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Intellia Therapeutics Inc (NTLA)
NASDAQ:NTLA
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Intellia Therapeutics (NTLA) AI Stock Analysis

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NTLA

Intellia Therapeutics

(NASDAQ:NTLA)

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Neutral 51 (OpenAI - Gpt-5.6Sol)
Rating:51Neutral
Price Target:
$13.50
▲(25.82% Upside)
Action:Reiterated
Date:08/07/26
NTLA’s score is held back primarily by weak financial performance (large losses and ongoing cash burn) and soft technicals (below key moving averages with negative MACD). These are partly offset by constructive earnings-call fundamentals—strong lonvo-z Phase III results with active regulatory/commercial preparations and a stated cash runway into at least 2028—while valuation remains hard to assess due to negative earnings and no dividend.
Positive Factors
Phase III efficacy and regulatory progress
The strong Phase III efficacy supports lonvo-z’s potential to become a differentiated one-time treatment for hereditary angioedema. The rolling BLA and planned regulatory decision create a clearer path from clinical validation toward commercialization.
Negative Factors
Persistent losses and cash burn
Intellia remains dependent on cash reserves, financing and collaboration funding because its development-stage programs do not yet generate product revenue. Continued high research and commercial spending could require additional capital if launch timing or approvals slip.
Read all positive and negative factors
Positive Factors
Negative Factors
Phase III efficacy and regulatory progress
The strong Phase III efficacy supports lonvo-z’s potential to become a differentiated one-time treatment for hereditary angioedema. The rolling BLA and planned regulatory decision create a clearer path from clinical validation toward commercialization.
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. is a biotechnology firm dedicated to advancing therapeutic treatments through its expertise in genome editing. The company's pipeline includes several in vivo (administered within the body) programs. NTLA-2001 is curren...
How the Company Makes Money
Intellia primarily generates revenue from collaboration and license arrangements with pharmaceutical partners rather than from product sales (as its key programs have been in clinical development and commercialization is limited or not applicable)...

Intellia Therapeutics Earnings Call Summary

Earnings Call Date:Aug 06, 2026
(Q2-2026)
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% Change Since: |
Next Earnings Date:Nov 05, 2026
Earnings Call Sentiment Positive
The call conveyed strong, concrete clinical progress — most notably the unequivocal Phase III success for lonvo‑z (87% attack reduction, 62% attack‑free and therapy‑free, favorable safety) and compelling nex‑z biological data (≈90% TTR knockdown, rapid and durable) — alongside active regulatory and commercial preparations. Financially, the company strengthened its cash position with a ~$195M financing and maintains a runway into at least 2028, although collaboration revenue declined and G&A rose as commercial build‑out continues. The primary concern is a nex‑z liver enzyme safety signal and the identification of an HLA C*05:01 subgroup (~12% of samples) associated with higher Grade 3+ transaminase events; the company has implemented mitigation, added HLA typing to protocols, and is engaging regulators. Overall, the positive clinical milestones and clear mitigation plan for the safety finding outweigh the operational and financial headwinds discussed.
Positive Updates
HAELO Phase III (lonvo-z) — Strong Efficacy
Phase III HAELO achieved statistical significance for the primary and all key secondary endpoints: an 87% reduction in mean monthly attacks versus placebo during the 6-month primary period; 62% of patients were entirely attack-free and therapy-free; and a 23‑point improvement in total angioedema quality‑of‑life score from baseline (vs. 6 points considered clinically meaningful). All patients in the lonvo‑z arm experienced attack rate reductions for weeks 5–28.
Negative Updates
nex‑z Liver Enzyme Safety Signal
Grade 4 liver transaminase elevations have been observed (reported in <1% of MAGNITUDE patients) and Grade 3+ transaminase events occurred; company attributes timing (2–5 weeks post‑dose) to an adaptive immune response and has implemented mitigation and monitoring measures. The safety signal requires continued monitoring and regulatory engagement.
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Q2-2026 Updates
Negative
HAELO Phase III (lonvo-z) — Strong Efficacy
Phase III HAELO achieved statistical significance for the primary and all key secondary endpoints: an 87% reduction in mean monthly attacks versus placebo during the 6-month primary period; 62% of patients were entirely attack-free and therapy-free; and a 23‑point improvement in total angioedema quality‑of‑life score from baseline (vs. 6 points considered clinically meaningful). All patients in the lonvo‑z arm experienced attack rate reductions for weeks 5–28.
Read all positive updates
Company Guidance
Intellia said it expects FDA acceptance of the lonvo‑z BLA by year‑end and is preparing for a potential U.S. launch in H1 2027 (pre‑commercial hires complete); it reported $628.4M cash, cash equivalents and marketable securities as of June 30, 2026 (after ~ $195M net equity financing in April) and believes this funding should carry the company at least into 2028 (conservative, excludes product revenue); Q2 metrics included collaboration revenue $7.7M, R&D $82.6M (stock‑comp $9.4M), G&A $37.8M (stock‑comp $8.6M) and net loss $106.6M; clinical guidance highlighted HAELO topline that showed an 87% reduction in mean monthly attacks vs placebo, 62% of patients attack‑ and therapy‑free, and a 23‑point improvement in angioedema QoL over 6 months (vs a 6‑point meaningful change), while nex‑z dosing resumed in Q2, MAGNITUDE has enrolled >650 patients with a blinded event rate within internal projections and MAGNITUDE‑2 enrollment expected to complete later this year; safety work sequenced >600 samples, found HLA C*05:01 in ~12% of patients and linked it to the highest transaminase elevations (Grade 4 events <1% overall), prompting HLA typing and mitigation measures across ongoing trials, and Phase I nex‑z showed ~90% mean TTR reduction with mean serum TTR <20 µg/mL within 1 month.

