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Silence Therapeutics (SLN)
NASDAQ:SLN

Silence Therapeutics (SLN) AI Stock Analysis

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Silence Therapeutics

(NASDAQ:SLN)

47Neutral
Silence Therapeutics faces significant financial challenges with negative equity and cash flow issues despite revenue growth. Technical indicators are bearish, suggesting potential downside risk. The valuation is hindered by lack of profitability, though the company's strategic planning and extended cash runway offer some optimism. Earnings call highlights positive clinical progress but also strategic delays, impacting the overall score.
Positive Factors
Commercial opportunity
Zerlasiran's ~100% Lp(a) reduction in clinic, coupled with low dosing frequency and clean safety profile can render a significant commercial opportunity.
Financial flexibility
Silence's cash runway now extends into 2027, providing financial flexibility to advance its RNAi pipeline in rare diseases.
Regulatory validation
Zerlasiran represents a potential blockbuster opportunity, particularly with regulatory validation from the FDA (U.S.), EMA (Europe), and PMDA (Japan) on the pivotal trial design.
Negative Factors
Partnership delay
The PhIII start for the Lp(a) program is now paused until a partner is secured.
Stock weakness
The lack of a clear registrational trial design and the delay of a competitor catalyst from NVS/IONS have contributed to the stock weakness.

Silence Therapeutics (SLN) vs. S&P 500 (SPY)

Silence Therapeutics Business Overview & Revenue Model

Company DescriptionSilence Therapeutics plc, a biotechnology company, focuses on the discovery and development of novel ribonucleic acid (RNA) therapeutics in hematology, cardiovascular, and other rare and metabolic indications. The company's platform includes mRNAi GalNAc Oligonucleotide Discovery platform designed to accurately target specific disease-associated genes in the liver. It designs short interfering RNA molecules to harness the body's natural mechanism of RNA interference, and degrading messenger RNA molecules that encode specific targeted disease-associated proteins in a cell. The company is developing various product candidates, including SLN360, which is Phase I clinical trials for the treatment of cardiovascular disease with high lipoprotein; SLN124 that is in Phase I clinical trials for the treatment of non-transfusion dependent thalassemia, and Phase I clinical trials for the treatment of myelodysplastic syndrome; and SLN124 for the treatment of polycythemia vera. It has collaboration agreements with AstraZeneca PLC to discover, develop, and commercialize small interfering RNA therapeutics for the treatment of cardiovascular, renal, metabolic, and respiratory diseases; and Mallinckrodt Pharma IP Trading DAC to develop and commercialize RNAi drug targets designed to silence the complement cascade in complement-mediated disorders. The company also has a collaboration with Hansoh Pharmaceutical Group Company Limited to develop siRNAs for three undisclosed targets leveraging Silence's mRNAi GOLD platform. The company was formerly known as SR Pharma plc and changed its name to Silence Therapeutics plc in May 2007. Silence Therapeutics plc is headquartered in London, the United Kingdom.
How the Company Makes MoneySilence Therapeutics generates revenue primarily through collaborative agreements, licensing deals, and milestone payments associated with its RNAi platform. The company partners with pharmaceutical and biotechnology firms to co-develop therapies, leveraging its expertise in RNA interference technology. These partnerships often involve upfront payments, research funding, and potential milestone and royalty payments contingent upon the successful development and commercialization of new therapies. Additionally, Silence Therapeutics may receive revenue from licensing its technology to third parties, enabling them to use its RNAi platform for their own therapeutic developments.

