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NTLA

Intellia Therapeutics

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Prognose

Analytikernes gennemsnitlige kursmål er 18,69 € (+81,63 %). Medianen er 15,34 € (+49,08 %).

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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. » Mere på 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. » Mere på 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. » Mere på 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. » Mere på 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. » Mere på de.investing.com

I 2022 har Intellia Therapeutics allerede udloddet 0,26 € i udbytte. Den seneste udlodning fandt sted i marts 2022.

Virksomhedstal

I det seneste kvartal havde Intellia Therapeutics en omsætning på 6,32 mio. € og et nettoresultat på -112,55 mio. €
(EUR) september 2026
YoY
Omsætning 6,32 mio. 46,15 %
Bruttofortjeneste 6,32 mio. 111,39 %
Nettoresultat -112,55 mio. 30,36 %
EBITDA -112,01 mio. 36,37 %

Fundamentale data

Nøgletal Værdi
Markedsværdi
1,45 mia. €
Antal aktier
140,36 mio.
Højeste/laveste i 52 uger
25,49 € - 6,16 €
Udbytte Nej
Beta
1,82
P/E (PE Ratio)
-3,42
PEG (PEG Ratio)
-0,14
K/I (PB Ratio)
2,62
P/S (PS Ratio)
30,39

Virksomhedsprofil

Intellia Therapeutics, Inc., et genredigeringsselskab, fokuserer på udviklingen af terapeutiske produkter. Selskabets in vivo-programmer omfatter NTLA-2001, som er i fase 1 klinisk forsøg til behandling af transthyretin-amyloidose; og NTLA-2002 til behandling af hereditært angioødem, samt andre leverfokuserede programmer, der omfatter hæmofili A og hæmofili B, hyperoxaluri type 1 og alfa-1-antitrypsinmangel. Dets ex vivo-pipeline omfatter NTLA-5001 til behandling af akut myeloid leukæmi; og proprietære programmer, der fokuserer på udvikling af konstruerede cellulære terapier til behandling af forskellige onkologiske og autoimmune sygdomme. Derudover tilbyder selskabet værktøjer, der omfatter Clustered, Regularly Interspaced Short Palindromic Repeats/CRISPR associated 9 (CRISPR/Cas9)-systemet. Intellia Therapeutics, Inc. har licens- og samarbejdsaftaler med Novartis Institutes for BioMedical Research, Inc. om at konstruere hæmatopoietiske stamceller til behandling af seglcelleanæmi; Regeneron Pharmaceuticals, Inc. om at udvikle potentielle produkter i fællesskab til behandling af hæmofili A og hæmofili B; Ospedale San Raffaele; og et strategisk samarbejde med SparingVision SAS om at udvikle nye genomiske lægemidler ved hjælp af CRISPR/Cas9-teknologi til behandling af øjensygdomme. Selskabet var tidligere kendt som AZRN, Inc. Intellia Therapeutics, Inc. blev stiftet i 2014 og har hovedsæde i Cambridge, Massachusetts.

Navn
Intellia Therapeutics
CEO
John Leonard
Hjemsted Cambridge, ma
USA
Websted
Sektor
Sundhed
Branche
Biovidenskab: værktøjer og tjenester
Børsnotering
06.05.2016
Medarbejdere 377

Tickersymboler

Børs Symbol
NASDAQ
NTLA
London Stock Exchange
0JBU.L
Frankfurt
38I.F
Düsseldorf
38I.DU
London
0JBU.L
SIX
38I.SW
München
38I.MU
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