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Aandeel Pharming Group AEX:PHARM.NL, NL0010391025

Laatste koers (eur) Verschil Volume
0,738   -0,020   (-2,57%) Dagrange 0,736 - 0,763 3.727.215   Gem. (3M) 4,8M

Pharming Augustus 2020

10.441 Posts
Pagina: «« 1 ... 80 81 82 83 84 ... 523 »» | Laatste | Omlaag ↓
  1. [verwijderd] 6 augustus 2020 15:32
    INTELLIA EXPECTS IND FOR HAE DRUG IN H2 OF 2021

    From Intellia Therapeutics, Inc.’s presentation of the financial results for the second quarter of 2020:

    NTLA-2002 is a wholly owned, in vivo development candidate for the treatment of HAE. Building on Intellia’s modular lipid nanoparticle (LNP) delivery system, NTLA-2002 is designed to knock out the prekallikrein B1 (KLKB1) gene in the liver after a single course of treatment, which is expected to prevent improperly regulated bradykinin production and therefore, reduce HAE attacks.

    In a non-human primate (NHP) study of its lead LNP formulation for NTLA-2002, the knockout of KLKB1 resulted in a therapeutically relevant reduction of serum kallikrein levels and activity following a single dose. Consistent with the durability achieved in earlier NHP studies for its lead in vivo program, Intellia has now demonstrated sustained kallikrein activity reduction for 10 months in an ongoing study. Based on these results, Intellia believes NTLA-2002 could be efficacious and durable in preventing HAE attacks following a single course of treatment.

    Intellia continues to progress IND-enabling (Investigational New Drug) activities and is on track to submit an IND or IND-equivalent for NTLA-2002 in the second half of 2021.
    (Source: Intellia)
  2. [verwijderd] 6 augustus 2020 15:34
    BIOCRYST WILL LAUNCH ITS FIRST ORAL HAE DRUG THIS YEAR

    “We are currently in an exciting transformation from a company primarily focused on R&D to one that is about to launch its first oral drug to patients with HAE (ORLADEYO) this year. We expect to end the year with ORLADEYO approved in the U.S. and Japan”, says President and CEO Jon Stonehouse, BioCryst Pharmaceuticals, Inc., at the presentation of the financial results for the second quarter of 2020.

    HAE Program – ORLADEYO: Oral, once-daily treatment for prevention of HAE attacks

    BioCryst expects three regulatory approvals for ORLADEYO in Q4 2020 and early 2021.
    The U.S. Food and Drug Administration (FDA) is reviewing a new drug application for ORLADEYO and has set an action date of 3 December 2020, under the Prescription Drug User Fee Act (PDUFA).
    In Japan, ORLADEYO is being reviewed under Sakigake designation. The Pharmaceutical and Medical Devices Agency (PMDA) has confirmed their regulatory review schedule and the company expects an approval decision in December 2020.
    On 30 March 2020, the company announced that the European Medicines Agency (EMA) had validated its marketing authorization application (MAA) submission for ORLADEYO and begun its formal review of the MAA under the centralized procedure. The company expects an opinion from the Committee for Medicinal Products for Human Use (CHMP) within approximately 12 months from MAA validation.
    BioCryst has completed significant preparations to support the launch of ORLADEYO in the U.S.
    The company has attracted an accomplished U.S. rare disease sales team, which averages 20 years in pharmaceutical sales and nearly a decade of rare disease experience.
    The company is well-positioned in terms of product supply and inventory on-hand to support the launch and anticipated global demand for ORLADEYO.
    On 9 June 2020, the company announced that it had established an expanded access program with ORLADEYO for patients with HAE in the United States. Through this program, physicians may be able to request ORLADEYO for HAE patients who do not have access to the product through a clinical trial.
    On 6 June 2020, at the European Academy of Allergy and Clinical Immunology (EAACI) Digital Congress, the company presented new data highlighting the burden of therapy faced by HAE patients taking currently available injectable prophylactic medication. Patients taking oral, once daily ORLADEYO experienced sustained decreases in their attack frequency and improvements in quality of life scores over 48 weeks. ORLADEYO was also safe and generally well-tolerated over 48 weeks in both the APeX-2 and APeX-S clinical trials.
    “Our ongoing dialogue and research with HAE patients and physicians continue to reinforce their strong demand for an oral, once-daily medicine that is safe and provides the significant and sustained attack reduction we are seeing with ORLADEYO in our clinical program. Nearly half of patients in our APeX-2 and APeX-S trials have prior experience with injectable or infused therapies and most have chosen to remain on ORLADEYO,” said Charlie Gayer, chief commercial officer of BioCryst.
    (Source: BioCryst)
  3. forum rang 10 voda 6 augustus 2020 15:47
    quote:

    DeepSpaceHorizon schreef op 6 augustus 2020 15:46:

    Ik kan ook wel 10000 berichten plaatsen over net zo veel bedrijven... Maar wat is hier nu de bedoeling van? Plaats het dan in het sector nieuws draadje... Blijft het iets overzichtelijker.
    Ik heb dat ook al eens eerder gezegd. Hij trekt zich toch van niemand wat aan.
  4. forum rang 4 Drieklezoor 6 augustus 2020 15:54
    De penny-stock liefhebbers regeren met ijzeren vuist , een beetje lucht erin en een beetje lucht eruit .Het lijkt wel een opdracht !! eerst moet de emotionele lucht er uit , en een positief bericht en de lucht klaart weer positief op, met dit berichtje los ik niet de problemen op , maar hoopt de twijfelaars hun aandelen niet te verkopen.
  5. forum rang 6 De amateur 6 augustus 2020 16:17
    quote:

    De Monitor - De Pharming Expert schreef op 6 augustus 2020 15:34:

    BIOCRYST WILL LAUNCH ITS FIRST ORAL HAE DRUG THIS YEAR

    “We are currently in an exciting transformation from a company primarily focused on R&D to one that is about to launch its first oral drug to patients with HAE (ORLADEYO) this year. We expect to end the year with ORLADEYO approved in the U.S. and Japan”, says President and CEO Jon Stonehouse, BioCryst Pharmaceuticals, Inc., at the presentation of the financial results for the second quarter of 2020.

