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Aandeel Galapagos AEX:GLPG.NL, BE0003818359

Laatste koers (eur) Verschil Volume
23,180   +0,100   (+0,43%) Dagrange 22,900 - 23,420 106.827   Gem. (3M) 112K

Galapagos mei 2020

4.897 Posts
Pagina: «« 1 ... 37 38 39 40 41 ... 245 »» | Laatste | Omlaag ↓
  1. durobinet 7 mei 2020 19:23
    Gilead confirms remdesivir approval in Japan for severe COVID-19
    May 7, 2020 11:52 AM ET|About: Gilead Sciences, Inc. (GILD)|By: Douglas W. House, SA News Editor
    Under exceptional (emergency use) status, Japan's Ministry of Health, Labor and Welfare has approved Gilead Sciences' (GILD +0.4%) remdesivir, branded as Veklury, for the treatment of severely ill COVID-19 patients.
  2. forum rang 4 Raasgier 7 mei 2020 22:03
    Our revenues and other income for the first three months of 2020 amounted to €106.9 million, compared to
    €40.9 million for the first three months of 2019. Revenues (€98.2 million for the first three months of 2020
    compared to €33.0 million for the first three months of 2019) were higher due to the revenue recognition of the
    upfront payment received from Gilead in August 2019 related to (i) the exclusive access to our drug discovery
    platform during the collaboration period and exclusive option rights on our current and future clinical programs
    after Phase 2 outside Europe, and (ii) additional consideration received for the extended cost sharing for filgotinib.
    Other income (€8.7 million vs €7.9 million for the same period last year) increased, mainly driven by higher
    incentives income from the government for our R&D activities.
  3. forum rang 4 Raasgier 7 mei 2020 22:06
    With regard to Toledo, our novel mode of action program in inflammation, we completed Phase 1 studies
    in healthy volunteers with our Toledo drug candidates, GLPG3312 and GLPG3970. Given the superior profile of
    GLPG3970 observed in Phase 1, we decided to prioritize the further development of GLPG3970. We still anticipate
    the start of several proof-of-concept patient trials with GLPG3970 in the second half of the year, with topline
    results now expected in the first half of 2021.
  4. forum rang 4 Raasgier 7 mei 2020 22:07
    Ok, dit even niet hardop zeggen:

    From a financial perspective, we ended the first quarter of 2020 with a cash position of €5.7 billion which will allow
    us to grow our pipeline and attract new talent to support our ambitious growth plan. As a result of COVID-19, our
    cash burn guidance for FY2020 is expected to be in the range of €400 - €430 million, down versus the previously
    stated cash burn projection due to the pause in recruitment or postponed starts of some clinical trials
  5. forum rang 4 Raasgier 7 mei 2020 22:10
    The FDA has confirmed priority review with a PDUFA goal date in the second half of this year. As with all
    applications, but particularly during these difficult circumstances, potential approval timings are subject
    to change --> Dus niet per se eerder dan de beredeneerde 19 augustus. Al zit je dan wel al zes weken in H2, dus het hoeft ook niet per se later.
  6. Jan87 7 mei 2020 22:13
    Ik heb vragen bij dit stukje:

    Voor Toledo, ons nieuw mode of action programma in ontsteking, hebben we de Fase 1-studies van onze Toledo kandidaatmedicijnen GLPG3312 en GLPG3970 in gezonde vrijwilligers afgerond. Gezien het superieure profiel van GLPG3970 waargenomen in Fase 1, hebben we besloten om prioriteit te geven aan de verdere ontwikkeling van deze compound. Uitgaande van positieve ontwikkelingen met betrekking tot de COVID-19-pandemie verwachten we om in de tweede helft van het jaar meerdere proof-of-concept-studies bij patiënten op te starten met GLPG3970. De topline resultaten worden nu verwacht in de eerste helft van 2021.

    Hoezo superieur profiel in Fase 1 van 3970 ? Hebben we toch geen PB van gezien of mis ik iets ?
  7. forum rang 4 Raasgier 7 mei 2020 22:13
    quote:

    Mippert schreef op 7 mei 2020 22:08:

    GOED toch?

    Morgen -/- 10% ?
    Ik lees alleen goede dingen, maar dat is een zeer oppervlakkige scan van 5 minuten. En de voortgang van de studies waag ik me even niet aan, dat hebben anderen scherper op hun radar. Maar het woordje 'vertraging' komt er niet veel in voor. Sterker nog, zoeken op het woordje 'delay' geeft precies 1 hiet:

    Due to the temporary pause in recruitment for a number of ongoing Phase 2 and 3 trials and delays in the start
    of a number of planned early-stage trials, our cash burn guidance has been revised down and is now expected to
    be in the range of €400 and €430 million compared to €420 and €450 million previously guided. The cash burn
    includes milestone income from Gilead for potential regulatory approvals of filgotinib in RA.

    En die info hadden we al, geloof ik toch.

    Over die 10% durf ik verder lekker ook niks te zeggen. Nu even socializen met mw Raasgier. Goedenavond allen.
4.897 Posts
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