Ontvang nu dagelijks onze kooptips!

word abonnee
IEX 25 jaar
Uitgebreid zoeken

Beurscodes, betekenis en hulp bij zoeken

Europa

AEX
Euronext Amsterdam
BRU
Euronext Brussels
PSE
Euronext Paris
LIS
Euronext Lissabon
CHX
CBOE Europe, grote(re) EU aandelen
NAV
Investment Funds (NAV)

Noord-Amerika

NYS
New York Stock Exchange
OTC
CBOE BZX Exchange (US)
TSE
Toronto Stock Exchange

Kunt u een instrument niet vinden?

Zoek dan via de zogenaamde ISIN code. Elk instrument, aandeel etc. heeft een unieke code.

Kies vervolgens - wanneer er meerdere resultaten zijn - de notering op de beurs van uw keuze.

Waar vind ik die ISIN code?

Google de naam van het instrument, aandeel etc. met de toevoeging 'ISIN'.

Als zoeken op ISIN code geen resultaten oplevert hebben wij het instrument of aandeel niet in onze koersendatabase.

desktop iconMarkt Monitor
Markt vandaag Koersen Forum Premium IEX Expert
Home  /   Forum   /   arGEN-X   /   ARGEN-X 2019 De nieuwe parel !

Aandeel arGEN-X BRU:ARGX.BL, NL0010832176

Laatste koers (eur) Verschil Volume
558,200   +3,800   (+0,69%) Dagrange 554,400 - 565,200 22.667   Gem. (3M) 50,2K

ARGEN-X 2019 De nieuwe parel !

Volgen
1.115 Posts
Pagina: «« 1 ... 49 50 51 52 53 ... 56 »» | Laatste | Omlaag ↓
  6. Stafke 10 december 2019 22:17
    argenx announces publication of efgartigimod Phase 2 primary immune thrombocytopenia trial results in American Journal of Hematology

    Efgartigimod was well-tolerated and showed a correlation of reduced IgG levels, increased platelet counts and reduced bleeding in ITP patients

    December 10, 2019

    Breda, the Netherlands / Ghent, Belgium – argenx (Euronext & Nasdaq: ARGX), a clinical-stage biotechnology company developing a deep pipeline of differentiated antibody-based therapies for the treatment of severe autoimmune diseases and cancer, today announced the publication of results from the completed Phase 2 clinical trial of its FcRn antagonist, efgartigimod, in adult patients with primary immune thrombocytopenia (ITP) in the American Journal of Hematology. The peer-reviewed article is titled, “Phase 2 study of efgartigimod, a novel FcRn antagonist, in adult patients with primary immune thrombocytopenia,” and can be accessed here.

    “We are pleased to have this publication of the full Phase 2 ITP trial results available to the hematology community, highlighting the novel approach of efgartigimod as a new treatment modality in ITP. Patients continue to need additional therapeutic options for this difficult-to-treat disease. Efgartigimod has demonstrated a favorable tolerability profile and the ability to drive encouraging response rates in a refractory population after a limited exposure. We now look forward to advancing efgartigimod into a global Phase 3 program in ITP before the end of 2019 where we have the opportunity to dose in a longer-term setting,” said Wim Parys, M.D., chief medical officer of argenx.

    The Phase 3 program of efgartigimod in ITP remains on track to initiate this month and will evaluate the intravenous (IV) formulation in the first clinical trial, ADVANCE, and an IV induction followed by a subcutaneous (SC) maintenance injection in the second clinical trial, ADVANCE SC.

    In addition to ITP, efgartigimod is currently being evaluated as a treatment for other severe autoimmune diseases, including generalized myasthenia gravis (gMG), pemphigus vulgaris (PV), and chronic inflammatory demyelinating polyneuropathy (CIDP). The Phase 3 ADAPT trial of IV efgartigimod is ongoing in gMG with data expected in the second half of 2020. A Phase 2 proof-of-concept trial of IV efgartigimod is ongoing in PV and data are expected in the first half of 2020. A Phase 2 proof-of-concept trial of SC efgartigimod in CIDP is expected to start before the end of 2019.

    About efgartigimod

    Efgartigimod is an IgG Fc fragment engineered to optimally antagonize the neonatal Fc Receptor (FcRn) for the treatment of IgG-mediated autoimmune diseases. FcRn plays a central role in rescuing IgG from degradation in the lysosome through a recycling pathway. Through inhibition of FcRn, efgartigimod leads to fast depletion of the disease-causing IgG autoantibodies. Efgartigimod binds in the same way as endogenous IgG, the natural ligand of FcRn, and has been engineered with ABDEG™ mutations to increase its affinity for FcRn while preserving the characteristic pH-dependent binding, contributing to its long serum half-life, pharmacodynamic effect and potentially enhanced tissue penetration. The development work on efgartigimod is conducted in close collaboration with Prof. E. Sally Ward (Department of Molecular and Cellular Medicine, Texas A&M University Health Science Center, College Station, TX; Center for Cancer Immunology, University of Southampton, Southampton, UK).

    About argenx
    argenx is a clinical-stage biotechnology company developing a deep pipeline of differentiated antibody-based therapies for the treatment of severe autoimmune diseases and cancer. The company is focused on developing product candidates with the potential to be either first-in-class against novel targets or best-in-class against known, but complex, targets in order to treat diseases with a significant unmet medical need. argenx’s ability to execute on this focus is enabled by its suite of differentiated technologies. The SIMPLE AntibodyTM Platform, based on the powerful llama immune system, allows argenx to exploit novel and complex targets, and its three complementary Fc engineering technologies are designed to expand the therapeutic index of its product candidates.

