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Paused Trials Will Drive Rebound After Resolution Of Safety Concerns

Published
25 Mar 25
Updated
12 Nov 25
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AnalystConsensusTarget's Fair Value
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1Y
-42.6%
7D
-5.6%

Author's Valuation

US$24.8567.0% undervalued intrinsic discount

AnalystConsensusTarget Fair Value

Last Update 12 Nov 25

Fair value Decreased 23%

NTLA: Phase 3 Enrollment Milestones And Data Readouts Will Drive Next Upside

Analysts have reduced their fair value estimate for Intellia Therapeutics from approximately $32.30 to $24.85. They cite heightened safety concerns in key clinical programs and lower projected growth rates following recent adverse events and subsequent trial pauses.

Analyst Commentary

Recent analyst activity reflects a climate of both caution and cautious optimism regarding Intellia Therapeutics, following safety events and trial pauses across key programs. The valuation outlook has shifted due to clinical uncertainties; however, some analysts continue to highlight select opportunities within the company’s pipeline.

Bullish Takeaways

  • Bullish analysts highlight Intellia’s ongoing progress in the hereditary angioedema program, noting strong survey interest and potential for meaningful market share in a one-time prophylactic therapy.
  • Several maintain positive ratings and price targets, arguing that current valuation may over-discount setbacks in single programs while overlooking upside in other clinical candidates.
  • Enrollment completion in pivotal Phase 3 trials and near-term data readouts are seen as significant milestones for valuation recovery and growth potential.
  • Despite broader concerns, some see the temporary trial pauses as addressable and believe the company’s technology retains differentiated long-term promise in gene editing.

Bearish Takeaways

  • Bearish analysts highlight increased uncertainty around the company’s growth trajectory and clinical execution after multiple severe liver toxicity events and a subsequent patient death, which led to regulatory and voluntary trial holds.
  • Price targets have been sharply reduced across the board amid doubts about the risk/benefit profile of its lead cardiomyopathy program, especially where safer therapeutic alternatives exist.
  • Caution is mounting over delays and the potential for further regulatory intervention, which could delay approvals and dampen confidence in the gene-editing platform’s safety.
  • Many now question the visibility to valuation upside in the near term, given program removals from financial models and a narrowed path to recovery based on current information.

What's in the News

  • Intellia announced positive follow-up data from its ongoing Phase 1 trial of nexiguran ziclumeran (nex-z) for transthyretin (ATTR) amyloidosis with cardiomyopathy. The data show disease stabilization or improvement at 24 months and continued strong TTR reduction. (Company announcement)
  • The U.S. Food and Drug Administration placed a clinical hold on the MAGNITUDE and MAGNITUDE 2 Phase 3 trials of nex-z following a serious liver adverse event. Intellia is working to resolve the hold and resume studies. (Company announcement)
  • Intellia presented positive pooled clinical data for its gene-editing therapy lonvoguran ziclumeran (lonvo-z) in hereditary angioedema. At 24 months after treatment, 97% of patients were attack-free. (Company announcement)
  • Enrollment has been completed for the global Phase 3 HAELO study of lonvo-z for hereditary angioedema. A U.S. biologics license application filing is planned for the second half of 2026, with a targeted launch in 2027. (Company announcement)
  • Longer-term data from the ongoing Phase 1 trial of nex-z for hereditary ATTR amyloidosis with polyneuropathy indicated deep and durable reductions in serum TTR and signs of improvement or stability in clinical measures for up to three years. (Company announcement)

Valuation Changes

  • Fair Value Estimate: Lowered from approximately $32.30 to $24.85 per share. This reflects a significant downward revision in the company's assessed worth.
  • Discount Rate: Increased slightly from 6.95% to 7.13%. This indicates perceived higher risk associated with future cash flows.
  • Revenue Growth: Reduced from 130.0% to 114.5%. This signals more conservative expectations for top-line expansion.
  • Net Profit Margin: Decreased from 16.33% to 14.36%. This reflects predictions of thinner future profitability.
  • Future Price-to-Earnings (P/E) Ratio: Increased from 47.0x to 52.8x. This suggests that despite lower growth and margins, shares remain at a relatively high forward valuation multiple.

Key Takeaways

  • Accelerated clinical progress and expanding market opportunities position Intellia for earlier commercialization and significant long-term revenue growth.
  • Improved financial discipline and strong clinical validation support sustainable margins, enhanced payer acceptance, and recurring revenue from commercialization and partnerships.
  • Competitive pressures, high development costs, pipeline concentration, and reimbursement barriers threaten Intellia's growth, profitability, and ability to sustain its technological edge over time.

