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Aandeel Galapagos AEX:GLPG.NL, BE0003818359

  • 27,180 19 apr 2024 17:35
  • -0,200 (-0,73%) Dagrange 26,860 - 27,280
  • 62.640 Gem. (3M) 81,1K

Galapagos juni 2019

2.736 Posts
Pagina: «« 1 ... 28 29 30 31 32 ... 137 »» | Laatste | Omlaag ↓
  1. forum rang 10 voda 7 juni 2019 22:32
    Beursupdate: AEX op Wall Street

    (ABM FN-Dow Jones) Op Wall Street zijn vrijdag vijf van de negen AEX-genoteerde fondsen ten opzichte van het slot in Amsterdam lager gesloten.

    Aegon (-0,38%)
    ArcelorMittal (+0,51%)
    ASML (-0,18%)
    Galapagos (+3,16%)
    ING Groep (-0,08%)
    Philips (-0,13%)
    RELX (+0,24%)
    Royal Dutch Shell (+0,29%)
    Unilever (-0,11%)

    Euro/dollar: 1,1333

    Op basis van de bovenstaande koersuitslagen zou de AEX index, die sloot op 550,24 punten, zijn geëindigd op 550,45 punten.

    Door: ABM Financial News.
    info@abmfn.nl
    Redactie: +31(0)20 26 28 999

    © Copyright ABM Financial News B.V. All rights reserved.
  2. Beurskingpin 7 juni 2019 23:07
    quote:

    oki cd schreef op 7 juni 2019 20:54:

    Lang geleden dat Gala usa argen-x voorbij ging
    Bent u nu de koers van gala aan het vergelijken met de koers van argenx zoals de kindjes dit doen? De koers zegt niets over de marktkapitalisatie, het zijn de uitstaande aandelen die tellen..
  3. royal cancun 8 juni 2019 02:37
    quote:

    DeHardeWerker schreef op 7 juni 2019 19:20:

    [...]

    Hoeveel verzoeken zijn er richting moderator gegaan met verzoek om een einde te maken aan je dagelijkse geklaag, gehuil en gejammer op de diverse fora ? Lees even het bericht van gisteravond terug van jan941 op 6 jun 2019, 17:32 en de reacties daarop (41 likes(!!!)). Maar je blijft maar doorgaan met klagen en roeptoeteren! Je zult versteld staan van de positieve reacties die je krijgt als je daar eens iets aan doet.

    Naast je eeuwige geklaag, gehuil en gejammer zie ik eigenlijk geen enkele inhoudelijke bijdrage van jou, of bedoel je het knip- en plakwerk van de analyses van Nico Bakker, waarbij je net doet alsof je die zelf bedacht hebt ?
    Kom je soms thuis niet aan je trekken om je frustraties af te reageren op mm.
  4. [verwijderd] 8 juni 2019 08:28
    Deal tussen VS en Mexico, heffingen opgeschort

    Vandaag 08:01,
    WASHINGTON (AFN) - De Verenigde Staten en Mexico hebben een deal bereikt over de aanpak van illegale immigratie. De handelstarieven die de VS wilden opleggen zijn daardoor van de baan. Dat meldt de Amerikaanse president Donald Trump op Twitter.
  5. Beurskingpin 8 juni 2019 11:20
    quote:

    oki cd schreef op 8 juni 2019 10:52:

    [...]
    Dank voor deze volwassen reactie.
    In ieder geval volwassener dan de eeuwige vergelijking tussen gala en argenx op basis van de koers van het aandeel ipv de vergelijking tussen de marktkapitalisatie van beiden. Is net hetzelfde als ik zou zeggen dat galapagoskoers hoger staat dan die van gilead.. lekker belangrijk seg..
  6. robbie123 8 juni 2019 12:02
    quote:

    amston schreef op 8 juni 2019 10:47:

    Nog 3 wk en dan 3e kwart ....

    EU/MAA submission for RA !!!!
    -------------------------------------------

    Gilead: pag.52 Q1-2019 pipeline

    Blijft de vraag: juli of september...
    Beste Amston
    Inflammation passages in deze link lezen dan krijg je een globaal idee lijkt me

    seekingalpha.com/article/4268488?sour...
  7. E Green 8 juni 2019 13:10
    Efficacy and Safety of Filgotinib for Patients with Rheumatoid Arthritis with Inadequate Response to Methotrexate: FINCH1 Primary Outcome Results (oral #LB0001; 16.25 CET, 12 juni, Hall 6)
    Efficacy and Safety of Filgotinib for Patients with Rheumatoid Arthritis Naïve to Methotrexate Therapy: FINCH3 Primary Outcome Results (oral #LB0003; 8.00 CET, 15 juni, Hall 7B) benieuwd
  8. BLOO7 8 juni 2019 13:38
    quote:

    amston schreef op 8 juni 2019 10:47:

    Nog 3 wk en dan 3e kwart ....