Intellia Therapeutics Financial Statement Overview

Summary
Overall fundamentals reflect a development-stage biotech profile: very weak profitability and sizable losses (income statement score 18) plus materially negative operating/free cash flow and recent burn worsening (cash flow score 24). This is partially offset by a comparatively strong, low-leverage balance sheet (balance sheet score 66) that supports near-term flexibility.
Income Statement
18
Very Negative
Balance Sheet
66
Positive
Cash Flow
24
Negative
BreakdownTTMDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue59.51M67.67M57.88M36.27M52.12M33.05M
Gross Profit-27.66M51.75M47.59M27.30M44.55M26.16M
EBITDA-390.36M-396.77M-508.74M-472.22M-466.61M-261.00M
Net Income-399.98M-412.69M-519.02M-481.19M-474.19M-267.89M
Balance Sheet
Total Assets857.16M842.13M1.19B1.30B1.52B1.29B
Cash, Cash Equivalents and Short-Term Investments437.76M449.88M601.51M912.22M1.19B748.69M
Total Debt73.41M93.33M210.20M115.35M130.70M74.02M
Total Liabilities129.46M170.73M319.06M250.81M284.53M254.22M
Stockholders Equity727.71M671.39M871.96M1.05B1.24B1.04B
Cash Flow
Free Cash Flow-466.11M-354.66M-354.66M-408.07M-391.68M-237.79M
Operating Cash Flow-463.99M-348.88M-348.88M-394.09M-333.29M-225.03M
Investing Cash Flow17.84M125.57M125.57M-31.35M160.31M-550.78M
Financing Cash Flow380.09M185.75M185.75M130.32M582.96M736.69M

Intellia Therapeutics Technical Analysis

Technical Analysis Sentiment
Positive
Last Price10.73
Price Trends
50DMA
13.32
Positive
100DMA
13.48
Positive
200DMA
12.42
Positive
Market Momentum
MACD
0.09
Negative
RSI
59.34
Neutral
STOCH
74.50
Neutral
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 10.73 is below the 20-day moving average (MA) of 11.85, below the 50-day MA of 13.32, and below the 200-day MA of 12.42, indicating a bullish trend. The MACD of 0.09 indicates Negative momentum. The RSI at 59.34 is Neutral, neither overbought nor oversold. The STOCH value of 74.50 is Neutral, 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
56
Neutral
$3.44B-23.15-17.49%101.28%2.49%
56
Neutral
$1.14B-11.34-10.79%5366.97%8.50%
56
Neutral
$1.56B-7.61-41.49%-63.70%
54
Neutral
$1.10B-4.03-207.18%-7.27%-48.89%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
51
Neutral
$1.76B-3.74-57.79%12.58%28.42%
45
Neutral
$432.21M-5.78-38.71%10.44%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
NTLA
Intellia Therapeutics
13.51
2.15
18.93%
KURA
Kura Oncology
13.59
6.01
79.29%
CMPX
Compass Therapeutics
2.53
-0.62
-19.68%
ABCL
AbCellera Biologics
12.50
8.13
186.04%
JANX
Janux Therapeutics Inc
18.68
-4.96
-20.98%
BCAX
Bicara Therapeutics Inc.
24.58
12.54
104.15%

Intellia Therapeutics Corporate Events

Business Operations and StrategyProduct-Related AnnouncementsRegulatory Filings and Compliance
Intellia Highlights Strong Phase 3 Lonvo-z HAE Results
Positive
Jun 15, 2026
On June 13, 2026, Intellia Therapeutics reported additional positive Phase 3 results from its global HAELO trial of lonvo-z for hereditary angioedema, presented at the EAACI 2026 Congress in Istanbul and published in the New England Journal of Med...
Executive/Board ChangesShareholder Meetings
Intellia Shareholders Back Board, Executive Pay and Auditor
Positive
Jun 10, 2026
On June 9, 2026, Intellia Therapeutics, Inc. held its Annual Meeting at which stockholders elected Muna Bhanji, R.Ph., Brian Goff and Jesse Goodman, M.D., M.P.H., as Class I directors for three-year terms ending at the 2029 annual meeting. Stockho...
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: Aug 07, 2026