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Intellia Therapeutics (NTLA)
NASDAQ:NTLA

Intellia Therapeutics (NTLA) AI Stock Analysis

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NTLA

Intellia Therapeutics

(NASDAQ:NTLA)

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Neutral 53 (OpenAI - 5.2)
Rating:53Neutral
Price Target:
$14.00
▼(-5.28% Downside)
Action:ReiteratedDate:04/11/26
The score is held back primarily by weak financial performance—persistent losses, volatile revenue, and ongoing cash burn—despite a comparatively solid solvency profile. Technicals are moderately supportive with price above key moving averages and positive MACD. Clinical/program progress and reiterated timelines from the earnings call help, but safety/regulatory uncertainty and funding/dilution considerations temper the outlook.
Positive Factors
Pivotal lonvo‑z Phase 3 readout and planned BLA
Completing Phase 3 enrollment and targeting a mid‑2026 pivotal readout with a planned H2‑2026 BLA is a durable operational inflection. A successful outcome would transition Intellia toward commercial revenues, validate its in vivo CRISPR platform, and materially expand long‑term strategic and partnership optionality.
Negative Factors
Persistent cash burn and negative cash flow
Sustained negative operating and free cash flow indicates the company relies on financing and collaborations to fund R&D. Persistent cash burn depletes equity, narrows strategic flexibility, and raises the probability of future dilution or constrained investment in other pipeline programs absent new non‑dilutive funding.
Read all positive and negative factors
Positive Factors
Negative Factors
Pivotal lonvo‑z Phase 3 readout and planned BLA
Completing Phase 3 enrollment and targeting a mid‑2026 pivotal readout with a planned H2‑2026 BLA is a durable operational inflection. A successful outcome would transition Intellia toward commercial revenues, validate its in vivo CRISPR platform, and materially expand long‑term strategic and partnership optionality.
Read all positive factors

Intellia Therapeutics (NTLA) vs. SPDR S&P 500 ETF (SPY)

Intellia Therapeutics Business Overview & Revenue Model

Company Description
Intellia Therapeutics, Inc., a genome editing company, focuses on the development of therapeutics. The company's in vivo programs include NTLA-2001, which is in Phase 1 clinical trial for the treatment of transthyretin amyloidosis; and NTLA-2002 f...
How the Company Makes Money
Intellia Therapeutics has historically generated revenue primarily from collaboration and license arrangements rather than from product sales, because it is a clinical-stage company without widely commercialized therapies. Key revenue streams incl...

Intellia Therapeutics Earnings Call Summary

Earnings Call Date:Feb 26, 2026
(Q4-2025)
|
% Change Since: |
Next Earnings Date:Apr 30, 2026
Earnings Call Sentiment Neutral
The call presents a mix of important clinical and commercial progress — most notably the completed Phase 3 enrollment and upcoming pivotal readout for lonvo-z, strong patient and physician interest, durable early efficacy signals, and improved near-term financial metrics — alongside meaningful risks: a still-pending FDA hold on the large cardiomyopathy ATTR program driven by serious liver enzyme events (including one patient death), material year-over-year cash depletion, and incomplete understanding of the safety signal’s mechanism and breadth. Management has secured a partial regulatory win (MAGNITUDE-2 hold lifted with specific mitigations) and emphasizes preparedness for a potential lonvo-z launch, but the unresolved MAGNITUDE hold and safety uncertainty inject non-trivial downside risk.
Positive Updates
Lonvo-z Phase 3 Enrollment and Imminent Readout
Completed enrollment of the HAELO Phase 3 trial with 80 patients in ~9 months; top-line data expected by mid-2026 and a planned BLA submission in H2 2026 — positioning Intellia for the world’s first pivotal readout for an in vivo CRISPR gene-editing therapy.
Negative Updates
Clinical Hold on MAGNITUDE (Cardiomyopathy) Remains
MAGNITUDE (ATTR-CM) remains on clinical hold after elevated liver transaminases and total bilirubin observed in a patient; while the company is actively engaged with the FDA and has proposed mitigations, the hold has not yet been lifted, creating uncertainty for a large cardimyopathy cohort that had already enrolled >650 patients (vs ~550 expected).
Read all updates
Q4-2025 Updates
Negative
Lonvo-z Phase 3 Enrollment and Imminent Readout
Completed enrollment of the HAELO Phase 3 trial with 80 patients in ~9 months; top-line data expected by mid-2026 and a planned BLA submission in H2 2026 — positioning Intellia for the world’s first pivotal readout for an in vivo CRISPR gene-editing therapy.
Read all positive updates
Company Guidance
Management reiterated guidance for a big 2026 year: top‑line phase 3 lonvo‑z data by mid‑2026, a planned BLA submission in H2‑2026 and a potential launch in 2027; HAELO is fully enrolled (80 patients) and pooled data show 76% of patients ≥1 year post‑50 mg were attack‑free ≥12 months (versus ~20% attack‑free on current therapies), while market research (104 patients, 151 HCPs) showed 99% of patients would be at least somewhat likely to take lonvo‑z, 92% of HCPs could identify a patient, and physicians collectively manage ~4,000 patients (~60% of the U.S. treated population) and would prescribe to ~2,200 (54%). For ATTR, MAGNITUDE had >650 patients enrolled before the October hold, MAGNITUDE‑2 has 47 enrolled with a revised target of ~60 and is expected to complete enrollment in H2‑2026 after the FDA lifted the MAGNITUDE‑2 hold in late January; mitigation measures (extra LFT monitoring and short‑term steroid regimens) were agreed given a Grade‑4 LFT incidence of <1%. Financially, cash, cash equivalents and marketable securities were $605.1M at 12/31/25 (down from $861.7M a year earlier) with runway into H2‑2027, Q4 collaboration revenue was $23M, R&D was $88.7M (stock‑based comp $10.5M), G&A $33.1M (stock‑based comp $6.2M) and Q4 net loss was $95.8M (vs $128.9M prior year).

