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INSM - Insmed - 2009 draadje

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  1. ludwig mack 4 maart 2011 10:38
    voor ongeduld had je al lang weg moeten zijn, maar goed, dat is altijd zo;
    ik wacht en zeker als het jaren duurt, zal het wat opbrengen want octrooi komt gewoon los, en dan nog los van andere toepassingen en wat de nw dochter gaat doen, en dan heb ik het nog niet eens over de cash die ze hebben, want dat maakt geduld hier mogelijk, in ieder ander geval niet ..........

    gr
  2. [verwijderd] 5 maart 2011 04:03
    [quote=ludwig mack]
    voor ongeduld had je al lang weg moeten zijn, maar goed, dat is altijd zo;
    ik wacht en zeker als het jaren duurt, zal het wat opbrengen want octrooi komt gewoon los, en dan nog los van andere toepassingen en wat de nw dochter gaat doen, en dan heb ik het nog niet eens over de cash die ze hebben, want dat maakt geduld hier mogelijk, in ieder ander geval niet ..........

    gr
    [/quote
    Al lang weg? Ik zit er al jaren in hoor Ludwig. Nu reken ik op wat institutionelen die de boel gaan pompen. Eerlijkheid gebied me te zeggen dat vorig management in de tijd dik gefaald heeft. De rechtzaak heeft er maar 1 rijk gemaakt, en die ligt nu rustig. Hier kan je toch niet spreken over ongeduld?? Koop dan Anik of zo, om het even. Die overname zit me gewoon totaal dwars.
    Dit is Insmed niet.
  3. [verwijderd] 5 maart 2011 13:08
    Ik ben het met je eens Jef. Maar Premacure is nog steeds bezig met premies en premiplex, en misschien krijgen we nog nieuws van pcut en een ALS trial ..
  4. [verwijderd] 5 maart 2011 16:09
    Pulmonary NTM is estimated by some experts in the field to be at least ten times more common than TB in the U.S., with at least 150,000 cases per year.
    en.wikipedia.org/wiki/Nontuberculous_...

    If the rate is similar in Europe, as the Pseudomonas indication was, that's a total US/EU patient population of 300K in this indication.

    Priced at 15,567 per annum, that's a market of very roughly $4,670,100,000 (all the caveats on the per annum cost from my previous post).

    The PR states: "The drug's previously completed Phase 2 and earlier stage clinical studies highlighted the potential of ARIKACE™ to become a leading treatment in two high-growth orphan indications with significant unmet medical needs

    Als dit de marktwaarde word in de toekomst dan is een koers van 186,00 dol. niet eens zo gek met het huidige aantal uitstaande aandelen!

    Yok
  5. ludwig mack 7 maart 2011 11:30
    quote:

    jefke101 schreef op 5 maart 2011 04:03:

    [quote=ludwig mack]
    voor ongeduld had je al lang weg moeten zijn, maar goed, dat is altijd zo;
    ik wacht en zeker als het jaren duurt, zal het wat opbrengen want octrooi komt gewoon los, en dan nog los van andere toepassingen en wat de nw dochter gaat doen, en dan heb ik het nog niet eens over de cash die ze hebben, want dat maakt geduld hier mogelijk, in ieder ander geval niet ..........

    gr
    [/quote
    Al lang weg? Ik zit er al jaren in hoor Ludwig. Nu reken ik op wat institutionelen die de boel gaan pompen. Eerlijkheid gebied me te zeggen dat vorig management in de tijd dik gefaald heeft. De rechtzaak heeft er maar 1 rijk gemaakt, en die ligt nu rustig. Hier kan je toch niet spreken over ongeduld?? Koop dan Anik of zo, om het even. Die overname zit me gewoon totaal dwars.
    Dit is Insmed niet.
    die financ. expert voor een overname kijkt naar kansen en niet perse naar zelfde segment van de oer insm, anders hadden ze fabriek bijvoorbeeld ook niet hoeven te verkopen ......

    aangezien cash king is in deze tijden, verwacht ik nog meer, en weer leuke post van yok ;-)
  6. [verwijderd] 10 maart 2011 14:15

