Alector (ALEC)
:ALEC
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Alector (ALEC) AI Stock Analysis

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ALEC

Alector

(NASDAQ:ALEC)

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Neutral 45 (OpenAI - 4o)
Rating:45Neutral
Price Target:
$1.50
▲(11.94% Upside)
Alector's overall stock score reflects significant financial and technical challenges. The company's financial performance is weak, with ongoing losses and cash flow issues. Technical analysis indicates bearish momentum. While the earnings call provides some optimism with a strong cash position and clinical progress, these are offset by regulatory and diagnostic challenges. The valuation remains a concern due to negative earnings and lack of dividends.
Positive Factors
Strong Cash Position
Alector's robust cash reserves ensure operational stability and support strategic objectives, allowing continued investment in R&D and clinical trials.
Pipeline Advancements
Progress in clinical trials, such as AL101, indicates potential for future breakthroughs and marketable therapies, enhancing long-term growth prospects.
Proprietary Technology Platform
Alector's proprietary platform underpins its R&D efforts, offering a competitive edge in developing innovative treatments for neurodegenerative diseases.
Negative Factors
Regulatory Challenges
Regulatory hurdles can delay trial progress and increase costs, impacting the timeline for bringing new therapies to market and affecting long-term strategy.
Financial Instability
Ongoing financial challenges, including losses and debt reliance, threaten Alector's ability to sustain operations without external funding, impacting long-term viability.
Complexity in Diagnosing FTD
The complexity of diagnosing FTD complicates patient enrollment and trial success, potentially delaying the development of effective treatments and market entry.

Alector (ALEC) vs. SPDR S&P 500 ETF (SPY)

Alector Business Overview & Revenue Model

Company DescriptionAlector, Inc., a clinical stage biopharmaceutical company, develops therapies for the treatment of neurodegeneration diseases. Its products include AL001, a humanized recombinant monoclonal antibody, which is in Phase III clinical trial for the treatment of frontotemporal dementia, Alzheimer's, Parkinson's, and amyotrophic lateral sclerosis diseases; and AL101 that is in Phase I clinical trial for the treatment of neurodegenerative diseases, including Alzheimer's and Parkinson's diseases. The company also offers AL002, a product candidate that is in Phase II clinical trial for the treatment of Alzheimer's disease; and AL003, which is in Phase I clinical trial for the treatment of Alzheimer's disease. In addition, its products in development stage include AL044 that targets MS4A4A, a risk gene for Alzheimer's disease. Alector, Inc. has a collaboration agreement with Adimab, LLC for the research and development of antibodies; and a strategic collaboration agreement with GlaxoSmithKline plc for the development and commercialization of monoclonal antibodies, such as AL001 and AL101 to treat neurodegenerative diseases. The company was founded in 2013 and is headquartered in South San Francisco, California.
How the Company Makes MoneyAlector generates revenue primarily through the development and commercialization of its therapeutic products. This includes revenue from partnerships and collaborations with pharmaceutical companies, which may involve milestone payments and royalties on product sales. Additionally, the company may receive funding through grants, public and private investments, and potential licensing agreements. The successful advancement of its clinical programs into later stages, as well as the eventual market approval and sales of its therapies, are key contributors to its revenue streams.