    For further information, please contact:

    Beth DelGiacco, Vice President, Investor Relations
    +1 518 424 4980
    bdelgiacco@argenx.com

    Joke Comijn, Director Corporate Communications & Investor Relations (EU)
    +32 (0)477 77 29 44
    +32 (0)9 310 34 19
    info@argenx.com

    Forward-looking Statements

    The contents of this announcement include statements that are, or may be deemed to be, “forward-looking statements.” These forward-looking statements can be identified by the use of forward-looking terminology, including the terms “believes,” “estimates,” “anticipates,” “expects,” “intends,” “may,” “will,” or “should” and include statements argenx makes concerning future clinical trial design, timelines and data availability and the intended results of its strategy. By their nature, forward-looking statements involve risks and uncertainties and readers are cautioned that any such forward-looking statements are not guarantees of future performance. argenx’s actual results may differ materially from those predicted by the forward-looking statements as a result of various important factors, including argenx’s expectations regarding its the inherent uncertainties associated with competitive developments, preclinical and clinical trial and product development activities and regulatory approval requirements; argenx’s reliance on collaborations with third parties; estimating the commercial potential of argenx’s product candidates; argenx’s ability to obtain and maintain protection of intellectual property for its technologies and drugs; argenx’s limited operating history; and argenx’s ability to obtain additional funding for operations and to complete the development and commercialization of its product candidates. A further list and description of these risks, uncertainties and other risks can be found in argenx’s U.S. Securities and Exchange Commission (SEC) filings and reports, including in argenx’s most recent annual report on Form 20-F filed with the SEC as well as subsequent filings and reports filed by argenx with the SEC. Given these uncertainties, the reader is advised not to place any undue reliance on such forward-looking statements. These forward-looking statements speak only as of the date of publication of this document. argenx undertakes no obligation to publicly update or revise the information in this press release, including any forward-looking statements, except as may be required by law.

    This messsage was distributed by Nasdaq's GlobeNewswire.
    (165 Broadway, New York, NY, 10006, USA, 1.212.401.8700, www.nasdaq.com)
    On behalf of argenx SE Willemstraat 5, Breda, 4811 AH NL
  9. dany 1964 11 december 2019 07:16
    (ABM FN) Argen-X heeft de resultaten van de fase II studie met efgartigimod voor de behandeling van primaire immuunstrombocytopenie in de American Journal of Hematology gepubliceerd. Dit maakte het Belgische biotechbedrijf dinsdagavond bekend.
    “We zijn blij met deze publicatie van de volledige Fase 2 ITP onderzoeksresultaten”, aldus Chief Medical Officer Wim Parys van Argen-X in een toelichting.
    Efgartigimod wordt volgens Argen-X goed verdragen en laat een goede reactie zien na een beperkte blootstelling, aldus Parys
    “Wij verheugen ons nu op de volgende stap met efgartigimod in een mondiaal Fase III programma in ITP vóór het einde van 2019”, voegde hij toe.
    op naar de 150
  14. [verwijderd] 11 december 2019 12:33
    quote:

    TP66 schreef op 11 december 2019 09:17:

    KBC koersdoel 9 december 130 euro, op 11 december een koersdoel afgegeven van 159 euro.

    Ik begin steeds meer mijn twijfels te krijgen over hun kennis en vaardigheden of ze wel de kwaliteiten hebben om goede analyses te maken??
    de koersdoelen van KBC zijn ronduit belachelijk; ze lopen ook altijd de koers achterna

    ik moet wel toegeven dat ik de 140 niet zo snel had verwacht
  17. forum rang 4 Jan66 12 december 2019 08:05
    quote:

    Elvisfan schreef op 11 december 2019 17:29:

    [...]

    ja, wil ik best geloven, maar het grote nieuws is pas voor de 2de helft 2020 .... mss loopt de koers wat vooruit op t hetgeen moet komen
    Dat zou zo maar kunnen maar Argenx word steeds meer genoemd in de favoriete lijstjes van de diverse analisten.
  19. forum rang 4 Jan66 12 december 2019 10:08
    quote:

    Sweetheart schreef op 12 december 2019 09:27:

    Het is in ieder geval zo dat je er beter heel stevig kunt inzitten wanneer de Phase 3 resultaten van argx113 volgende jaar bekendgeraken.

    Je moet dan wel het risiko nemen dat de resultaten goed gaan zijn en dat is zeker niet altijd het geval.
    Het blijft inderdaad een risico aandeel.
  20. forum rang 6 de tuinman 12 december 2019 22:37
    quote:

    Sweetheart schreef op 12 december 2019 09:27:

    Het is in ieder geval zo dat je er beter heel stevig kunt inzitten wanneer de Phase 3 resultaten van argx113 volgende jaar bekendgeraken.

    Je moet dan wel het risiko nemen dat de resultaten goed gaan zijn en dat is zeker niet altijd het geval.
    Wel meerdere poc resultaten. Dat geeft mij wel vertrouwen. Zoals bv werking en veiligheid.
1.115 Posts
Pagina: «« 1 ... 49 50 51 52 53 ... 56 »» | Laatste |Omhoog ↑

Meedoen aan de discussie?

Word nu gratis lid of log in met je emailadres en wachtwoord.

Direct naar Forum

Premium drie voorbeelden van IEX Premium: de exclusieve content op de site, de app op een smartphone en IEX Magazine.

Benieuwd naar onze analyses en kooptips?

Word nu abonnee van IEX en krijg onbeperkt toegang tot onze (koop)tips en succesvolle modelportefeuilles. Nu 3 maanden voor slechts €19,95! Profiteer van 58% korting!

Word abonnee

arGEN-X Nieuws

  1. Argenx benoemt bestuurslid
  2. Zes nieuwe namen op favorietenlijst KBC
  3. Beursblik: bedrijfswinsten dalen 20 procent
  4. Argenx krijgt groen licht FDA