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Forecast
The analysts' average price target is €16.48 (+83.31%). The median is €16.78 (+86.65%).
| Buy |
29 |
| Hold |
7 |
| Sell |
3 |
Discussions in the community
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ARK Invest expands position in Intellia Therapeutics and reduces Brera holding
ARK Invest increased its position in Intellia Therapeutics by 89,284 shares worth about 1.09 million USD via the ETFs ARKK and ARKG. At the same time, ARK sold 4,156 shares of Brera Holdings for approximately 15,377 USD through ARKK, ARKW and ARKF. ARK also bought shares of the 3iQ Solana Staking ETF (4,021 shares, about 33,615 USD), reflecting a strategic focus on biotechnology and selective investments in crypto assets. » More on de.investing.com
Intellia Therapeutics receives FDA priority review for lonvo-z, stock rises
The FDA has formally accepted the Biologics License Application (BLA) for lonvoguran ziclumeran (lonvo-z) and granted a priority review; the PDUFA date is March 10, 2027. A decision by an advisory committee is not currently planned, reducing regulatory uncertainty. The filing is based on strong Phase 3 data from the HAELO study showing a median reduction in monthly HAE attacks of 87% and 62% of patients attack-free over six months. Analysts reaffirmed a "Market Outperform" rating with a $30.00 price target, creating a near-term catalyst for the stock. » More on de.investing.com
ARK increases stake in Intellia Therapeutics and reduces Brera positions
Cathie Wood’s ARK bought 39,548 shares of Intellia Therapeutics on September 3 via the ARKG ETF for about $504,632, continuing a series of increases started in the days before. At the same time, ARK sold a total of 10,853 shares of Brera Holdings across several ETFs for roughly $41,241, further trimming the position in recent days. The transactions reflect a strategic reallocation in favor of Intellia and a reduction of exposure to Brera. » More on de.investing.com
Intellia shows strong phase‑3 data for CRISPR gene therapy lonvo‑z against hereditary angioedema
Intellia presented phase‑3 data from the HAELO study showing lonvo‑z reduced the monthly rate of attacks requiring treatment between weeks 5 and 28 by 89% versus placebo (0.19 vs. 1.79). Moderate to severe attacks fell by 91% and quality of life improved substantially more than with placebo. Adverse events were mostly mild to moderate, and no serious events were reported in the treatment arm. Intellia has filed a rolling BLA with the FDA and expects approval and a U.S. launch in the first half of 2027, while the stock has recently fallen despite the data. » More on de.investing.com
Intellia share price falls after $180 million capital raise at steep discount
The Intellia share dropped more than 8% in premarket trading to $12.09 after the company placed roughly 16.7 million shares at $10.75 each. The offering was increased from an initial $150 million to $180 million and was conducted at an 18.6% discount to the closing price. Proceeds are intended to finance clinical development, the commercialization of lead programs, R&D of additional candidates, and potential acquisitions. » More on de.investing.com
Historical dividends Dividends
All dividend metrics All metricsFinancials
| (EUR) | September 2026 | YoY |
|---|---|---|
| Revenue | 6.32m | 46.15% |
| Gross profit | 6.32m | 111.39% |
| Net profit | -112.55m | 30.36% |
| EBITDA | -112.01m | 36.37% |
Fundamentals
| Metric | Value |
|---|---|
Market capitalization | €1.24bn |
Number of shares | 140.36m |
52-week high/low | €16.76 - €7.21 |
| Dividends | No |
Beta | 1.82 |
P/E ratio | -2.90 |
PEG ratio | -0.12 |
P/B ratio | 2.22 |
P/S ratio | 25.74 |
Company profile
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 for the treatment of hereditary angioedema, as well as other liver-focused programs comprising hemophilia A and hemophilia B, hyperoxaluria Type 1, and alpha-1 antitrypsin deficiency. Its ex vivo pipeline includes NTLA-5001 for the treatment of acute myeloid leukemia; and proprietary programs focused on developing engineered cell therapies to treat various oncological and autoimmune disorders. In addition, it offers tools comprising of Clustered, Regularly Interspaced Short Palindromic Repeats/CRISPR associated 9 (CRISPR/Cas9) system. Intellia Therapeutics, Inc. has license and collaboration agreements with Novartis Institutes for BioMedical Research, Inc. to engineer hematopoietic stem cells for the treatment of sickle cell disease; Regeneron Pharmaceuticals, Inc. to co-develop potential products for the treatment of hemophilia A and hemophilia B; Ospedale San Raffaele; and a strategic collaboration with SparingVision SAS to develop novel genomic medicines utilizing CRISPR/Cas9 technology for the treatment of ocular diseases. The company was formerly known as AZRN, Inc. Intellia Therapeutics, Inc. was incorporated in 2014 and is headquartered in Cambridge, Massachusetts.
| Name | Intellia Therapeutics |
| CEO | John Leonard |
| Headquarters | Cambridge,
ma USA |
| Website | |
| Sector | Health Care |
| Industry | Life Sciences Tools & Services |
| IPO | 06/05/2016 |
| Employees | 377 |
Ticker symbols
| Exchange | Symbol |
|---|---|
NASDAQ | NTLA |
London Stock Exchange | 0JBU.L |
Frankfurt | 38I.F |
Düsseldorf | 38I.DU |
London | 0JBU.L |
SIX | 38I.SW |
München | 38I.MU |