Ontvang nu dagelijks onze kooptips!

word abonnee
Van beleggers
voor beleggers
desktop iconMarkt Monitor
  • Word abonnee
  • Inloggen

    • Geen account? Registreren

    Wachtwoord vergeten?

Aandeel Pharming Group AEX:PHARM.NL, NL0010391025

Laatste koers (eur) Verschil Volume
0,695   +0,005   (+0,72%) Dagrange 0,688 - 0,705 2.315.672   Gem. (3M) 3,2M

Friday 19-08-2011

22 Posts
Pagina: 1 2 »» | Laatste | Omlaag ↓
  1. superb04 19 augustus 2011 12:19
    Alles verkocht na jaren lang in Ph te hebben gezeten. Dik verlies, maar het zeit zo. Rest bedrag maar in Ageas gestoken. Pijn in het hart, maar Ph doet gewoon helemaal niets inclusief die blaaskaak van Ph die dingen beloofd (25 ct) en andere onzin roept.

    Succes en misschien tot betere tijden:)
  2. machmit 19 augustus 2011 14:05
    Angst is zoals bekend een slechte raadgever. Maar hoe ontkom je daaraan als je als kleine belegger dagen achtereen bestookt wordt met negatieve beursberichten. Niet dat het de bedrijven zo slecht gaat, maar de politici laten het afweten, in de VS, in Europa. Voeg daarbij berichten over het recente ongeluk in België, de hongersnood in de Hoorn van Afrika, de rellen in Groot-Brittannië, de slachtpartij in Noorwegen, om maar te zwijgen van de gebeurtenissen in Syrië en Lybië. Somber kun je ervan worden, maar die somberheid, die mineurstemming moet er niet toe leiden om geprikkeld te raken en als gevolg daarvan op dit forum elkaar eens flink de maat te nemen. Kop op, er komen weer betere tijden, zeker voor Pharming.
  3. [verwijderd] 19 augustus 2011 15:36
    Tja,ik weet natuurlijk niet of nu nog durf heb om zomaar een linkje neer te plempen,maarja beter iets dan niets,ga ik het toch wagen.

    Heeft het met Pharming van doen,ach,dat ligt aan uw eigen fantasie cq inlevingsvermogen.

    seekingalpha.com/article/288315-salva...

    Vriendelijke groet.
  4. juliozunderglas 19 augustus 2011 16:34
    ll-clear to start treating patients in the U.S. Phase IIIb study of Rhucin in the treatment of acute attacks of angioedema after reaching agreement with the FDA to expand the trial and modify the way the primary endpoint is assessed.

    The approval, under a special protocol assessment, brings Pharming (PHUGF.PK) closer to triggering $15 million in milestone payments from its North American marketing partner Santarus Inc., of San Diego, with $10 million due on reaching the primary endpoint in the study and $5 million on filing the biologics license application.

    "It's now absolutely clear what is required to complete the study," said Sijmen de Vries, CEO, in a conference call. The redesign means a 50 percent increase in the number of patients, from 50 to 75. However, de Vries said Pharming has been opening new sites and screening patients for eligibility while awaiting the FDA's go-ahead, allowing recruitment to start immediately.

    As a result the trial of Rhucin, a recombinant human C1 inhibitor manufactured from the milk of transgenic rabbits, is still expected to complete by the third quarter of 2012. That was the timing forecast when the Phase IIIb started in February, before the FDA asked for the protocol to be altered.

    "The $10 million [milestone] is within reach, but it's difficult to say exactly when. It's not a huge study, and we have got patients in the wings, waiting to be treated," de Vries said. The endpoint is time to onset of relief of symptoms.

    If approved, Rhucin will be the first recombinant C1 inhibitor on the market in the U.S. However, competition in the U.S market for treating acute attacks in patients with hereditary angioedema is ramping up, following the approval in October 2009 of CSL Behring's Berinert.

    In June an FDA advisory committee recommended approval of Shire Pharmaceuticals plc's Firazyr. The PDUFA date is Aug. 25, and Shire has said it expects to launch the product before the end of the year. If it gets the nod, Firazyr will be the first treatment for acute attacks of angioedema that can be self-administered.

    Firazyr and Rhucin already are in competition in Europe, where Rhucin (known as Ruconest) was launched in December 2010. Ruconest is now available in Scandinavia, France, UK and Germany. De Vries said there has been "a lot of feedback" from key opinion leaders to the launch and "a lot of general acceptance" that Ruconest will be used to treat acute angioedema. But it is too early to define the profile of the patients who are getting the drug, de Vries said.

    Revenues to Pharming in the second quarter from Ruconest sales were a modest ¬200,000 (US$283,000). However, that represented a 26 percent increase over the first three months of the year, and de Vries said he expects it will be 12 months before Ruconest is rolled out to all European country markets.

    Current sales are from inventory manufactured using an earlier, inefficient process, resulting in a low margin. Pharming has devised a better method for making Ruconest and is in the middle of transferring the technology over to Sanofi-Chemie, which has been contracted to manufacture the drug. This will lead to improved margins for Leiden, the Netherlands-based Pharming, though de Vries noted that the company owns the existing inventory: "From a margin perspective it doesn't look pretty, but it's all paid for, so it's all cash in."

    Cash however, remains a serious preoccupation. In the six months to June Pharming raised ¬10.2 million, and more recently a further ¬3.2 million in a private placement. But that only gives enough resource to last until the second quarter of 2012, leaving a gap before the expected end of the U.S. Phase IIIb trial triggers milestones from Santarus.

    The company has been busy trimming expenditures, most recently announcing the closure of its DNage subsidiary, cutting cash burn by ¬1.6 million in the first six months of 2011, compared to a year earlier. Karl Keegan, CFO said that, "like any biotech," Pharming is looking at lots of different ways of financing the company. Shareholders have faced a lot of dilution over the past two years, and Keegan said he is "cognizant of the fact that shareholders are wary of further dilution."
22 Posts
Pagina: 1 2 »» | Laatste |Omhoog ↑

Meedoen aan de discussie?

Word nu gratis lid of log in met je emailadres en wachtwoord.