Silence Therapeutics Financial Statement Overview

Summary
Silence Therapeutics is experiencing revenue growth, but profitability challenges persist due to negative EBIT and net income margins. The negative stockholders' equity and high liabilities signal financial instability, although substantial cash reserves provide some comfort. The negative free cash flow highlights ongoing cash challenges, despite the ability to secure financing.
Income Statement
45
Neutral
Silence Therapeutics has demonstrated significant revenue growth over the years, with a notable increase from 2023 to 2024. However, the company continues to face challenges with profitability, as evidenced by negative EBIT and net income margins. The consistent negative profit margins highlight a need for enhanced cost management or increased revenue to achieve profitability.
Balance Sheet
30
Negative
The company's balance sheet reveals a concerning negative stockholders' equity as of 2024, indicating financial instability. The debt-to-equity ratio is not favorable due to the negative equity, and although the company maintains substantial cash reserves, the high liabilities present a risk. Improving equity and managing liabilities are critical for financial health.
Cash Flow
55
Neutral
Silence Therapeutics has managed significant financing cash flow, which supports its operations despite negative operating cash flow. The free cash flow has been consistently negative, reflecting ongoing cash challenges. However, the company's ability to secure financing offers some operational flexibility. Improving free cash flow is essential for sustainable growth.
Breakdown
Dec 2024Dec 2023Dec 2022Dec 2021Dec 2020
Income StatementTotal Revenue
43.26M25.38M17.50M12.41M5.48M
Gross Profit
31.45M15.06M6.62M4.96M1.72M
EBIT
-63.32M-49.60M-48.59M-45.81M-35.85M
EBITDA
-48.99M-49.78M-47.88M-45.42M-35.53M
Net Income Common Stockholders
-45.31M-43.27M-40.49M-39.41M-32.55M
Balance SheetCash, Cash Equivalents and Short-Term Investments
147.33M54.03M71.14M73.54M37.45M
Total Assets
202.63M93.82M107.50M96.19M85.97M
Total Debt
117.00K272.00K446.00K137.00K341.00K
Net Debt
-121.21M-53.76M-54.37M-73.40M-27.11M
Total Liabilities
68.61M76.77M85.43M87.67M76.91M
Stockholders Equity
-134.02M17.05M22.07M8.53M9.06M
Cash FlowFree Cash Flow
-67.85M-39.40M-45.90M5.47M-11.29M
Operating Cash Flow
-67.64M-39.35M-45.46M6.81M-10.78M
Investing Cash Flow
-21.97M16.43M-16.54M8.68M9.62M
Financing Cash Flow
142.09M25.16M43.05M30.71M15.43M

Silence Therapeutics Technical Analysis

Technical Analysis Sentiment
Negative
Last Price3.62
Price Trends
50DMA
4.77
Negative
100DMA
7.35
Negative
200DMA
13.06
Negative
Market Momentum
MACD
-0.40
Positive
RSI
32.01
Neutral
STOCH
14.72
Positive
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For SLN, the sentiment is Negative. The current price of 3.62 is below the 20-day moving average (MA) of 4.19, below the 50-day MA of 4.77, and below the 200-day MA of 13.06, indicating a bearish trend. The MACD of -0.40 indicates Positive momentum. The RSI at 32.01 is Neutral, neither overbought nor oversold. The STOCH value of 14.72 is Positive, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Negative sentiment for SLN.

Silence Therapeutics Risk Analysis

Silence Therapeutics disclosed 70 risk factors in its most recent earnings report. Silence Therapeutics reported the most risks in the “Finance & Corporate” category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Silence Therapeutics Peers Comparison

Overall Rating
UnderperformOutperform
Sector (49)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
PFPFE
68
Neutral
$144.91B18.559.05%6.46%8.77%272.80%
67
Neutral
$7.41B32.0219.71%52.97%
59
Neutral
$36.86B-414.62%22.97%38.54%
49
Neutral
$6.90B0.78-53.24%2.46%20.86%1.26%
48
Neutral
$13.06B-28.77%-52.75%25.00%
SLSLN
47
Neutral
$162.84M-99.23%-40.10%-16.60%
47
Neutral
$2.03B-600.68%-98.62%-86.21%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
SLN
Silence Therapeutics
3.62
-17.97
-83.23%
ALNY
Alnylam Pharma
280.96
128.99
84.88%
ARWR
Arrowhead Pharmaceuticals
14.73
-13.11
-47.09%
PFE
Pfizer
25.55
-0.41
-1.58%
SRPT
Sarepta Therapeutics
73.61
-54.64
-42.60%
MRNA
Moderna
33.85
-73.56
-68.49%

