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Aandeel Pharming Group AEX:PHARM.NL, NL0010391025

Laatste koers (eur) Verschil Volume
0,765   0,000   (0,00%) Dagrange 0,765 - 0,792 2.980.262   Gem. (3M) 4,3M

donderdag 21-10-10 dag van de waarheid

281 Posts
Pagina: 1 2 3 4 5 6 ... 15 »» | Laatste | Omlaag ↓
  1. [verwijderd] 20 oktober 2010 22:26
    Ik denk dat de koers pas gaat stijgen wanneer de EPAR goedkeuring er is. Al het nieuws van morgen kan tijdelijk wat opluchting of teleurstelling geven, maar zal niet tot echte verandering in de koers (zoals 0.50) leiden. Immers, zolang die goedkeuring er niet is kunnen ze niets verkopen en blijft de toekomst onzeker.
  2. [verwijderd] 20 oktober 2010 22:51
    quote:

    jansma333 schreef:

    hoop dat we geen spijt krijgen van de keus om te blijven zitten.
    maar waar zou het morgen eindigen als het nieuws positief is? is het dan raar om te denken aan 0,50?
    heb er best veel in zitten dus hoop maar dat ik nu is keer wat terug ga pakken.
    hoelaat krijgen we iets te horen?
    Ik denk inderdaad, dat het raar denken aan de 0,50 zelfs inclusief een goedkeuring.

    Laten we eerst maar eens zien te plussen
  3. [verwijderd] 20 oktober 2010 23:07
    quote:

    Jeffreybr schreef:

    [quote=JanK1]
    [...]

    Ik denk inderdaad, dat het raar denken aan de 0,50 zelfs inclusief een goedkeuring.

    Laten we eerst maar eens zien te plussen
    [/quote]
    Wat is volgens jou realistisch dan?
    Bij positieve cijfers morgen?
    En wat bij goedkeuring?
    Ook de cijfers zullen hoogstwaarschijnlijk niet bijzonder zijn (tegenvallen), omdat de meeste betalingen pas in Q4 verwerkt worden.

    Domper zou zijn als ondanks alles alsnog gebruik zou worden gemaakt van de extra aandelen uitgifte. Helemaal als dat tegen een minimale koers zou mogen.

    Neemt niet weg dat er dan in Q4 vele positieve dingen kunnen gebeuren.
  4. pardon 21 oktober 2010 07:10
    print · email · close or Esc Key

    Pharming Announces Nine Month Financial Report 2010

    Leiden, The Netherlands, October 21, 2010. Biotech company Pharming Group NV (“Pharming” or “the Company”) (NYSE Euronext: PHARM) today published its financial report for the nine month period ended September 30, 2010.

    FINANCIAL HIGHLIGHTS FIRST NINE MONTHS
    Income from grants and license fees for the nine month period of €0.7 million (9M 2009: €0.5 million)
    Received US$15.0 million (€11.7 million) non refundable and non off-settable upfront payment from Santarus for the commercialization of Rhucin® in North America
    Received € 3.0 million upfront payment from SOBI for commercialization of Ruconest in the EU
    Significant decrease in operating cash outflows (€3.4 million in first nine months of this year compared to €18.4 million in the same period 2009)
    Operating loss of €18.3 million (9M 2009: €21.0 million)
    Cash at September 30, 2010 of €17.0 million)
    Bondholders converted all of the €7.5 million bonds issued in January 2010

    OPERATIONAL HIGHLIGHTS IN THIRD QUARTER
    Agreement entered with Santarus for the commercialization of Rhucin in North America)
    Signed manufacturing agreement with Sanofi Chimie for the drug substance of Ruconest™
    Dr Karl Keegan joined the Company as Chief Financial Officer (CFO)
    Intention to submit BLA to the FDA to obtain US marketing approval for Rhucin announced
    Spin off of DNage successfully completed

    SUBSEQUENT TO SEPTEMBER 30, 2010
    Shareholders approved appointment Dr Keegan as CFO and member of Pharming’s Management Board
    Shareholders also approved increase of the authorized share capital at Company’s EGM
    Published peer reviewed randomized clinical trial results with recombinant human C1 esterase inhibitor in Journal of Allergy and Clinical Immunology
    Anticipated exercise of the put option by the 2007 public bondholders to repay the remaining outstanding 2007 convertible bonds per 31 October 2010 was confirmed

    Sijmen de Vries, CEO, commented: “The first nine months of 2010 have been an important period for Pharming, during which we have consistently delivered on our stated targets of progressing our lead asset through the requisite developmental and regulatory pathways and maintaining tight control of our cost base. We believe that the progress we have made during the period is an endorsement of management’s strategic focus. We look forward to working with our marketing partners towards the first commercial launch of our lead program, an historic point in Pharming’s history and an important step towards bringing the Company to financial stability.”

