Last Update 26 Nov 25
Fair value Decreased 9.72%NTLA: Positive Phase 3 Data And Upcoming Regulatory Filing Will Drive Future Upside
Analysts have lowered their average price target on Intellia Therapeutics from approximately $24.85 to $22.43 per share. They cited heightened safety concerns related to recent clinical trial liver toxicity events and uncertainty about the future of key pipeline programs.
Analyst Commentary
Recent analyst actions have reflected significant changes in sentiment around Intellia Therapeutics, with a notable shift driven by safety events and clinical uncertainties. These shifts have prompted both downgrades and target reductions. However, some pockets of optimism remain regarding the company's long-term prospects and pipeline opportunities.
Bullish Takeaways
- Bullish analysts highlight Intellia's potential for significant market share with its once-and-done gene editing therapies, particularly for hereditary angioedema. This suggests a multi-billion dollar commercial opportunity ahead.
- Phase 3 data and regulatory submission timelines for lead programs remain key milestones. Expectations of enrollment completion and data readouts support a positive outlook for future growth.
- Some believe the market may be overreacting to a single-program safety issue, suggesting that current share price levels could offer an attractive entry point if safety can be adequately addressed.
- Despite the setback, certain analysts maintain their buy ratings, anticipating that pause-related delays may be modest and believing that the underlying science and therapeutic approach remain compelling.
Bearish Takeaways
- Bearish analysts have expressed growing concern over trial-related severe liver toxicity events, viewing these as materially increasing execution and regulatory risk across key clinical programs.
- There is increased skepticism about the likelihood of approval and commercial success for affected indications. Several price targets have been materially lowered to reflect uncertainty and a less favorable risk/benefit profile.
- Following negative trial updates, many have downgraded their ratings, citing the cumulative impact of safety events and the pause in patient dosing. This could erode investor confidence and limit near-term upside.
- Some point out that safer treatment alternatives for the affected indications may gain preference. This makes it difficult to see a path forward for certain pipeline programs and increases pressure on valuation and growth expectations.
What's in the News
- Positive follow-up data announced from the ongoing Phase 1 clinical trial of investigational nexiguran ziclumeran (nex-z) in patients with transthyretin amyloidosis with cardiomyopathy. Nex-z showed evidence of disease stabilization or improvement at 24 months and was generally well tolerated. (Company announcement)
- The U.S. FDA placed a clinical hold on the MAGNITUDE and MAGNITUDE 2 Phase 3 trials for nex-z following a reported case of severe liver toxicity in a patient, halting patient dosing and screening. (Company announcement)
- Intellia completed enrollment in the global Phase 3 HAELO study of lonvoguran ziclumeran (lonvo-z) for hereditary angioedema and plans to submit a biologics license application in the second half of 2026, targeting a U.S. launch in 2027. (Company announcement)
- Pooled analysis from Intellia's ongoing Phase 1/2 trial in hereditary angioedema shows 97% of patients treated with a one-time 50 mg dose of lonvo-z remained attack-free at 24 months. (Company announcement)
- Longer-term follow-up results from the Phase 1 study of nex-z for hereditary ATTR amyloidosis with polyneuropathy showed deep and durable serum TTR reduction with most patients experiencing stability or improvement in disease-related measures. (Company announcement)
Valuation Changes
- Consensus Analyst Price Target has fallen from $24.85 to $22.43 per share. This reflects a notable reduction in fair value estimates.
- Discount Rate has risen slightly from 7.13% to 7.20%. Analysts now see greater risk in future cash flows.
- Revenue Growth projections are largely unchanged, moving marginally from 114.50% to 114.39%. This suggests continued high growth expectations.
- Net Profit Margin forecast has increased from 14.36% to 16.03%. This signals modest optimism around future profitability.
- Future P/E multiple has decreased significantly from 52.83x to 42.89x. This indicates lower anticipated earnings multiples due to recent developments.
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.
- 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 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
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.

