APLS)
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Apellis Pharmaceuticals (APLS) AI Stock Analysis

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APLS

Apellis Pharmaceuticals

(NASDAQ:APLS)

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Neutral 51 (OpenAI - 4o)
Rating:51Neutral
Price Target:
$19.50
▲(1.25% Upside)
The overall stock score of 51 reflects a mixed outlook for Apellis Pharmaceuticals. The most significant factor is the company's financial performance, showing improvement in cash flow and leverage but facing challenges in revenue growth. Technical analysis indicates bearish momentum, while valuation suggests the stock may be overvalued. The earnings call provided positive insights into strategic initiatives and FDA approvals, but revenue challenges remain a concern.
Positive Factors
FDA Approval of EMPAVELI
The FDA approval of EMPAVELI expands Apellis's market, potentially increasing revenue and strengthening its position in the nephrology sector.
Strong Financial Position
A robust cash position allows Apellis to invest in R&D and strategic initiatives, supporting sustainable growth and innovation.
SYFOVRE Market Leadership
SYFOVRE's market leadership in geographic atrophy provides a stable revenue stream and reinforces Apellis's competitive advantage.
Negative Factors
Challenges with SYFOVRE Revenue
Revenue challenges from free drug programs could impact profitability and hinder the ability to reinvest in growth opportunities.
Low Treatment Rate for Geographic Atrophy
The low treatment rate for geographic atrophy limits market penetration and revenue potential for Apellis's therapies.
Operational Challenges in Patient Access
Patient access issues could limit therapy adoption, affecting revenue growth and market expansion efforts for Apellis.

Apellis Pharmaceuticals (APLS) vs. SPDR S&P 500 ETF (SPY)

Apellis Pharmaceuticals Business Overview & Revenue Model

Company DescriptionApellis Pharmaceuticals, Inc. is a biopharmaceutical company focused on developing innovative therapies to treat serious diseases. The company specializes in complement immunotherapy, targeting the complement system to provide solutions for conditions such as geographic atrophy and other rare diseases. Apellis is primarily engaged in the research, development, and commercialization of its core product, pegcetacoplan, which is designed to address unmet medical needs in the ophthalmology and hematology sectors.
How the Company Makes MoneyApellis Pharmaceuticals generates revenue primarily through the sale of its approved therapies, notably pegcetacoplan, which is marketed for the treatment of geographic atrophy, a complication of age-related macular degeneration. The company's revenue model is based on a combination of product sales, potential royalties from partnerships, and collaborations with other pharmaceutical companies. Significant partnerships with larger pharmaceutical firms enhance its research capabilities and market reach, contributing to Apellis's earnings. Additionally, the company may receive milestone payments from partners based on the achievement of specific development and commercial milestones.

Apellis Pharmaceuticals Key Performance Indicators (KPIs)

Any
Any
Product Revenue by Segment
Product Revenue by Segment
Highlights revenue from different product lines, providing insight into which segments are driving growth and how diversified the company's income streams are.
Chart InsightsApellis Pharmaceuticals' SYFOVRE segment is driving growth with a strong market position, despite revenue impacts from high free goods usage. EMPAVELI's revenue saw a modest increase, supported by recent FDA approvals. The company's strategic moves, including a significant cash infusion from Sobi, bolster financial stability. However, challenges with co-pay assistance and flat commercial vial growth for SYFOVRE highlight potential revenue constraints. Management remains optimistic about achieving sustainable profitability, leveraging their robust cash position and market leadership in geographic atrophy.
Data provided by:Main Street Data

