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Aandeel Galapagos AEX:GLPG.NL, BE0003818359

Laatste koers (eur) Verschil Volume
24,780   -0,040   (-0,16%) Dagrange 24,140 - 25,000 126.607   Gem. (3M) 109,1K

Galapagos december 2016

1.359 Posts
Pagina: «« 1 ... 20 21 22 23 24 ... 68 »» | Laatste | Omlaag ↓
  1. [verwijderd] 13 december 2016 19:56
    Vorig jaar de aankondiging 'Nieuwjaarsborrel' voor het tekenen van de Filgotinib deal.
    Gaat dit jaar SAPHIRA 1 het verdere uitstekend verlopen jaar 2016 voor Galapagos wederom perfect doen afsluiten....

    Studie SAPHIRA 1 d.d. 6 december 2016 'completed', zoals hier reeds gemeld.
    Zeer benieuwd naar de scores. Commercieel een kans voor Galapagos om patienten klasse III CF te helpen met beter medicijn dan Kalydeco.

    Het aantal nachten tot aan publicatie van SAPHIRA 1 is idd. beperkt Medion:).

    Exciting times @Galapagos.
  2. egeltjemetstekel 13 december 2016 19:56
    quote:

    Chicken . Jazeker wel! schreef op 13 december 2016 19:52:

    [...]
    er is altijd nog de twitterfeed

    twitter.com/BioStockAddict

    BioStockAddict ?@BioStockAddict
    I even have a Chicken following me now.
    At some places he is known as a $GLPG contra-indicator Chicken. LOL
  3. [verwijderd] 13 december 2016 20:15
    quote:

    egeltjemetstekel schreef op 13 december 2016 19:52:

    [...]is dat soms voor jou de reden geweest ons landje te verlaten?
    Nee. Het werd mij te zwart waar ik woonde.

    Het was mooi groen, maar asfalt nam hand over hand toe, en ik voorzag geen einde aan de urbanisatie.

    En er waren nog een paar redenen die meer hout sneden ;)
  4. pardon 13 december 2016 20:17
    About the SAPHIRA Phase 2 program

    SAPHIRA 1, an open-label study of three doses of GLPG1837 in at least 12 patients with the G551D mutation, was first dosed in patients this week. SAPHIRA 2, an open-label study of two doses of GLPG1837 in at least six CF patients with the S1251N mutation, was first dosed in February 2016. The SAPHIRA Phase 2 program will explore the safety, tolerability, efficacy, and medicine-like properties of GLPG1837 in patients in six EU countries and Australia. Primary objectives are to evaluate the safety and tolerability; secondary objectives are to assess changes in sweat chloride from baseline as the biomarker of cystic fibrosis transmembrane conductance regulator (CFTR) ion channel function and to explore the changes in pulmonary function (forced expiratory volume in 1 second [FEV1]) from baseline. Both studies will include subjects treated with Kalydeco®1 as well as those who are naïve to this drug. In each study, different doses of GLPG1837 tablets will be administered twice daily for a total duration of four weeks. Both SAPHIRA studies are recruiting on track with plan.

    About the Galapagos-AbbVie collaboration in cystic fibrosis

    In September 2013 Galapagos and AbbVie, a global biopharmaceutical company, entered into a global collaboration agreement focused on the discovery and worldwide development and commercialization of potentiator and corrector molecules in a potential triple combination therapy for the treatment of CF. Under the terms of the agreement, AbbVie made an upfront payment of $45 million to Galapagos. Upon successful completion by Galapagos of clinical development through to completion of Phase 2, AbbVie will be responsible for Phase 3, with financial contribution by Galapagos. Galapagos has received an additional $20 million in payments from AbbVie to date and is eligible to receive up to $340 million in total additional payments for developmental and regulatory milestones, sales milestones upon the achievement of minimum annual net sales thresholds an
  5. [verwijderd] 13 december 2016 22:05
    quote:

    pardon schreef op 13 december 2016 17:34:

    Gilead dividend en bijna 2 $ hoger vandaag.

    In March, the company shuttered a half dozen trials seeking to expand the use of its cancer drug Zydelig. Since then, Gilead Sciences has stopped development of GS-5745 for ulcetrative colitis and Crohn's disease, and reported disappointing results for its cardiovascular drug GS-6615. Recently, results for the NASH (a liver disease) drug GS-4997 failed to impress industry watchers, too.

    Given Gilead Sciences' top line was 10% smaller in the third quarter than a year ago, the company could use a win. Unfortunately, that win isn't likely to be momelotinib.

    Fails to outperform
    Results from two momelotinib phase 3 trials were reported, and neither of them delivered data that's likely to reshape how doctors treat myelofibrosis patients.