    EU/MAA submission for RA !!!!
    -------------------------------------------

    Gilead: pag.52 Q1-2019 pipeline

    Blijft de vraag: juli of september...
    investors.gilead.com/static-files/ead...

    Kwartaal 3 reeds, dat is vlug.
    Er zit vaart achter.
    Kwartaal 3 valt ook in H2. ;-)
  9. BLOO7 8 juni 2019 14:05
    quote:

    amston schreef op 8 juni 2019 13:57:

    Ja dat weet ik ook wel...
    Maar het gaat nu om: of 3e kwartaal. Of 2e half jaar.....
    Kan max. 6 maanden verschil uitmaken !!

    Houd het maar op Q3, maar O'Day wil natuurlijk niet dat de Galapagos koers ontploft, hij wil Galapagos betaalbaar houden.
    Al kon hij zijn enthousiasme niet onderdrukken op Jefferies:

    Opgelijnd:
    The second priority is really looking at the commercial delivery. But really getting my arms around the commercial delivery of the company and getting ready for filgotinib for instance in inflammation which is an important new area for us.
    Sure. So I think I mean first of all, I think filgotinib has a very attractive competitive profile. I mean let's face it. It's been highly successful in three different patient populations at two doses. And we've seen good effect and good safety profile of both of those doses in the JAK class. So I think first and foremost in a field that is looking for options for patients first in RA and then potentially in IDB and other indications that we obviously have a lot of work going on. That is an area that is -- has unmet medical needs around highly efficacious, highly safe and convenient drugs for patients. Patients who are not yet well managed in the field of rheumatoid arthritis for instance and we've got lots of that we could do in terms of [indiscernible] CR58 or 70 responses so they are much higher than we have today.
    So filgotinib, I think in and of itself is a very competitive product profile and something we now have to build up to be successful in the commercial launch here. Having some experience in this and my past we really got to ramp up now to be successful there
    Sure. No. I think look, I think we have to be eyes wide open going into this market. It's got a lot of options of course. And yet I don't think it's yet well served from the standpoint of a convenient or highly efficacious medicine that's safe. So at the end of the day, first and foremost, it's about the product profile. And I think we have the 24. We have the 24-week data now. We'll have the 52-week data shortly and assuming that's all confirmed. And we have a strong path forward there. I think the product profile even being a little bit later to the JAK game can certainly play effectively. Of course, we have to be smart about how we do that. It's still in most markets particularly around the world of specialty driven markets. So I think Gilead can be successful and has been successful on specialty driven market that some backbone infrastructure that we can leverage.
    And then, of course, there's a need for bringing on expertise that will be specific in the medical and sales area for the JAK class. I would say as we go into IDB and those trials still need to read out. It's a slightly different competitive profile where we have the chance to be potentially second and some indications with IDB depending on the data. So, our order of entry also will move up potentially in IDB and that's still quite an untapped market. So you have to look at the totality of the lifecycle management I think of the JAK with a good strong launch.
    Right. I think the overall safety profile has been well demonstrated now in the three trials associated with three different disease states. And we have a clear path forward for Europe. We'll be filing there towards the second half of this year and in the U.S., we think we have a very good -- now with the totality of data it will be the first time and we'll be dialoguing with the FDA in the near term to talk about the totality of the data set, right? So, the entirety of the safety profile associated with the efficacy that we're seeing across different doses and different treatment paradigms and come back to you in the second half of this year with the outcome of those discussions. But we remain optimistic and confident about the path forward also in the U.S.
    So, yes, I think with any medicine and any discussion with the regulator, you have to look at the benefit risk profile in totality. And I think in my experience that's the way, the FDA has always looked at medicines and products and so we need to have that discussion. But yes, I do think one needs to look at the total benefit of that product and put certain early preclinical signals into context.
2.736 Posts
Pagina: «« 1 ... 28 29 30 31 32 ... 137 »» | Laatste |Omhoog ↑

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