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Intellia Therapeutics 2024

337 Posts
Pagina: «« 1 ... 11 12 13 14 15 ... 17 »» | Laatste | Omlaag ↓
  1. Derwing 13 september 2024 10:36
    Lijkt me oprecht interessant en zie ook echt wel potentie voor CRISPR als therapie. Maar ik vind het bedrijf best wel hoog gewaardeerd momenteel. Tot nu toe slechte ervaringen met bedrijven die de mooiste dingen beloven en waar de onderzoeksresultaten er ook echt goed uitzien, maar waarvan het allemaal nog ver weg ligt. Vaak worden kansen op goedkeuring en uiteindelijke omzet/winst niet helemaal realistisch ingeschat van te voren. Ik heb mezelf al te vaak gestoten aan bedrijven waarvan ik dacht dat er echt niks mis kon gaan en 'te mooi is maar wel waar'. Ik vrees dat dit nog heel lang zijwaarts gaat bewegen, of met een beetje pech door jaarlijkse R&D verliezen/dilution en duik omlaag maakt. Ik denk dat je over X jaar nog steeds voor minstens dezelfde prijs kan instappen. Enige risico is dat er inderdaad uiteindelijk een BO komt, maar die kans wordt ook vaak veel te hoog ingeschat.
  2. Hoger Lager 1 oktober 2024 13:43
    CAMBRIDGE, Mass., Oct. 01, 2024 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies, today announced that interim data from the ongoing Phase 1 study of nexiguran ziclumeran (nex-z, also known as NTLA-2001) will be presented in a late-breaking oral presentation at the 2024 American Heart Association (AHA) Scientific Sessions, taking place November 16 – 18 in Chicago, Illinois. Nex-z is an investigational in vivo CRISPR-based gene editing therapy designed to be a single-dose treatment for transthyretin (ATTR) amyloidosis. Intellia leads development and commercialization of nex-z as part of a multi-target discovery, development and commercialization collaboration with Regeneron. The presentation will include safety, reduction in serum TTR and biomarkers of disease progression, and functional capacity data in patients with ATTR amyloidosis with cardiomyopathy (ATTR-CM).

    Presentation Details

    Title: Nexiguran ziclumeran (nex-z, also known as NTLA-2001), an investigational in vivo CRISPR-based therapy for patients with transthyretin amyloidosis with cardiomyopathy (ATTR-CM): interim report of the Phase 1 study

    Session: Late-Breaking Science 1: Celebrating a Century of Cardiovascular Science: From Prevention to Treatment, to Cure

    Session Type: Late-Breaking Science

    Date and Time: Saturday, November 16, 2024, from 8:30-9:45 a.m. CST

    Presenter: Marianna Fontana, M.D., Ph.D., Professor of Cardiology and Honorary Consultant Cardiologist, University College London Centre for Amyloidosis, London, UK

    Location: Main Event I

    About nexiguran ziclumeran (nex-z, also known as NTLA-2001)
    Based on Nobel Prize-winning CRISPR/Cas9 technology, nex-z has the potential to become the first one-time treatment for transthyretin (ATTR) amyloidosis. Nex-z is designed to inactivate the TTR gene that encodes for the transthyretin (TTR) protein. Nex-z is the first investigational CRISPR therapy to be administered systemically to edit genes inside the human body. Interim Phase 1 clinical data showed the administration of nex-z led to consistent, deep and long-lasting TTR reduction. Intellia leads development and commercialization of nex-z as part of a multi-target discovery, development and commercialization collaboration with Regeneron.
  3. Hoger Lager 7 oktober 2024 14:39
    October 7, 2024 7:30 AM EDT
    Intellia Therapeutics Announces Initiation of HAELO Phase 3 Study of NTLA-2002, an Investigational In Vivo CRISPR Gene Editing Treatment for Hereditary Angioedema (HAE)
    NTLA-2002 is a single-dose treatment designed to prevent potentially life-threatening swelling attacks in people with hereditary angioedema (HAE)
    NTLA-2002 is Intellia’s second in vivo candidate to enter late-stage clinical development from its modular gene editing platform
    CAMBRIDGE, Mass., Oct. 07, 2024 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies, today announced the initiation of HAELO, a global, pivotal Phase 3 study of NTLA-2002 for the treatment of hereditary angioedema (HAE). NTLA-2002 is a wholly owned investigational in vivo CRISPR-based gene editing therapy in development as a single-dose treatment for this potentially life-threatening disease. Patient screening is active following Intellia’s successful end-of-Phase 2 meeting and submission of an Investigational New Drug Application amendment to the U.S. Food and Drug Administration (FDA).