    FINANCIAL HIGHLIGHTS FIRST NINE MONTHS
    Pharming’s income from grants and license fees were €0.7 million for the nine month period ended September 30, 2010. In the same period of 2009, Pharming recognized €0.5 million.

    Operating loss decreased to €18.3 million from the €21.0 million recorded for the corresponding period in 2009. The decrease is mainly a result of timing of (pre)clinical and regulatory activities, our continued strong focus on cost savings and control, as well as the implementation of a strategic focus of our business resulting in the spin out of DNage. In the nine month period, operating losses attributable to DNage were approximately €2.0 million compared to €2.8 million in the first three quarters of 2009. General and administrative costs remained broadly constant but R&D expenses declined by €4.5 million in the nine month period 2010 compared to the corresponding period in 2009.

    In the nine month period to September 30, 2010, Pharming recorded a net loss of €34.6 million compared to a net loss of €23.1 million for the same period in 2009. The vast majority of this loss was attributable to financing measures and their consequences that were triggered by financing activities during 2010. The net loss per share was €0.15 for the first nine months of 2010 compared to €0.22 in the first nine months of 2009. At the end of the period, the number of shares outstanding was 358,800,199 compared to 120,850,520 at the end of the corresponding period in 2009.

    The increase in the current number shares by 3,018,702 from 355,781,497 on September 2, 2010 results from 2,171,117 shares in relation to exercise of cashless warrants and 847,585 shares issued to the Board of Management and various employees in settlement of bonuses due.

    Pharming ended the nine month period with a cash position of €17.0 million, compared to a €10.6 million cash balance on September 30, 2009 and €2.3 million on December 31, 2009.

    Pharming has recorded a significant decrease in operating cash outflows (€3.4 million in first nine months of this year compared to €18.4 million in the same period 2009). This achievement is primarily related to the receipt of upfront cash payments from SOBI and Santarus. The US$15.0 million (€11.7 million) non refundable and non off-settable upfront payment from Santarus is detailed in the consolidated statement of cash flows for the third quarter. The €3.0 million upfront from SOBI was recognized similarly in Q2 2010. In accordance with International Financial Reporting Standards, Pharming will recognize these upfront payments in the consolidated statement of income from Q4 2010 onwards as the amount received spread evenly over a period of approximately 10 years.

    OPERATIONAL HIGHLIGHTS IN THIRD QUARTER
    Pharming entered into an agreement with specialty biopharmaceutical company Santarus, Inc for the commercialization of Rhucin in North America (the United States, Canada and Mexico) for the treatment of acute attacks in HAE patients and other future indications.

    Pharming signed a manufacturing agreement with Sanofi Chimie, wholly owned subsidiary of sanofi-aventis to increase the production capacity of the drug substance of Ruconest. This will improve Ruconest cost of goods and competitiveness and will put Pharming in the position to satisfy future global demand.

    Pharming announced that it intends to submit the Biologic License Application to the FDA to obtain marketing approval for Rhucin for the treatment of acute angioedema attacks in patients with HAE. Following pre-BLA discussions with the FDA, Pharming is preparing the BLA dossier for submission towards the end of this year but no later than January 2011.

    The spin off of DNage was completed and all earn-out liabilities due by Pharming to former DNage shareholders were fully settled.

    SUBSEQUENT TO SEPTEMBER 30, 2010
    Dr Karl Keegan was appointed to the role of CFO and member of Pharming’s Board of Management. Also, the increase of the authorized share capital from 400 million to 500 million shares was confirmed. These decisions were taken by the Shareholders at an Extraordinary General Meeting held on 1 October 2010.

    The publication of the integrated analysis of Pharming’s randomized placebo-controlled clinical trials with recombinant human C1 esterase inhibitor for treatment of acute angioedema attacks in HAE patients in the October issue of the peer-reviewed Journal of Allergy and Clinical Immunology.

    The anticipated exercise of the put option by the 2007 public bondholders to repay the remaining outstanding 2007 convertible bonds per October, 31, 2010 was confirmed.

