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Aandeel Pharming Group AEX:PHARM.NL, NL0010391025

Laatste koers (eur) Verschil Volume
0,805   +0,028   (+3,54%) Dagrange 0,780 - 0,808 3.256.008   Gem. (3M) 3,9M

Pharming oktober 2018

12.923 Posts
Pagina: «« 1 ... 287 288 289 290 291 ... 647 »» | Laatste | Omlaag ↓
  1. [verwijderd] 17 oktober 2018 07:43
    quote:

    BioTics schreef op 17 oktober 2018 07:36:

    Maar ja hoe goed is dit goede bericht, dat is mijn grote vraag.
    Leuke reactie HOOR!verdiep je er in en kom dan nog eens terug.

    Beleggers, gefeliciteerd en al zal de koers niet meteen bokkensprongen maken, de kansen om uit te groeien nemen toe.

    Succes en meneer De Vries,

    Bedankt,

    Mini
  2. marcko 17 oktober 2018 07:44
    Het zijn 2 goede berichten. Eerste is goede Basel resultaten Mbt nefropathie (nierbeschadiging)
    2e is; Zoals gepland heeft Pharming goedkeuring aangevraagd in Nederland en binnenkort in Australië om te mogen starten met de eerste klinische studie van RUCONEST® in pre-eclampsie (zwangerschapsvergiftiging).
  3. jakhals 17 oktober 2018 07:46
    Pharming Reports Positive Data From First Investigator-initiated Study of rhC1-Inhibitor (RUCONEST®) in Contrast-induced Nephropathy

    NEWS PROVIDED BY

    Pharming Group N.V. 

    06:00 BST

    LEIDEN, Netherlands, October 17, 2018/PRNewswire/ --

    Primary Endpoint was met, with rhC1INH treatment reducing neutrophil gelatinase-associated lipocalin (NGAL), a widely recognized marker of acute renal damage 

    Pharming Group N.V. ("Pharming" or "the Company") (Euronext Amsterdam: PHARM) today announced positive results from a Phase II investigator-initiated study of RUCONEST® (recombinant human C1 esterase inhibitor, or "rhC1INH") in a double-blind, placebo-controlled clinical trial in patients at risk of nephropathy resulting from contrast-enhanced examinations.

    The study was led by Dr. Michael Osthoffat the University Hospital Basel, Basel, Switzerland.  75 eligible patients with known moderate to severe renal function impairment were given either 50 units per kg (up to 4200 units) of RUCONEST® (n=37) or placebo (n=38) immediately prior to treatment with standard-of care contrast medium as part of an elective coronary angiography with or without a percutaneous coronary intervention ("PCI"), and then a second identical treatment four hours after the intervention .

    In the overall study, RUCONEST® showed a statistically-significant effect (p= 0.038) in reducing the rise in urinary Neutrophil Gelatinase-Associated Lipocalin (NGAL), the primary endpoint for the study and a generally recognized early marker of acute renal injury, in patients with diagnosed renal function impairment undergoing interventions enhanced with standard contrast media such as PCIs.

    The results were especially clear in the sub-group of patients (n=30) undergoing PCI. The intent-to-treat analysis in this group showed that patients on RUCONEST® had a median increase in peak urinary NGAL concentration within 48 hours of 1.8 ng/ml compared with an increase of 26.2 ng/ml in the placebo arm (p=0.04). This corresponds to a clear difference in the median percentage change in the peak urinary NGAL level within 48 hours of 11.3% in the RUCONEST® arm and 205.2% in the placebo arm (p=0.001).

    The overall assessment of the study also showed trends that patients undergoing more invasive interventions and procedures requiring higher volumes of contrast medium experienced a stronger benefit from the RUCONEST® treatment.

    The treatment also showed an excellent safety profile comparable to the placebo group - a particularly significant observation considering the high-risk patient group included in the study (average age approximately 77 years, with multiple comorbidities and impaired kidney function)

    This data therefore supports additional clinical investigations for the use of rhC1INH in a new indication where there is significant unmet medical need.

    A secondary endpoint measured was Troponin T, a marker of cardiovascular damage caused by the examination or intervention itself, but this did not show a meaningful difference in the overall study population: the power of the study and the variety of interventions applied were 
    www.prnewswire.co.uk/news-releases/ph...

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