Catalysts

About Intellia Therapeutics
    A clinical-stage gene editing company, focuses on the development of curative genome editing treatments.
What are the underlying business or industry changes driving this perspective?
  • Growing patient and physician enthusiasm for Intellia's lead in vivo CRISPR therapies is driving faster-than-expected enrollment across multiple late-stage clinical trials (including an expanded 1,200-patient ATTR cardiomyopathy study and strong uptake in HAE), positioning the company to achieve meaningful clinical readouts and regulatory milestones ahead of prior guidance-this advances timelines to potential commercialization, driving long-term revenue growth prospects.
  • The sustained expansion of the addressable market for Intellia's programs is reinforced by demographic trends-especially aging populations and the continued rise in genetic and chronic conditions like ATTR amyloidosis and HAE-supporting higher future patient volumes and underpinning potential multi-launch revenue inflection points.
  • Improving financial discipline, as evidenced by successful restructuring, declining GAAP operating expenses (~10% reduction YoY), and a robust cash runway into the first half of 2027, enables Intellia to absorb increased R&D investment, advance pipeline expansion, and build out commercial infrastructure without dilutive fundraising, supporting protection of net margins and improving future earnings visibility.
  • Strengthening real-world validation of the company's platform-with mature clinical data showing durable, attack-free results in HAE and deep TTR reductions plus positive functional outcomes in ATTR-should bolster pricing power, enhance payer acceptance, and create leverage for value-based reimbursement, directly benefiting gross margins and long-term profitability.
  • Rapid technological and regulatory advancements in gene-editing-including increased healthcare investments, accelerating review pathways, and support for first-in-class CRISPR therapies-create a favorable environment for Intellia's platform to secure approvals, forge additional partnership/licensing opportunities, and achieve sustainable, recurring non-dilutive revenues through both commercialization and collaborations, increasing top-line growth and earnings potential.

Intellia Therapeutics Earnings and Revenue Growth

Intellia Therapeutics Future Earnings and Revenue Growth

Assumptions

How have these above catalysts been quantified?
  • Analysts are assuming Intellia Therapeutics's revenue will grow by 130.7% annually over the next 3 years.
  • Analysts are not forecasting that Intellia Therapeutics will become profitable in next 3 years. To represent the Analyst Price Target as a Future PE Valuation we will estimate Intellia Therapeutics's profit margin will increase from -908.5% to the average US Biotechs industry of 16.1% in 3 years.
  • If Intellia Therapeutics's profit margin were to converge on the industry average, you could expect earnings to reach $104.2 million (and earnings per share of $0.83) by about September 2028, up from $-480.2 million today. However, there is a considerable amount of disagreement amongst the analysts with the most bullish expecting $2.7 billion in earnings, and the most bearish expecting $-597.2 million.
  • In order for the above numbers to justify the analysts price target, the company would need to trade at a PE ratio of 49.8x on those 2028 earnings, up from -2.6x today. This future PE is greater than the current PE for the US Biotechs industry at 15.5x.
  • Analysts expect the number of shares outstanding to grow by 5.4% per year for the next 3 years.
  • To value all of this in today's terms, we will use a discount rate of 6.78%, as per the Simply Wall St company report.

Intellia Therapeutics Future Earnings Per Share Growth

Intellia Therapeutics Future Earnings Per Share Growth

Risks

What could happen that would invalidate this narrative?
  • Mounting competition from alternative gene therapy and RNAi approaches-including established and newly launched therapies in ATTR amyloidosis and HAE-could limit nex-z and lonvo-z's market share and weaken Intellia's pricing power, impacting long-term revenue growth and gross margins.
  • Reliance on major late-stage clinical trial results for limited lead programs (nex-z, lonvo-z) creates revenue concentration risk; any regulatory, clinical, or safety setbacks could significantly delay or diminish future earnings and long-term profitability.
  • High R&D expenses and ongoing cash burn, combined with no near-term commercial product revenues, raise the risk of shareholder dilution or funding constraints, potentially pressuring net margins and earnings despite current cash runway guidance.
  • Payer scrutiny and reimbursement challenges for costly, potentially one-time gene-editing therapies-especially in crowded indications-could limit uptake, slow commercial ramp, and jeopardize expected revenue streams.
  • Advances in other gene editing or treatment modalities (such as prime editing, base editing, or more effective RNAi) could erode Intellia's technological lead, making its CRISPR platform less differentiated over the long term, which would negatively affect revenue growth and long-term valuation.

Valuation

How have all the factors above been brought together to estimate a fair value?
  • The analysts have a consensus price target of $34.083 for Intellia Therapeutics based on their expectations of its future earnings growth, profit margins and other risk factors. However, there is a degree of disagreement amongst analysts, with the most bullish reporting a price target of $106.0, and the most bearish reporting a price target of just $7.0.
  • In order for you to agree with the analyst's consensus, you'd need to believe that by 2028, revenues will be $648.6 million, earnings will come to $104.2 million, and it would be trading on a PE ratio of 49.8x, assuming you use a discount rate of 6.8%.
  • Given the current share price of $11.71, the analyst price target of $34.08 is 65.6% higher.
  • We always encourage you to reach your own conclusions though. So sense check these analyst numbers against your own assumptions and expectations based on your understanding of the business and what you believe is probable.

How well do narratives help inform your perspective?

Disclaimer

AnalystConsensusTarget is a tool utilizing a Large Language Model (LLM) that ingests data on consensus price targets, forecasted revenue and earnings figures, as well as the transcripts of earnings calls to produce qualitative analysis. The narratives produced by AnalystConsensusTarget are general in nature and are based solely on analyst data and publicly-available material published by the respective companies. These scenarios are not indicative of the company's future performance and are exploratory in nature. Simply Wall St has no position in the company(s) mentioned. Simply Wall St may provide the securities issuer or related entities with website advertising services for a fee, on an arm's length basis. These relationships have no impact on the way we conduct our business, the content we host, or how our content is served to users. The price targets and estimates used are consensus data, and do not constitute a recommendation to buy or sell any stock, and they do not take account of your objectives, or your financial situation. Note that AnalystConsensusTarget's analysis may not factor in the latest price-sensitive company announcements or qualitative material.

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