    OUTLOOK Q4 2010 AND BEYOND
    Ruconest in Europe
    Following the positive opinion on the Marketing Authorization Application for Ruconest earlier this year, Pharming is antic
  5. pardon 21 oktober 2010 07:15

    LIST OF USED ABBREVIATIONS AND TERMS
    BLA Biologic License Application
    DNage DNage BV (Pharming has 51% stake)
    EGM Extraordinary General Meeting of Shareholders held on 1 October 2010
    FDA US Food and Drug Administration
    HAE Hereditary Angioedema
    rhC1INH Pharming’s recombinant human C1 esterase inhibitor
    Rhucin® Registered name in non-European countries for recombinant human C1 esterase inhibitor or rhC1INH for treatment of acute attacks of HAE
    Ruconest™ Trademark for European marketing of recombinant human C1 inhibitor for treatment of acute attacks of HAE
    Sanofi Chimie Wholly owned subsidiary of sanofi-aventis (NYSE Euronext: SAN, NYSE: SNY)
    Santarus Specialty biopharmaceutical company Santarus, Inc (NASDAQ: SNTS)
    SOBI Specialty pharmaceutical company Swedish Orphan Biovitrum (STO: BVT)

    About Pharming Group NV
    Pharming Group NV is developing innovative products for the treatment of genetic disorders, specialty products for surgical indications, and nutritional products. On June 24, the European Medicines Agency adopted a positive opinion for Ruconest™ (Rhucin® in non-EU territories) for the treatment of angioedema attacks. Market Authorization in the European Economic Area is therefore expected imminently with an anticipated market launch in the fourth quarter 2010. The product is also under development for follow-on indications, i.e. antibody-mediated rejection (AMR) and delayed graft function (DGF) following kidney transplantation. The advanced technologies of the Company include innovative platforms for the production of protein therapeutics, technology and processes for the purification and formulation of these products. Additional information is available on the Pharming website, www.pharming.com.

    This press release contains forward looking statements that involve known and unknown risks, uncertainties and other factors, which may cause the actual results, performance or achievements of the Company to be materially different from the results, performance or achievements expressed or implied by these forward looking statements.

    Contact:
    Marjolein van Helmond, T: +31 (0)71 52 47 431 or +31 (0)6 109 299 54 or E: m.helmond@pharming.com
  6. [verwijderd] 21 oktober 2010 07:31
    Door Ben Zwirs
    Van DOW JONES NIEUWSDIENST
    AMSTERDAM (Dow Jones)--Pharming Group nv (PHARM.AE) heeft een bijna 50% hoger netto verlies geleden over de eerste negen maanden van 2010 vanwege oplopende financieringslasten, maar realiseerde wel voor de eerste keer aanzienlijke inkomsten.
    Het bedrijf uit Leiden kreeg $15 miljoen binnen van Santarus voor een commerciele deal voor Rhucin in de VS en EUR3 miljoen van SOBI voor Ruconest, de merknaam van Rhucin in de Europese Unie.
    Het nettoverlies over de eerste drie kwartalen van dit jaar bedraagt EUR34,6 miljoen, tegen EUR23,1 miljoen over dezelfde periode van 2009. Pharming schrijft deze toename toe aan financieringsmaatregelen die in 2010 werden genomen.
    Pharming ontving in juni een positieve opinie van de Europese medicijnentoezichthouder EMA voor het middel tegen acute aanvallen van erfelijke angio-oedeem en verwacht binnen enkele weken definitieve toestemming van de Europese Commissie om het medicijn op de Europese markt te brengen. Dit zal gepaard gaan met een mijlpaalbetaling van SOBI.
    Verder wil Pharming het medicijn in de Verenigde Staten op de markt brengen. Het concern verwacht hiertoe eind dit jaar en niet later dan januari 2011 een aanvraag te doen bij de Amerikaanse toezichthouder.
    De kaspositie aan het eind van het derde kwartaal bedroeg EUR17,0 miljoen, in vergelijking met EUR2,3 miljoen eind 2009.
    Door Ben Zwirs, Dow Jones Nieuwsdienst: +31-20-5715210; ben.zwirs@dowjones.com
    (END) Dow Jones Newswires
    October 21, 2010 01:26 ET (05:26 GMT)
    © 2010 Dow Jones & Company, Inc.

    AAND PHARMING GROUP @ EUR 0.04
    NL0000377018
  7. [verwijderd] 21 oktober 2010 07:39
    Gepubliceerd: vandaag 07:36

    LEIDEN (AFN) - Biotechnologiebedrijf Pharming verwacht dat de Europese Commissie binnen enkele weken definitief het licht op groen zal zetten voor toelating van zijn geneesmiddel Ruconest op de Europese markt. Dit liet het bedrijf donderdag weten bij de publicatie van de derdekwartaalresultaten.

    Pharming zal zich in de rest van het jaar concentreren op de Europese lancering van Ruconest, een behandeling voor zwellingen van zachte weefsels. Tegelijk met de goedkeuring krijgt Pharming een tweede mijlpaalbetaling van zijn Europese partner Swedish Orphan Biovitrum (SOBI).

    In het afgelopen kwartaal draaide het bedrijf een operationeel verlies van 6,6 miljoen euro, ongeveer evenveel als in dezelfde periode in 2009. De onderneming had eind september bijna 17 miljoen euro in kas.



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281 Posts
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