    Insmed Announces Fourth Quarter and Full-Year 2010 Financial Results
    RICHMOND, Va., March 10, 2011 /PRNewswire/ -- Insmed Inc. (Nasdaq CM: INSMD), a biopharmaceutical company, today reported results for the fourth quarter and full-year ended December 31, 2010.
    Key Recent Highlights:
    • Filed Investigational New Drug (IND) Application in February 2011 with the FDA to begin a phase 3 clinical trial for ARIKACE™ (liposomal amikacin for inhalation) in non-TB Mycobacteria (NTM) lung infections.
    • Successfully concluded 72 week phase 2b open-label study for ARIKACE for pseudomonas lung infections in cystic fibrosis (CF) patients.
    • Received positive opinion from European Medicines Agency (EMA) on Company's Pediatric Investigation Plan for ARIKACE in the CF indication.
    • Gained shareholder approval for conversion of preferred stock into common stock and 1:10 reverse stock split.

    "Following the closure of our transformative business combination in December 2010, we have been aggressively moving forward with the development plan for ARIKACE, our phase 3 compound for pseudomonas lung infections for CF patients, and NTM lung infections," said Timothy Whitten, Insmed's President & CEO. "We are well underway with the initial preparations and necessary work around these trials and continue to expect to begin accruing patients to the phase 3 trials in both indications in the second half of 2011, with results expected in the first half of 2013."
    Financial Results
    On March 1, 2011, at a special meeting, our shareholders approved a one for 10 reverse stock split of our common stock, which became effective at 5:00 pm EST on March 2, 2011. This reverse stock split is reflected in the shares outstanding and earnings per share calculations below.
    Revenues for the fourth quarter ended December 31, 2010 were $1.3 million, as compared to $2.5 million for the corresponding period in 2009. The $1.2 million decrease resulted from $0.6 million in lower cost recovery from our IPLEX™ Expanded Access Program (EAP) in Europe, $0.5 million of IPLEX grant revenue which was recognized in the fourth quarter of 2009 and $0.1 million in lower royalties during the most recent period. The reduction in the IPLEX cost recovery was due to the Company's decision in July 2009 to cease supplying the drug to new patients in order to preserve the remaining IPLEX inventory for patients currently receiving the drug. The $0.5 million reduction in grant revenue related to a grant received in the fourth quarter of 2009 from the Muscular Dystrophy Association (MDA) for the previously completed IPLEX Phase 2 Myotonic Muscular Dystrophy trial. The reduced royalty was due to the expiration of a TGF- beta royalty in 2010.
    In the fourth quarter of 2010, the Company posted a net loss of $5.8 million, or $0.42 per share, as compared to a net profit of $2.3 million, or $0.18 per share, in the fourth quarter of 2009. The $8.1 million variance arose from a $5.5 million increase in total expenses, the elimination of a $2.0 million tax refund which occurred in 2009 and a $1.2 million reduction in revenue. These were partially offset by a $0.6 million improvement in investment income.
    The $5.5 million increase in total expenses resulted from a $1.7 million increase in research and development expenses (R&D Expenses) and a $3.8 million increase in selling, general and administrative expenses (SG&A Expenses). The higher R&D Expenses were due primarily to the addition of ARIKACE-related R&D Expenses in December 2010, while the increase in SG&A Expenses resulted from increased external finance, legal and consulting expenses related to the business combination, and the addition of ARIKACE-related support costs for December 2010.
    The $2.0 million tax impact resulted from the utilization of Net Operating Losses in the fourth quarter of 2009, which reduced the amount of taxes paid on the gain on sale of Insmed's follow-on biologics (FOB) assets to Merck in March 2009. The lower interest expense was due to the reduction of the debt discount amortization associated with the Company's 2005 convertible notes which were fully paid off in 2010.
    For the year-ended December 31, 2010, revenues totalled $6.9 million, as compared to $10.4 million for the year-ended December 31, 2009. The reduction was primarily due to a year-over-year decrease of $2.3 million in cost recovery from Insmed's IPLEX EAP in Europe, a $1.0 million reduction in grant revenue related to the 2009 receipt of a $1.0 million grant from the MDA and $0.1 million in reduced royalties. The causes of the fourth quarter revenue variance were also responsible for the full-year differences in revenue between 2010 and 2009.
    Net loss for the 12-months ended December 31, 2010 was $6.4 million, or $0.49 per share, compared to a net income of $118.4 million, or $9.31 per share, for the corresponding 12-months of 2009. This $124.8 million variance was due to the $127.0 million after tax gain on the sale of the Company's FOB assets to Merck in 2009, combined with a $3.5 million decrease in total revenues. These were partially offset by a $4.0 million reduction in total expenses, a $1.0 million increase in investment returns and a $0.7 million decrease in interest expense.
    The $4.0 million decrease in total expenses was due to a $4.4 million reduction in R&D Expenses, which was partially offset by a $0.4 million increase in SG&A Expenses. The $4.4 million reduction in R&D Expenses was due primarily to a decrease in manufacturing expenses following the sale of Insmed's FOB assets in March 2009, and was partially offset by the ARIKACE-related R&D Expenses incurred in December 2010. The $0.4 million increase in SG&A Expenses was due largely to the increased finance, legal and consulting fees related to the strategic review and the business combination with Transave on December 1, 2010. The improved return on investments reflected the increased cash position and higher yield rates, while the lower interest expense was due to the elimination of the debt discount amortization.
    As of December 31, 2010, Insmed had total cash, cash equivalents, short-term investments, and certificate of deposits on hand of $110.2 million, consisting of $108.0 million in cash and short-term investments and $2.2 million in a certificate of deposit, as compared to $124.3 million of cash on hand as of December 31, 2009. The $14.1 million decrease in total cash was due to the $8.0 million full payment of Transave debt at the time of the merger, together with the payment of approximately $6.1 million in costs primarily related to the strategic review during 2010 and the business combination with Transave.
  7. ludwig mack 13 maart 2011 15:33
    van de laatste c.call haal ik dit van message board, om in de gaten te houden op een lijstje / of in je hoofd ;-):