    In Gilead Sciences' Simplify-1 study, momelotinib was statistically non-inferior to Jakafi in reducing spleen volume, with 26.5% of momelotinib patients and 29% of Jakafi patients achieving at least a 35% reduction. However, non-inferiority was not achieved for the secondary endpoint of response rate in total symptom score.

    In the Simplify-2 study, momelotinib failed to meet its primary endpoint in a study evaluating its superiority to best alternative therapy, which in most cases was Jakafi.

    Gilead Sciences' chief scientific officer, Norbert Bischofberger, attempted to put a positive spin on the results by highlighting some improvements in anemia-related secondary endpoints, but Bischofberger's attempts add little confidence that momelotinib has any chance of displacing Jakafi in the indication. "The results from both the SIMPLIFY-1 and SIMPLIFY-2 studies indicate that momelotinib provides some treatment benefit, including benefit on anemia-related endpoints," said Bischofberger, adding, "We plan to discuss these results with regulatory authorities to determine the next steps."

    Maintaining its lead
    Incyte's twice-daily Jakafi won FDA approval for use in myelofibrosis patients in 2011 and notched an FDA green light in polycythemia vera -- another bone marrow disease -- in 2014. Sales of Jakafi have been building ever since.

    In Q3, Jakafi's sales of $224 million were 39% higher than in the same quarter last year; and earlier this month, management said Jakafi's sales would be between $850 million and $855 million this year. In 2015, Jakafi's sales were $601 million. In the past year, the numbers of myelofibrosis patients and polycythemia vera patients taking Jakafi have increased by roughly 20% and 40%, respectively.

    G

    IMAGE SOURCE: INCYTE CORPORATION.

    Given momelotinib's performance, it's unlikely Jakafi's position in the indication is in jeopardy, and that adds important clarity to Incyte's sales potential for 2017.

    Eyes on the future
    Gilead Sciences still has some promising candidates in development, including filgotinib, an autoimmune disease treatment that's in phase 3 studies. Pressure, however, is mounting for Gilead Sciences to deliver some R&D wins, or to deploy its massive cash stockpile to buy future growth. So far, Gilead Sciences' management has been coy about its acquisition plans, but it has indicated the company remains interested in expanding in oncology. Perhaps momelotinib's results mean that Incyte has become an attractive target. Regardless, it appears Jakafi's market share will remain intact, at least for now, and that's good news for Incyte investors.
    Whats the problem, they got a deal with Galapagos with Filgotinib...
  6. egeltjemetstekel 13 december 2016 23:04
    quote:

    keerputbever schreef op 13 december 2016 22:48:

    [...]

    Zelfs meester Henk vond het verhaaltje van Kelewan niet zo goed.
    Dus je wilt Meester henk graag pleasen?
    Nou dan kun je het beste nu nog geen januari draadje openen.
    En of jij de juiste persoon daarvoor bent is een andere vraag...
    Mij maakt het niks uit.
  7. [verwijderd] 14 december 2016 09:03
    Beursblik: KBC Securities lanceert favorietenlijst 2017

    In 2016 ruim 9 procent winst.

    (ABM FN) KBC Securities heeft tien aandelen geselecteerd voor 2017, namelijk AB InBev, Aedifica, Ahold Delhaize, Econocom, GALAPAGOS!!, NN Group, Orange Belgium, Refresco, SBM Offshore en TKH Group.

    "Een uitgebalanceerde lijst met enkele cyclische en meer defensieve namen", aldus de analisten van het Belgische beurshuis.

    De favorietenlijst van KBC Securities behaalde in 2016 vooralsnog een winst van iets meer dan 9 procent, waarmee zowel de Bel20 als de Euro STOXX 50 werd verslagen. De AEX presteerde evenwel beter dan de selectie van het beurshuis. Aanjagers in de favorietenlijst waren dit jaar onder meer Umicore (+49,5%), Melexis (+42,0%) en SBM Offshore (+18,2%). Tegenvallers waren bijvoorbeeld Randstad (-8,1%), BAM Groep (-10,0%) en vooral Grandvision (-20,0%).

    Ook selecteerde KBC Securities een vijftal kleine aandelen die het komend jaar goed zouden moeten presteren. Naast het Nederlandse Beter Bed staan het Belgische Biocartis, Immobel, Nyrstar en Recticel op de lijst.

    Door: ABM Financial News.
  8. Loureiro 14 december 2016 09:17
    GLPG ontving afgelopen maand 70 miljoen $ mijlpaalbetalingen zonder koersreactie! Niet te begrijpen.
    Het is nu wachten op resultaten Saphira2.
    Bij goede resultaten zou de koers wel eens serieus kunnen stijgen boven de 60 euro omdat de kansen groter worden dat er naast Filgotinib (Gilead) ook een medicijn aankomt in samenwerking met Abbvie.
    Het worden spannende tijden.
1.359 Posts
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