Apellis Pharmaceuticals Earnings Call Summary

Earnings Call Date:Oct 30, 2025
(Q3-2025)
|
% Change Since: |
Next Earnings Date:Mar 04, 2026
Earnings Call Sentiment Neutral
The earnings call reflected significant progress with the FDA approval of EMPAVELI and strong market leadership of SYFOVRE. However, challenges in SYFOVRE revenue due to free drug programs and operational challenges in patient access were notable concerns.
Q3-2025 Updates
Positive Updates
FDA Approval of EMPAVELI
EMPAVELI was approved for treating patients 12 years and older with C3 glomerulopathy (C3G) or primary immune complex membranoproliferative glomerulonephritis (IC-MPGN), expanding the addressable market by approximately 5,000 patients.
SYFOVRE Market Leadership
SYFOVRE maintained its leading position, accounting for an estimated 52% of new patient starts and more than 60% of the overall market.
Strong Financial Performance
Total revenue for the third quarter was $459 million, including a $275 million upfront payment from Sobi.
Positive EMPAVELI Launch Feedback
The market feedback for EMPAVELI has been exceptionally positive, highlighting its ease of use and the convenience of twice-weekly dosing.
Continued Injection Growth for SYFOVRE
SYFOVRE experienced a 4% growth in total estimated injections during the quarter.
Negative Updates
Challenges with SYFOVRE Revenue
SYFOVRE revenue faced a $15 million headwind due to elevated use of free goods, slightly higher than expected.
Low Treatment Rate for Geographic Atrophy
Only about 10% of patients diagnosed with geographic atrophy are currently treated with complement inhibitors.
Headwinds from Free Drug Programs
Free drug programs have been a nearly $40 million headwind to SYFOVRE revenue through the first three quarters.
Operational Challenges in Patient Access
Operational challenges related to patient access and co-pay assistance have been significant headwinds affecting market growth.
Company Guidance
During the Apellis Pharmaceuticals Third Quarter 2025 Earnings Conference Call, the company provided guidance indicating significant progress and strategic initiatives to drive future growth. The key highlight was the FDA approval of EMPAVELI for C3 glomerulopathy and IC-MPGN, expanding its market by approximately 5,000 patients. This approval is expected to deliver meaningful results across proteinuria reduction, eGFR stabilization, and substantial C3 deposit clearance. Apellis is also preparing to launch EMPAVELI with a target of 225 cumulative patient start forms by the end of the year and has scaled its field teams to 100 people to cover U.S. nephrologists. For SYFOVRE, which has demonstrated a 4% injection growth this quarter, the company anticipates steady growth driven by new tools and market education initiatives over the next 12 to 18 months. Financially, total revenue for the quarter was $459 million, including $151 million from SYFOVRE and $27 million from EMPAVELI across all indications, with a noted $15 million revenue headwind from free goods. Apellis remains confident in its long-term market strategy and the transformative impact of its therapies, supported by a strong cash position of $475 million, allowing for further pipeline advancements.

Apellis Pharmaceuticals Financial Statement Overview

Summary
Apellis Pharmaceuticals shows improvement in cash flow and leverage, with a strong recovery in free cash flow and reduced debt-to-equity ratio. However, challenges remain in maintaining consistent revenue growth and profitability, as evidenced by historical volatility and a slight decline in revenue.
Income Statement
45
Neutral
Apellis Pharmaceuticals shows a mixed performance in its income statement. The TTM data indicates a gross profit margin of 84.53%, which is strong, but the net profit margin is relatively low at 6.12%. Revenue has slightly declined by 2.53% in the TTM period, indicating potential challenges in maintaining growth. EBIT and EBITDA margins are positive in the TTM, showing improvement from previous years, but historical data shows significant losses, highlighting volatility in profitability.
Balance Sheet
50
Neutral
The balance sheet reflects a moderate financial position. The debt-to-equity ratio has improved significantly to 0.28 in the TTM, indicating reduced leverage compared to previous years. Return on equity is positive at 18.94%, showing effective use of equity to generate profits. However, historical high leverage and negative ROE in previous years suggest past financial instability.
Cash Flow
60
Neutral
Cash flow analysis reveals a strong recovery in free cash flow, with a growth rate of 1681.56% in the TTM. The operating cash flow to net income ratio is 0.28, indicating some efficiency in converting income to cash. The free cash flow to net income ratio is nearly 1, suggesting that the company is generating cash flow in line with its net income, a positive sign for liquidity.
BreakdownTTMDec 2024Dec 2023Dec 2022Dec 2021Dec 2020
Income Statement
Total Revenue1.02B781.37M396.59M75.42M66.56M250.65M
Gross Profit902.24M663.64M338.08M69.79M61.36M225.60M
EBITDA93.37M-154.53M-495.21M-617.39M-731.27M-312.23M
Net Income44.99M-197.88M-528.63M-652.17M-746.35M-344.87M
Balance Sheet
Total Assets1.06B885.05M788.73M760.22M881.76M960.57M
Cash, Cash Equivalents and Short-Term Investments479.17M411.29M352.30M551.80M700.55M877.65M
Total Debt114.28M469.78M110.93M112.71M210.22M377.73M
Total Liabilities657.55M656.51M594.21M590.35M683.10M756.01M
Stockholders Equity401.17M228.54M194.52M169.87M198.66M204.56M
Cash Flow
Free Cash Flow78.64M-88.27M-595.51M-515.27M-564.23M-165.91M
Operating Cash Flow78.86M-87.87M-594.74M-513.75M-563.13M-160.49M
Investing Cash Flow-225.00K-403.00K-674.00K59.89M247.62M-316.99M
Financing Cash Flow3.63M149.24M394.50M365.66M392.24M692.18M

