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Beam Therapeutics (BEAM)
NASDAQ:BEAM
US Market

Beam Therapeutics (BEAM) AI Stock Analysis

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Beam Therapeutics

(NASDAQ:BEAM)

39Underperform
Beam Therapeutics faces considerable financial and technical challenges, reflected in its negative profitability and bearish stock trend. While recent positive trial data and advancements in base editing are promising, these factors are not sufficient to offset the financial and technical weaknesses currently impacting the stock.
Positive Factors
Clinical Trials
Impressive early results for BEAM-302 show a promising effect in correcting the disease-causing PiZ mutation in patients with alpha-1 antitrypsin deficiency (AATD).
Financial Position
The $1.35 billion cash position provides Beam Therapeutics with a strong financial runway into 2028, sufficient to advance current therapies into late-stage studies.
Negative Factors
Market Sentiment
Investors seem to be imposing a higher bar than clinicians.
Regulatory Challenges
Regulatory: Highly uncertain. Dr. Rennard thinks it may be 'overly optimistic' to think FDA will apply the 11 micromolar approval bar to novel modalities.

Beam Therapeutics (BEAM) vs. S&P 500 (SPY)

Beam Therapeutics Business Overview & Revenue Model

Company DescriptionBeam Therapeutics Inc., a biotechnology company, develops precision genetic medicines for patients suffering from serious diseases in the United States. The company is developing BEAM-101 for the treatment of sickle cell disease and beta thalassemia; BEAM-102 for the treatment of sickle cell disease; and BEAM-201, an allogeneic chimeric antigen receptor T cell for the treatment of relapsed/refractory T-cell acute lymphoblastic leukemia; and BEAM-301, a liver-targeted development candidate for the treatment of patients with Glycogen Storage Disease Type Ia. It also develops therapies for alpha-1 antitrypsin deficiency; ocular diseases; and other liver, muscle, and central nervous system disorders. The company has an alliance with Boston Children's Hospital; a research and clinical trial collaboration agreement with Magenta Therapeutics, Inc.; license agreement with Sana Biotechnology, Inc.; and a research collaboration with the Institute of Molecular and Clinical Ophthalmology Basel. It also has a research collaboration agreement with Pfizer Inc. and Apellis Pharmaceuticals, Inc.; and collaboration and license agreement with Verve Therapeutics, Inc. The company was incorporated in 2017 and is based in Cambridge, Massachusetts.
How the Company Makes MoneyBeam Therapeutics primarily makes money through the advancement and commercialization of its therapeutic candidates. The company generates revenue by entering into strategic collaborations and partnerships with other pharmaceutical and biotechnology companies, which may include upfront payments, milestone payments, and royalties based on the successful development and commercialization of its therapies. Additionally, Beam may generate revenue through grants and research funding from government or private institutions. As the company progresses its pipeline, future revenue could also come from the direct sale of its approved therapies.

