Insmed Incorporated Message Board

migraine_jane 3 posts  |  Last Activity: Apr 28, 2013 1:25 PM Member since: Jan 6, 2000
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  • Reply to

    April 30th WL Presents . . .

    by rehdvm2004 Apr 27, 2013 5:30 PM
    migraine_jane migraine_jane Apr 28, 2013 1:25 PM Flag

    I realize it's early in the game and news will be coming in fits and starts but I would be curious what everyone thinks would be a satisfactory price if a buyout were to occur.

    I like historian's $18 (pre r/s) price but I don't know how long I would be willing to wait for it.

  • migraine_jane by migraine_jane Mar 28, 2013 9:25 AM Flag

    "50,000 cases of NTM lung disease were treated by physicians in the U.S. during 2011. There is no current FDA-approved treatment for NTM lung infection."

  • migraine_jane migraine_jane Mar 12, 2013 3:51 PM Flag

    (Reuters) - Shire increased its investment in rare diseases on Tuesday by acquiring privately held Swedish biotech firm Premacure, which is developing a drug for a potentially blinding eye disorder in premature babies.

    Britain's third biggest drugmaker did not reveal how much it was paying for the Uppsala-based business but said it would pay a sum upfront followed by contingent payments based on clinical development and commercial success.

    The acquisition takes Shire into the new area of neonatology - the treatment of sick or premature newborn infants - and expands its already substantial presence in rare diseases.

    Treating diseases that affect only a small number of patients is a growing focus for many drug companies given the high prices that can be achieved.

    Premacure, which was launched in 2006, has an experimental protein replacement medicine in mid-stage Phase II clinical development for the prevention of retinopathy of prematurity (ROP).

    Normal full-term babies produce enough growth factors on their own to prevent diseases like ROP. But those born before 31 weeks may lack chemicals such as insulin-like growth factor 1 (IGF-1), which can result in life-long complications like ROP.

    Shire said its human genetic therapies unit would continue with the Phase II study, the primary goal of which is to restore the IGF-1 levels in premature infants to those found in babies born at full term.

INSM
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