    HAE Program – ORLADEYO: Oral, once-daily treatment for prevention of HAE attacks

    BioCryst expects three regulatory approvals for ORLADEYO in Q4 2020 and early 2021.
    The U.S. Food and Drug Administration (FDA) is reviewing a new drug application for ORLADEYO and has set an action date of 3 December 2020, under the Prescription Drug User Fee Act (PDUFA).
    In Japan, ORLADEYO is being reviewed under Sakigake designation. The Pharmaceutical and Medical Devices Agency (PMDA) has confirmed their regulatory review schedule and the company expects an approval decision in December 2020.
    On 30 March 2020, the company announced that the European Medicines Agency (EMA) had validated its marketing authorization application (MAA) submission for ORLADEYO and begun its formal review of the MAA under the centralized procedure. The company expects an opinion from the Committee for Medicinal Products for Human Use (CHMP) within approximately 12 months from MAA validation.
    BioCryst has completed significant preparations to support the launch of ORLADEYO in the U.S.
    The company has attracted an accomplished U.S. rare disease sales team, which averages 20 years in pharmaceutical sales and nearly a decade of rare disease experience.
    The company is well-positioned in terms of product supply and inventory on-hand to support the launch and anticipated global demand for ORLADEYO.
    On 9 June 2020, the company announced that it had established an expanded access program with ORLADEYO for patients with HAE in the United States. Through this program, physicians may be able to request ORLADEYO for HAE patients who do not have access to the product through a clinical trial.
    On 6 June 2020, at the European Academy of Allergy and Clinical Immunology (EAACI) Digital Congress, the company presented new data highlighting the burden of therapy faced by HAE patients taking currently available injectable prophylactic medication. Patients taking oral, once daily ORLADEYO experienced sustained decreases in their attack frequency and improvements in quality of life scores over 48 weeks. ORLADEYO was also safe and generally well-tolerated over 48 weeks in both the APeX-2 and APeX-S clinical trials.
    “Our ongoing dialogue and research with HAE patients and physicians continue to reinforce their strong demand for an oral, once-daily medicine that is safe and provides the significant and sustained attack reduction we are seeing with ORLADEYO in our clinical program. Nearly half of patients in our APeX-2 and APeX-S trials have prior experience with injectable or infused therapies and most have chosen to remain on ORLADEYO,” said Charlie Gayer, chief commercial officer of BioCryst.
    (Source: BioCryst)
    Gezien de resultaten van BioCryst zie ik ze graag snel op de markt.
  6. forum rang 4 Bram de Stratenmaker 6 augustus 2020 16:40
    quote:

    Drieklezoor schreef op 6 augustus 2020 15:54:

    De penny-stock liefhebbers regeren met ijzeren vuist , een beetje lucht erin en een beetje lucht eruit .Het lijkt wel een opdracht !! eerst moet de emotionele lucht er uit , en een positief bericht en de lucht klaart weer positief op, met dit berichtje los ik niet de problemen op , maar hoopt de twijfelaars hun aandelen niet te verkopen.
    Heb ze al vanaf dat ze 0,28euro waren, doe ze pas weg op 28,-. Als je geld hebt, en geduldig wacht, komt het vanzelf goed. Hoop ik, pfff. Zal de warmte wel zijn....
  7. [verwijderd] 6 augustus 2020 16:52
    Paar weken terug iets gepost over Postnl. Verguisd.
    Daarna iets over Plug Power.
    Zoek het maar terug.
    En ja, ik ben geen voorstander van Sijmens megalomane plannetjes. Een CEO die niet in zijn eigen unieke platform gelooft, mag van mij vertrekken.
    Met zijn 30 miljoen salesteam in de US die nog geen deuk in een pakkie boter kunnen maken.
  8. [verwijderd] 6 augustus 2020 16:59
    zo wat een hitte !
    Nu maar een Ijs en ijs eiskoude ;-)
    Tja voor hen die het vanochtend niet begreep de "Boer" is de 8.000.000 Miljoen Joker deze gooit de aandelen van rechter naar linkerhand.
    Niet te veel verschil maar een vleugje dit om te voorkomen dat mocht er nieuws komen de aandeeltjes weg zijn.

    Kom op 4.000.000 stukje waargaat dat over niks toch.

    En voor wat de expert betreft gewoon even na 17:35 de PC uit was een verlichting wederom vandaag .
    Al die onzin niet te hoeven zien wat feitelijk is het meelijden wekend je zal in deze pracht dagen aan de PC vast zitten.

    Ruud..
  9. [verwijderd] 6 augustus 2020 17:01
    quote:

    Madebeliefje schreef op 6 augustus 2020 16:52:

    Paar weken terug iets gepost over Postnl. Verguisd.
    Daarna iets over Plug Power.
    Zoek het maar terug.
    En ja, ik ben geen voorstander van Sijmens megalomane plannetjes. Een CEO die niet in zijn eigen unieke platform gelooft, mag van mij vertrekken.
    Met zijn 30 miljoen salesteam in de US die nog geen deuk in een pakkie boter kunnen maken.

    Wat dan ook niet mee valt gezien deze in de diepvries sector werkzaam zijn Madebeliefje.

    Ruud..
10.441 Posts
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