Beam Therapeutics Financial Statement Overview

Summary
Beam Therapeutics faces significant financial challenges with negative profitability and cash flow metrics. Revenue volatility and consistent net losses pose concerns for long-term sustainability. Despite a strong equity position, the inability to generate positive operating cash flow and profitability could hinder future growth and strategic investments.
Income Statement
35
Negative
Beam Therapeutics has experienced significant revenue fluctuations with revenue dropping to zero in 2024 from $377.7 million in 2023. Gross profit margins have been negative, indicating costs are exceeding revenues. Net profit margins are also negative, with substantial net losses reported each year, highlighting profitability challenges. EBIT and EBITDA margins are deeply negative, illustrating operating inefficiencies and high expense relative to revenue.
Balance Sheet
55
Neutral
The company maintains a strong equity position with a debt-to-equity ratio of 0.22 in 2024, indicating moderate financial leverage. However, the return on equity is negative due to consistent net losses, reflecting inefficiencies in generating shareholder value. The equity ratio remains stable, showing substantial reliance on equity financing. Cash reserves are strong, which provides financial stability despite operational losses.
Cash Flow
40
Negative
Cash flow analysis indicates challenges with operating cash flow being zero in 2024, down from a negative position in previous years, impacting liquidity. Free cash flow remains negative, showing the company is not generating sufficient cash to cover its capital expenditures. The lack of positive cash flow from operations compared to net income suggests difficulty in converting revenue into cash.
Breakdown
Dec 2024Dec 2023Dec 2022Dec 2021Dec 2020
Income StatementTotal Revenue
63.52M377.71M60.92M51.84M24.00K
Gross Profit
63.52M-59.67M38.34M35.40M-103.16M
EBIT
-415.57M-176.49M-338.48M-392.46M-132.76M
EBITDA
-415.57M-156.47M-324.33M-392.46M-128.03M
Net Income Common Stockholders
-376.74M-132.53M-263.59M-341.36M-256.42M
Balance SheetCash, Cash Equivalents and Short-Term Investments
850.74M1.19B1.08B965.65M299.67M
Total Assets
1.10B1.46B1.34B1.47B451.68M
Total Debt
161.43M172.69M179.00M142.35M100.23M
Net Debt
-120.54M-263.21M-53.76M-823.30M-61.94M
Total Liabilities
370.28M478.38M608.24M647.72M206.12M
Stockholders Equity
733.54M981.33M733.47M826.74M245.56M
Cash FlowFree Cash Flow
-356.19M-182.93M-26.42M-113.08M-112.10M
Operating Cash Flow
-347.25M-149.19M22.53M-66.27M-95.74M
Investing Cash Flow
185.01M71.84M-461.34M-294.14M-100.12M
Financing Cash Flow
7.74M276.45M111.59M756.14M322.32M

Beam Therapeutics Technical Analysis

Technical Analysis Sentiment
Negative
Last Price14.63
Price Trends
50DMA
24.65
Negative
100DMA
25.47
Negative
200DMA
25.38
Negative
Market Momentum
MACD
-1.92
Positive
RSI
27.85
Positive
STOCH
13.95
Positive
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For BEAM, the sentiment is Negative. The current price of 14.63 is below the 20-day moving average (MA) of 19.71, below the 50-day MA of 24.65, and below the 200-day MA of 25.38, indicating a bearish trend. The MACD of -1.92 indicates Positive momentum. The RSI at 27.85 is Positive, neither overbought nor oversold. The STOCH value of 13.95 is Positive, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Negative sentiment for BEAM.

Beam Therapeutics Risk Analysis

Beam Therapeutics disclosed 85 risk factors in its most recent earnings report. Beam Therapeutics 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

Beam Therapeutics Peers Comparison

Overall Rating
UnderperformOutperform
Sector (48)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
48
Neutral
$6.36B1.28-45.04%2.64%19.24%1.69%
47
Neutral
$308.49M181.41%8001.47%-37.69%
41
Neutral
$732.90M-54.00%59.55%3.09%
39
Underperform
$1.63B-43.94%-83.18%-144.95%
37
Underperform
$2.53B-74.17%-43.10%
35
Underperform
$808.75M-78.34%-70.45%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
BEAM
Beam Therapeutics
14.63
-11.30
-43.58%
NTLA
Intellia Therapeutics
6.77
-17.50
-72.11%
PHAT
Phathom Pharmaceuticals
4.11
-6.03
-59.47%
ETNB
89bio
5.00
-4.82
-49.08%
IMVT
Immunovant
14.68
-14.67
-49.98%