Apellis Pharmaceuticals Technical Analysis

Technical Analysis Sentiment
Negative
Last Price19.26
Price Trends
50DMA
24.73
Negative
100DMA
23.25
Negative
200DMA
22.77
Negative
Market Momentum
MACD
-1.34
Positive
RSI
32.55
Neutral
STOCH
4.88
Positive
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For APLS, the sentiment is Negative. The current price of 19.26 is below the 20-day moving average (MA) of 24.68, below the 50-day MA of 24.73, and below the 200-day MA of 22.77, indicating a bearish trend. The MACD of -1.34 indicates Positive momentum. The RSI at 32.55 is Neutral, neither overbought nor oversold. The STOCH value of 4.88 is Positive, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Negative sentiment for APLS.

Apellis Pharmaceuticals Risk Analysis

Apellis Pharmaceuticals disclosed 75 risk factors in its most recent earnings report. Apellis Pharmaceuticals reported the most risks in the "Tech & Innovation" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Apellis Pharmaceuticals Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
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
$2.49B64.8714.10%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%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
APLS
Apellis Pharmaceuticals
19.26
-10.72
-35.76%
ZLAB
Zai Lab
21.90
-8.72
-28.48%
CRNX
Crinetics Pharmaceuticals
40.00
-20.69
-34.09%
AKRO
Akero Therapeutics
54.04
19.59
56.87%
MIRM
Mirum Pharmaceuticals
68.11
26.11
62.17%
MLTX
MoonLake Immunotherapeutics
10.63
-41.15
-79.47%

Apellis Pharmaceuticals Corporate Events

Apellis Pharmaceuticals’ Earnings Call Highlights FDA Approval and Market Challenges
Nov 1, 2025

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 Reports Strong Q3 2025 Earnings
Oct 31, 2025

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’ Promising Phase 2 Study on Geographic Atrophy Treatment
Oct 27, 2025

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 Launches Phase 3B Study for Pegcetacoplan in Geographic Atrophy
Oct 27, 2025

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 Advances APL2 Study for Rare Kidney Disease
Oct 27, 2025

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 Advances Pediatric PNH Treatment Study
Oct 27, 2025

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’ Phase 3 Study on Pegcetacoplan: A Potential Game-Changer for Kidney Transplants
Oct 27, 2025

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’ Phase 4 Study Update: Real-World Insights on Pegcetacoplan
Oct 27, 2025

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.

Glossary
BuyA stock rated as a "Buy" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock is likely to deliver higher returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
HoldA stock rated as a "Hold" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly compelling nor unfavorable for investment. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
SellA stock rated as a "Sell" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock may deliver lower returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.

Disclaimer

This AI Analyst Stock Report is automatically generated by our AI systems using advanced algorithms and publicly available financial, technical, and market data. While the information provided aims to be accurate and insightful, it is intended for informational purposes only and should not be considered financial advice. Any content created by an AI (Artificial Intelligence) system may contain inaccuracies and/or contain errors. Investing in stocks carries inherent risks, and past performance is not indicative of future results. This report does not account for your personal financial circumstances, objectives, or risk tolerance. Always conduct your own research or consult with a qualified financial advisor before making investment decisions. The analysis and recommendations provided are based on historical and current data and may not fully reflect future market conditions or unexpected developments. Neither the creators of this report nor its affiliated entities guarantee the accuracy, completeness, or reliability of the information presented. Use this report at your own discretion and risk.Date of analysis: Nov 08, 2025