Silence Therapeutics Earnings Call Summary

Earnings Call Date: Feb 27, 2025 | % Change Since: -24.11% | Next Earnings Date: May 14, 2025
Earnings Call Sentiment Neutral
The earnings call highlighted positive clinical trial results for zerlasiran and divesiran, revenue growth, and an extended cash runway. However, the termination of the Hansoh Pharma collaboration and the delay of the zerlasiran Phase 3 study due to the need for a partner were significant challenges mentioned.
Highlights
Positive Results for Zerlasiran Phase 2 Study
The ALPACAR-360 Phase 2 study of zerlasiran in ASCVD patients with high Lp(a) delivered positive results, showing Lp(a) reductions exceeded 90% and were durable. The study was featured in a late-breaker at AHA and published in JAMA.
Divesiran Phase 1 Success and Phase 2 Progress
The SANRECO’s Phase 1 study of divesiran showed positive results, eliminating the need for phlebotomy in all well-controlled patients. Phase 2 study dosing has started, and the European Commission has granted divesiran Orphan Drug Designation for PV.
Revenue Growth
The company recorded $43.3 million in revenues for 2024, an increase of $11.7 million from 2023, largely due to collaboration arrangements utilizing the siRNA platform.
Extension of Cash Runway
By delaying the Phase 3 study of zerlasiran until a partner is secured, the company has extended its projected cash runway into 2027.
Lowlights
Hansoh Pharma Collaboration Termination
Hansoh Pharma opted not to pursue further development under the collaboration, resulting in the company regaining rights to three undisclosed preclinical liver targets.
Zerlasiran Phase 3 Study Delay
The Phase 3 outcomes study for zerlasiran will only be initiated once a partner is secured, which may delay the advancement of this promising program.
Company Guidance
During the call, Silence Therapeutics provided guidance on several key metrics for their future operations. The company reported $43.3 million in revenues for 2024, an increase from $31.6 million in 2023, largely due to collaboration arrangements. They ended 2024 with $147.3 million in cash, cash equivalents, and short-term investments. Silence announced they would only initiate the Phase 3 outcomes study for zerlasiran, their siRNA for high Lp(a), once a partner is secured, which extends their cash runway into 2027. Additionally, they are prioritizing investment in programs targeting rare conditions, like divesiran for polycythemia vera (PV), which has received orphan drug designation in both the EU and US. The company also plans to commence a Phase 1 study of SLN548 targeting complement factor B in the second half of 2025. Silence transitioned to a U.S. domestic issuer status, moving from IFRS to U.S. GAAP, which resulted in a net loss decrease to $45.3 million in 2024 from $54.2 million in 2023.

Silence Therapeutics Corporate Events

Business Operations and StrategyFinancial Disclosures
Silence Therapeutics Extends Cash Runway to 2027
Positive
Feb 27, 2025

Silence Therapeutics reported its financial results for the year ending December 31, 2024, highlighting strong clinical execution and pipeline advancements. The company plans to prioritize investment in siRNA programs targeting rare conditions, with a focus on the divesiran program for polycythemia vera (PV) and the zerlasiran program for cardiovascular disease. Silence ended the year with $147 million in cash, and its decision to delay the zerlasiran Phase 3 study until a partner is secured extends its cash runway into 2027. The company received positive regulatory feedback for the zerlasiran study design and anticipates full enrollment in the SANRECO Phase 2 study of divesiran by the end of 2025.

Regulatory Filings and Compliance
Silence Therapeutics to Transition to U.S. Issuer Status
Neutral
Jan 2, 2025

Silence Therapeutics will transition to filing reports as a U.S. domestic issuer starting January 1, 2025, which entails using more detailed and prompt SEC forms compared to those for a foreign private issuer. This change reflects the company’s growth and could impact its transparency and engagement with stakeholders, as it also utilizes multiple channels to disseminate material information broadly.

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.