Beam Therapeutics Earnings Call Summary

Earnings Call Date: Feb 25, 2025 | % Change Since: -52.48% | Next Earnings Date: May 13, 2025
Earnings Call Sentiment Neutral
The earnings call presented a mix of significant advancements in Beam's clinical programs, particularly in sickle cell disease and liver genetic diseases, alongside notable challenges related to patient safety in ongoing trials. While the progress in clinical data and technology development is promising, the safety concerns related to conditioning agents are a critical issue.
Highlights
Advancements in Sickle Cell Disease Treatment
Beam Therapeutics reported initial clinical data from the BEACON trial for BEAM-101, showing a significant increase in fetal hemoglobin (HbF) and a reduction in sickle hemoglobin (HbS) in patients with sickle cell disease. Patients achieved greater than 60% HbF, reducing HbS to less than 40%, which is consistent with sickle cell trait profiles.
Progress in Liver Genetic Disease Program
Beam-302, aimed at treating alpha-1 antitrypsin deficiency (AATD), has dosed its first patient, with plans to report initial data in 2025. This program intends to address both lung and liver manifestations of the disease.
ESCAPE Technology Development
Beam has nominated development candidates for ESCAPE technology, aiming to eliminate chemotherapy in transplants. Early nonhuman primate studies show promising engraftment and HbF induction without chemotherapy.
Strong Financial Position
Beam Therapeutics reported a strong financial position, supporting ongoing and future clinical development programs.
Lowlights
Patient Death in BEACON Trial
A patient in the BEACON trial died due to respiratory failure, likely related to busulfan conditioning. This highlights the risks associated with myeloablative conditioning in gene therapy.
Potential Safety Concerns with Conditioning
The use of busulfan in the BEACON trial has raised safety concerns, with known risks including lung injury and respiratory failure. This underscores the need for safer conditioning methods.
Company Guidance
In the Q3 2024 earnings call, Beam Therapeutics provided comprehensive updates on its clinical programs, highlighting significant progress and future expectations. The company reported that 35 patients have been enrolled in the BEACON trial for BEAM-101, with 8 patients already treated. The trial evaluates BEAM-101 for sickle cell disease, aiming for a best-in-class profile through efficient editing and induction of fetal hemoglobin (HbF) to over 60%, significantly reducing sickle hemoglobin (HbS) levels. Beam also shared promising preclinical data for its ESCAPE technology, which aims to eliminate the use of chemotherapy in stem cell transplants, potentially expanding the patient population up to fourfold. Additionally, Beam announced the completion of dosing in the first cohort of its BEAM-302 program for alpha-1 antitrypsin deficiency (AATD) and expects to report initial data in 2025. Financially, the company remains strong, supporting the continued development and potential commercialization of its pipeline.

Beam Therapeutics Corporate Events

Product-Related AnnouncementsBusiness Operations and Strategy
Beam Therapeutics Reports Positive Phase 1/2 Trial Data
Positive
Mar 10, 2025

On March 10, 2025, Beam Therapeutics announced positive initial data from its Phase 1/2 trial of BEAM-302 for treating alpha-1 antitrypsin deficiency (AATD). The trial demonstrated that BEAM-302, a liver-targeting lipid-nanoparticle formulation, was well tolerated and showed dose-dependent increases in functional AAT levels and decreases in mutant Z-AAT levels. This marks the first clinical genetic correction of a disease-causing mutation, offering potential treatment for both lung and liver disease in AATD patients. The company plans further dose escalation and expects to present more data in the second half of 2025.

Product-Related AnnouncementsBusiness Operations and Strategy
Beam Therapeutics Advances Base Editing Portfolio
Positive
Jan 13, 2025

Beam Therapeutics announced advancements in its base editing portfolio with key milestones anticipated in 2025. This progress is expected to bolster its industry positioning by advancing clinical programs, which aim to deliver life-long, curative genetic medicines, potentially impacting stakeholders through enhanced therapeutic options and financial stability.

Glossary
OutperformA stock rated as "Outperform" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests that the stock is likely to deliver higher returns compared to the average returns of other stocks in the same sector or market index. Investors might consider this stock a good buying opportunity.
NeutralA stock rated as "Neutral" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly attractive nor unattractive for investment. Investors may consider holding onto the stock, as it is not expected to either significantly outperform or underperform the market.
UnderperformA stock rated as "Underperform" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests that the stock may deliver lower returns compared to the average returns of other stocks in the same sector or market index. Investors might consider selling the stock or avoiding it as an investment.

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.