Alector Earnings Call Summary

Earnings Call Date:Aug 07, 2025
(Q2-2025)
|
% Change Since: |
Next Earnings Date:Mar 03, 2026
Earnings Call Sentiment Neutral
The earnings call presented several positive developments, including strong financial health, upcoming trial data, and completion of enrollment for a key program. However, significant challenges remain, such as regulatory hurdles and the complexity of diagnosing and treating FTD. The balance of promising advancements and existing challenges suggests a cautiously optimistic outlook.
Q2-2025 Updates
Positive Updates
Upcoming INFRONT-3 Trial Data
Alector is anticipating top-line data from their Phase III INFRONT-3 trial of latozinemab by mid-Q4 2025. This trial is pivotal as it targets frontotemporal dementia due to the GRN gene mutation, a rare form of dementia with no approved therapy.
Strong Financial Position
The company closed the quarter with $307.3 million in cash, expected to provide runway into the second half of 2027. This financial strength supports their strategic objectives.
Completion of AL101 Phase II Enrollment
The enrollment for the Phase II trial of AL101 in early Alzheimer's disease was completed in April, with trial completion expected in 2026. AL101 aims to elevate progranulin levels, similar to latozinemab, for more prevalent neurodegenerative diseases.
Progranulin Elevation as a Key Endpoint
The FDA has recommended including plasma progranulin as a co-primary endpoint in the INFRONT-3 trial, highlighting its importance as a biologically meaningful marker in FTD-GRN.
Negative Updates
Regulatory Challenges
The FDA requested a change in the statistical analysis plan for the INFRONT-3 trial to include progranulin as a co-primary endpoint, which requires statistical significance on both co-primary endpoints for the study to be positive.
Complexity in Diagnosing Frontotemporal Dementia
FTD is frequently misdiagnosed or diagnosed late, with genetic testing not routinely performed. This complexity poses challenges in tailoring interventions and enrolling appropriate patients in clinical trials.
No Approved Treatments for FTD
Despite ongoing trials, there are currently no FDA-approved disease-modifying treatments for frontotemporal dementia, underscoring the urgent need for continued innovation.
Company Guidance
During the Alector Second Quarter and Midyear 2025 Earnings Conference Call, the company provided guidance on several key metrics. They reported a strong cash position of $307.3 million, which is expected to fund operations into the second half of 2027. For fiscal year 2025, Alector anticipates collaboration revenue to be between $13 million and $18 million, with total research and development expenses projected at $130 million to $140 million. General and administrative expenses are forecasted to range from $55 million to $65 million. The company is focused on advancing its late-stage clinical programs, particularly the Phase III INFRONT-3 trial for latozinemab, with pivotal data expected by mid-fourth quarter. They are also progressing the Phase II trial of AL101 for early Alzheimer's disease, with trial completion expected in 2026. Alector highlighted their proprietary technology platform, which supports their preclinical pipeline, including a brain-penetrant anti-amyloid beta antibody for Alzheimer's and an engineered GCase enzyme replacement therapy for Parkinson's disease.

Alector Financial Statement Overview

Summary
Alector's financial statements depict significant challenges in profitability, revenue growth, and cash flow management. The income statement shows consistent losses and declining revenue, while the balance sheet indicates reliance on debt financing. The cash flow statement highlights ongoing cash burn without significant improvement. Overall, the financial health is concerning, requiring strategic initiatives for long-term sustainability.
Income Statement
45
Neutral
Alector's income statement reveals consistent losses with declining revenue over recent years. The gross profit margin is volatile, indicating unstable cost management. The net profit margin is negative, reflecting ongoing unprofitability. Revenue growth rate is negative, highlighting shrinking sales. The company struggles with EBIT and EBITDA margins, displaying operating inefficiencies. Overall, Alector's income statement shows significant challenges in achieving profitability and revenue growth.
Balance Sheet
50
Neutral
Alector's balance sheet shows a relatively high debt-to-equity ratio, indicating reliance on debt financing. The return on equity is negative due to net losses, signaling challenges in generating shareholder value. The equity ratio is moderate, suggesting a balanced capital structure. However, the diminishing equity over time points to eroding financial strength. While the company maintains a reasonable level of assets, financial stability remains a concern.
Cash Flow
40
Negative
The cash flow statement highlights Alector's negative free cash flow growth rate, reflecting ongoing cash burn without significant improvement. The operating cash flow to net income ratio is negative, indicating insufficient cash generation from core operations. Free cash flow to net income ratio is also negative, underscoring inefficiencies in converting earnings into cash. Alector faces significant challenges in managing cash flows sustainably.
BreakdownTTMDec 2024Dec 2023Dec 2022Dec 2021Dec 2020
Income Statement
Total Revenue69.05M100.56M97.06M133.62M207.09M21.10M
Gross Profit22.59M100.56M88.21M133.62M17.68M-135.77M
EBITDA-112.36M-136.16M-142.89M-129.36M-29.05M-187.91M
Net Income-107.74M-119.05M-130.39M-133.31M-36.33M-190.23M
Balance Sheet
Total Assets335.29M468.30M621.83M787.65M814.66M488.25M
Cash, Cash Equivalents and Short-Term Investments291.11M413.40M548.86M712.85M735.25M413.31M
Total Debt37.88M42.52M38.92M43.33M47.60M51.26M
Total Liabilities277.57M341.50M487.67M573.21M513.93M220.72M
Stockholders Equity57.71M126.80M134.16M214.44M300.72M267.53M
Cash Flow
Free Cash Flow-197.58M-231.16M-186.54M-24.45M295.30M-171.77M
Operating Cash Flow-197.37M-229.91M-184.16M-20.33M298.55M-166.73M
Investing Cash Flow212.40M107.13M101.92M-159.01M-49.66M-105.05M
Financing Cash Flow24.61M81.54M2.55M4.51M30.30M232.11M