    Msg 28518 of 28536 at 3/10/2011 8:45:31 AM by

    WisemanFromEast





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    Any iplex initative will be announced before 2011 end
    Arikase is the primary product going forward and any decision or initative regarding Iplex will be announced before end of 2011.

    He said 32 ALS patients on Iplex (26 Europe and 6 in US). Inventory is available upto Aug end of 2011.

    I think they said 5 ROP patients on Iplex?

    So what I've heard was ==> INSM as a company is banking on Arikace! Major conference in Europe coming in June (so that sounds like the next milestone).

  8. [verwijderd] 16 maart 2011 20:27
    De marketmakers/shorters zien hun kans weer schoon om de boel lekker naar beneden te drukken zolang er geen nieuws is, hopelijk komt er wel wat de komende tijd!!!

    Yok
  9. gustaaf1e 16 maart 2011 21:22
    ah mensen,
    meevallertje.
    Op de valreep boven de $5,- gezet.
    Lijkt me een afspraak om 'm boven de 5 te houden.
    En dat is in deze dramatische dagen niet sjlecht.
    Voor hogere koers is goed nieuws nodig. Komt wel.
    G
  10. [verwijderd] 16 maart 2011 21:45
    xml.10kwizard.com/filing_raw.php?repo...

    TriAct

    On December 20, 2010, we entered into an agreement with TriAct Therapeutics Inc, whereby TriAct obtained an exclusive license from Insmed for INS-18 also known as Masoprocal. The license gives TriAct the right to develop, manufacture and commercialize Masoprocal products for any indications relating specifically to Oncology. The agreement calls for the issue of TriAct common stock to Insmed upon the achievement of certain milestones. To date, no common stock has been received.

    Eleison

    On February 1, 2011, we entered into an agreement with Eleison Pharmaceuticals whereby Eleison obtained an exclusive license from Insmed for Inhaled Cisplatin Lipid Complex. The license gives Eleison the right to develop, manufacture and commercialize inhaled Cisplatin Lipid Complex for cancers affecting the lung. The agreement calls for payments from Eleison to us upon the achievement of certain milestones.

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