    “Initiation of the HAELO Phase 3 trial is a significant milestone for Intellia as we enter the final stage of clinical development for NTLA-2002 for people living with hereditary angioedema,” said Intellia President and Chief Executive Officer John Leonard, M.D. “Data from the ongoing Phase 1/2 study showed great promise that a single-dose treatment can lead to a complete response – no more attacks and no further treatment required. We are working urgently to bring forward NTLA-2002 to address the real-world needs of people suffering from this disease and, ultimately, believe it will bring significant value to patients, physicians and payors.”

    HAELO is a global, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of NTLA-2002 in 60 adults with Type I or Type II HAE. Patients will be randomized 2:1 to receive a single 50 mg infusion of NTLA-2002 or placebo. Patients randomized to the placebo arm will be eligible for optional crossover to NTLA-2002 at week 28. The primary endpoint is the change in number of HAE attacks from week 5 through week 28.

    Intellia is initiating the Phase 3 study based on positive safety and efficacy data from the ongoing Phase 1/2 study (NCT05120830) of NTLA-2002. Interim Phase 1 clinical data showed dramatic reductions in attack rate, as well as consistent, deep and durable reductions in kallikrein levels. Intellia previously announced positive toplines results from the Phase 2 portion of the study. The Company plans to present the detailed results at the 2024 American College of Allergy, Asthma & Immunology (ACAAI) Annual Scientific Meeting, taking place October 24 – 28 in Boston, Massachusetts.
  4. Hoger Lager 7 oktober 2024 16:11
    quote:

    Natal schreef op 7 oktober 2024 16:00:

    Koers lijkt er niks op te doen. De dag is nog jong aan de overkant dus wie weet wat de eindstand zal zijn.
    Biotech heeft flinke klappen gehad de laatste tijd. Misschien zijn mensen toch nog terughoudend. Op termijn gaat dit zeker helpen. De CEO geeft eigenlijk gelijk aan dat de data van fase 2 heel goed is... (die wordt 26 oktober gepresenteerd door Danny Cohn van UMC Amsterdam). Ik wacht rustig af... Maar onder de 20 dollar is een giga kans vind ik. :-)
  5. bodem 10 oktober 2024 10:42
    Das momenteel 40% hoger dan de huidige koers maar met een aandeel als Intellia T. is het uiteindelijk wachten op het eind resultaat dan is die ruime marge snel opgedoekt als en ik zeg als de verwachtingen ingelost kunnen worden.
    Wel vind ik het vervelend dat op 02/10 weer een insider heeft verkocht aan 19$ daar heb ik het lastig mee.
    Succes verder en eerst uitkijken 26/28 -10.
  6. Hoger Lager 10 oktober 2024 22:02
    Dank je. Ik heb ze gekocht voor 2 tot 4 jaar. Ik ben heel blij met deze prijs. Ja, het had achteraf lager gekund maar dat risico nam ik op dat moment.

    Ik denk dat over 2 tot 4 jaar de koers tussen de $50 en $100 staat inclusief minimaal 2 goedkeuringen (ATTR-CM en HAE) En ws ook ATTR-PN. Daarnaast zullen de samenwerkingen ook een stuk verder zijn.
  7. Hoger Lager 11 oktober 2024 15:46
    - Investor webcast to review the NTLA-2002 Phase 2 data is now planned for Thursday, October 24 at 8:30 a.m. ET

    CAMBRIDGE, Mass., Oct. 10, 2024 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies, today announced a new date for its upcoming investor webcast to review the data from the Phase 2 study of NTLA-2002. The webcast will now be held on Thursday, October 24 at 8:30 a.m. ET. The Company had previously announced the investor webcast would be held on on Monday, October 28, 2024.

    There are no changes to the planned oral presentation at the 2024 American College of Allergy, Asthma & Immunology (ACAAI) Annual Scientific Meeting, taking place October 24 – 28 in Boston, Massachusetts.

    To join the webcast, please visit this link, or the Events and Presentations page of the Investors & Media section of the company’s website at www.intelliatx.com. A replay of the webcast will be available on Intellia’s website for at least 30 days following the call.
337 Posts
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