Alector Technical Analysis

Technical Analysis Sentiment
Negative
Last Price1.34
Price Trends
50DMA
2.52
Negative
100DMA
2.18
Negative
200DMA
1.78
Negative
Market Momentum
MACD
-0.38
Positive
RSI
29.26
Positive
STOCH
36.74
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For ALEC, the sentiment is Negative. The current price of 1.34 is below the 20-day moving average (MA) of 1.78, below the 50-day MA of 2.52, and below the 200-day MA of 1.78, indicating a bearish trend. The MACD of -0.38 indicates Positive momentum. The RSI at 29.26 is Positive, neither overbought nor oversold. The STOCH value of 36.74 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Negative sentiment for ALEC.

Alector Risk Analysis

Alector disclosed 79 risk factors in its most recent earnings report. Alector 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

Alector Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
54
Neutral
$331.46M-72.72%-89.01%-86.17%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
45
Neutral
$146.26M-121.98%12.26%37.36%
45
Neutral
-100.00%72.45%
41
Neutral
$199.55M-2.85-3.91%37.89%
33
Underperform
$128.61M-686.12%
33
Underperform
$451.83M-1.78-104.35%20.71%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
ALEC
Alector
1.34
-3.57
-72.71%
ACIU
AC Immune SA
3.28
-0.27
-7.61%
IMAB
I-MAB
4.00
2.93
273.83%
FHTX
Foghorn Therapeutics
4.53
-4.27
-48.52%
VOR
Vor Biopharma
10.06
-7.89
-43.96%
NMRA
Neumora Therapeutics, Inc.
2.86
-8.83
-75.53%

Alector Corporate Events

Alector’s Latozinemab Study: A Promising Continuation for Neurodegenerative Disease Treatment
Oct 27, 2025

Study Overview: Alector Inc. is conducting a continuation study titled ‘A Continuation Study of Latozinemab in Participants With Neurodegenerative Disease.’ The study aims to provide ongoing access to latozinemab for participants who have previously been involved in a latozinemab study, focusing on its potential benefits for neurodegenerative conditions.

Business Operations and StrategyExecutive/Board Changes
Alector Announces Major Workforce Reduction Post-Trial
Negative
Oct 21, 2025

On October 21, 2025, Alector announced a significant workforce reduction of approximately 49% to align with strategic priorities following the results of the Phase 3 INFRONT-3 clinical trial for latozinemab (AL001) in frontotemporal dementia, which did not meet its primary endpoint. The company is discontinuing the open-label extension and continuation study for latozinemab, impacting around 75 employees with restructuring charges estimated at $7.7 million. Additionally, Sara Kenkare-Mitra, President and Head of Research and Development, resigned effective December 22, 2025, to pursue other opportunities, with a separation agreement in place. Despite the trial’s outcome, Alector remains committed to advancing its pipeline, including ongoing collaborations and preclinical programs, supported by its proprietary ABC platform.

The most recent analyst rating on (ALEC) stock is a Buy with a $10.00 price target. To see the full list of analyst forecasts on Alector stock, see the ALEC Stock Forecast page.

Alector’s Earnings Call: Progress and Challenges in Neurodegenerative Treatments
Aug 13, 2025

Alector’s recent earnings call presented a mixed sentiment, highlighting notable progress in clinical trials and strategic collaborations, particularly with GSK, aimed at developing treatments for neurodegenerative diseases. Despite these advancements, the company faces ongoing challenges in addressing unmet needs in frontotemporal dementia (FTD) and navigating the complexities of regulatory requirements.

Alector Advances Neurodegenerative Therapies Amid Financial Updates
Aug 8, 2025

Alector is a late-stage clinical biotechnology company dedicated to developing therapies for neurodegenerative diseases, leveraging genetics, immunology, and neuroscience. The company is known for its innovative approach to addressing conditions such as frontotemporal dementia, Alzheimer’s disease, and Parkinson’s disease.

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 05, 2025