% | $
Quotes you view appear here for quick access.

Insmed Incorporated Message Board

  • fudfighter3 fudfighter3 Mar 18, 2014 1:03 PM Flag

    TV program last night on MDR-TB


    This was a ninety minute program - TB:Return of the Plague.

    "A deadly airborne disease is making a dramatic comeback. Passed on by a cough or a sneeze, TB is travelling fast."

    They claimed around half a million people a year are currently developing MDR-TB.

    I only watched the first half and hour or so, which focussed on a young girl (aged about 8 I think) in Africa who had just been diagnosed with MDR-TB.

    Started off with a health care lady breaking the news to her that, to protect her family, she would have to spend the next two years in a TB hospital.

    At the hospital she was told that the first six months of treatment would include a daily injection in the buttocks. She was warned about the danger of side effects - the most serious of which is that some patients lose their hearing. They told her to immediately report any ringing in the ears.

    An older girl who'd been there a while had been constantly sick from the tablets, to such an extent that her treatment had to be stopped for a while to allow her to regain weight.

    The tablets used to treat routine cases of TB also cause side effects such as nausea. The program attributed the MDR-TB epidemic to breaks in therapy for routine TB because of the side effects.

    The injections (though it wasn't mentioned) had to have been an aminoglycoside such as amikacin.

    But here WE are - possibly a matter of days away from clinical trial results proving that Arikace can deliver an effective concentration of aminoglycoside to a pulmonary mycobacterial infection (such as MDR-TB) without the risk of hearing loss.

    And we have an analyst suggesting that proof of efficacy may not be sufficient to warrant approval unless some of the patients were CURED by six months of therapy - when the minimum recommended period of therapy for a drug-resistant pulmonary mycobacterial infection is currently two years.

    Priceless :-)

    This topic is deleted.
    SortNewest  |  Oldest  |  Most Replied Expand all replies
    • In case Arikace does indeed become available in Canada before the accelerated approval process makes it available in the US - it's worth noting that a 1991 study by the U.S. General Accounting Office found that one-third of all drug administrations to cancer patients were off-label.

      30,000 in the US with Cystic Fibrosis plus 50,000 treated for pulmonary NTM each year would generate substantial off-label use.

      The best antibiotic currently available for CF can only halt the relentless deterioration in lung function for a month or two at most. Data recently released show that Arikace halted deterioration for a year (and counting).

      As for NTM antibiotics, here's an excerpt from Dr. Ken Olivier's presentation at the 2013 European CF conference (thanks Blase) -

      [ M. avium complex may be easier to treat, using daily oral macrolide (preferably azithromycin), rifampin, and ethambutol, for clarithromycin-sensitive M. avium complex. ]

      Infections by Non-Tuberculosis Mycobacteria (such as MAC) and Mycobacterium Tuberculosis are treated with the same antibiotics - those which have evidenced efficacy in killing mycobacteria sheltering within the pulmonary macrophages (which usually digest bacteria).

      Here are the common side-effects -

      Amikacin ..... kidney and ear problems.
      Azithromycin ..... nausea, headaches, vomiting, diarrhea.
      Ciprofloxacin ..... nausea, vomiting, diarrhea.
      Clarithromycin ..... nausea, headaches, vomiting, diarrhea. Note: The maximum dose is 500 milligrams twice a day.
      Ethambutol ..... nausea, vomiting, vision problems.
      Rifabutin ..... rashes, nausea, anemia. Many drug interactions.
      Rifampin ..... fever, chills, muscle or bone pain; can turn urine, sweat, and saliva red-orange (may stain contact lenses); can interfere with birth control pills. Many drug interactions.

      Decide for yourselves the potential of Arikace if it does indeed deliver an effective concentration of amikacin without the systemic toxicity which causes those side-effects.

    • Who is that brilliant analyst for clarification purposes?

14.48-0.18(-1.23%)10:24 AMEDT