Intellia Therapeutics Financial Statement Overview

Summary
Overall financial quality is pressured by sustained large net losses and consistently negative operating/free cash flow (ongoing cash burn). The balance sheet is a relative strength with modest leverage and reported cash runway into H2-2027, but equity has trended down amid continued deficits and revenue has been volatile (including zero in 2025 annual).
Income Statement
18
Very Negative
Balance Sheet
62
Positive
Cash Flow
27
Negative
BreakdownDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue67.67M57.88M36.27M52.12M33.05M
Gross Profit51.75M47.59M27.30M44.55M26.16M
EBITDA-396.77M-523.98M-506.31M-450.59M-260.96M
Net Income-412.69M-519.02M-481.19M-474.19M-267.89M
Balance Sheet
Total Assets842.13M1.19B1.30B1.52B1.29B
Cash, Cash Equivalents and Short-Term Investments449.88M601.51M912.22M1.19B748.69M
Total Debt93.33M210.20M115.35M130.70M74.02M
Total Liabilities170.73M319.06M250.81M284.53M254.22M
Stockholders Equity671.39M871.96M1.05B1.24B1.04B
Cash Flow
Free Cash Flow-354.66M-354.66M-408.07M-391.68M-237.79M
Operating Cash Flow-348.88M-348.88M-394.09M-333.29M-225.03M
Investing Cash Flow125.57M125.57M-31.35M160.31M-550.78M
Financing Cash Flow185.75M185.75M130.32M582.96M736.69M

Intellia Therapeutics Technical Analysis

Technical Analysis Sentiment
Positive
Last Price14.78
Price Trends
50DMA
13.09
Positive
100DMA
11.70
Positive
200DMA
12.94
Positive
Market Momentum
MACD
0.29
Negative
RSI
62.70
Neutral
STOCH
80.86
Negative
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For NTLA, the sentiment is Positive. The current price of 14.78 is above the 20-day moving average (MA) of 13.27, above the 50-day MA of 13.09, and above the 200-day MA of 12.94, indicating a bullish trend. The MACD of 0.29 indicates Negative momentum. The RSI at 62.70 is Neutral, neither overbought nor oversold. The STOCH value of 80.86 is Negative, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Positive sentiment for NTLA.

Intellia Therapeutics Risk Analysis

Intellia Therapeutics disclosed 1 risk factors in its most recent earnings report. Intellia Therapeutics reported the most risks in the "Production" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 1 New Risks
1.
Governance Q4, 2025

Intellia Therapeutics Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
62
Neutral
$1.45B-6.67-32.49%-103.95%
53
Neutral
$1.68B-2.54-56.63%33.52%21.66%
52
Neutral
$770.24M-3.27-102.59%-5.18%
52
Neutral
$936.46M-12.74-43.61%-100.00%-28.79%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
50
Neutral
$908.22M-11.55%-23.37%-42.45%
49
Neutral
$1.11B-6.98-14.16%7.16%3.95%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
NTLA
Intellia Therapeutics
14.78
7.42
100.82%
KURA
Kura Oncology
9.14
3.11
51.58%
CMPX
Compass Therapeutics
5.44
3.74
220.00%
ABCL
AbCellera Biologics
3.76
1.33
54.73%
JANX
Janux Therapeutics Inc
15.24
-13.82
-47.56%
BCAX
Bicara Therapeutics Inc.
22.98
11.53
100.70%

Intellia Therapeutics Corporate Events

Business Operations and StrategyRegulatory Filings and Compliance
Intellia Therapeutics Adopts Fourth Amended and Restated Bylaws
Positive
Apr 10, 2026
On April 7, 2026, Intellia Therapeutics, Inc.&#8217;s board of directors adopted amendments to its by-laws to create a Fourth Amended and Restated By-law framework, following a recommendation from its nominating and corporate governance committee....
Business Operations and StrategyPrivate Placements and FinancingRegulatory Filings and Compliance
Intellia Resumes Key Trial and Expands ATM Program
Positive
Mar 2, 2026
On March 2, 2026, Intellia Therapeutics, Inc. amended its at-the-market equity offering agreement with Jefferies LLC, raising the total program size from $750 million to about $1.04 billion and filing a new prospectus supplement to cover up to $40...
Business Operations and StrategyProduct-Related AnnouncementsRegulatory Filings and Compliance
FDA Lifts Hold on Intellia’s MAGNITUDE-2 Trial
Neutral
Jan 27, 2026
On January 27, 2026, Intellia Therapeutics announced that the U.S. Food and Drug Administration lifted the clinical hold on its investigational new drug application for the MAGNITUDE-2 Phase 3 trial of nexiguran ziclumeran in patients with heredit...
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: Apr 11, 2026