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Interesting proposal for cutting cancer drug costs which, you can see, relates .....

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    Interesting proposal for cutting cancer drug costs which, you can see, relates .....

    I know this does not help us old timers but...it is the way things should be done.

    By Ben Hirschler for Reuters
    LONDON, Feb 9 (Reuters) - A group of academic researchers has demanded an end to cancer medicines costing more than $100,000 a year and proposed a new model of low-cost drug development that would capitalise on recent advances in science.

    The spiralling cost of cancer medicines is a growing concern for doctors and their patients, many of whom struggle to pay for new medicines that often cost $10,000 a month.

    Sky-high prices have made oncology hugely profitable, with IMS Health forecasting global cancer drug sales of at least $150 billion by 2020. Scientists, however, believe today's prices are simply not sustainable as more and more people need treatment.

    Writing in the journal Cell on Thursday, European and U.S. experts laid out a blueprint for reining in costs by increasing the role of academic research groups, working alongside new kinds of private companies, in the development of new drugs.

    Rather than simply licensing discoveries to Big Pharma, academic groups should in future consider working with smaller companies that commit to capping prices, low-cost generic drug companies or non-profit organisations, they said.

    "Something has to change. This is a call to arms," Paul Workman, one of the paper's authors and chief executive of Britain's Institute of Cancer Research, told Reuters.

    "Charging $100,000 is unsustainable. We need to be thinking about getting prices down towards a half or a third of that, ideally even less."

    The call coincides with growing political pressure on the issue, including an attack on high drug prices by U.S. President Donald Trump.

    Workman, whose institute has discovered 20 drug candidates since 2005, believes cancer drug prices have become disconnected from economics as companies charge what the market will bear rather than a price reflecting costs.

    A principal justification for high prices is the financial burden of running large clinical trials to secure regulatory approval. Yet this increasingly does not apply in the case of modern cancer therapies.

    For example the registration study for Pfizer's targeted lung cancer drug Xalkori required only 347 patients, while last year's extended approval of the medicine to patients with mutations in the ROS1 gene involved only 50 subjects.

    Workman, together with colleagues from the MD Anderson Cancer Center in Texas and the Netherlands Cancer Institute, said the solution was for an increasing proportion of drug developments to be driven by academia.

    To an extent that is already happening. Many of the latest advances in cancer treatment originate in academic labs and there are now nearly 150 academic drug discovery centres around the world, 80 percent of which develop oncology products.

    Those academic centres should in future focus not only on getting their discoveries to market but also on securing drug price caps as part of their negotiations with commercial partners, the authors said.

    Increasing the scale and expertise of academic centres will take time and money, but in the long term the new competition should also help drive down prices in conventional pharma and biotech, they said.

    (Editing by Greg Mahlich)
    Linda~~~~

    Be the kind of woman that when your feet hit the floor each morning the devil says:"Oh Crap, She's up!"..

    #2
    I'm not sure how I'd feel about this proposal if I had a cancer for which there seemed to be no option other than some costly drug but I'd like to think I'd prefer just to let nature take its course instead of taking the drug. You have to wonder if the market should be supplied with so many costly drugs just because they can be produced.

    The drug companies keep rolling them out, apparently trusting that someone will find the money to pay for them.
    SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

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      #3
      Originally posted by agate View Post
      I'm not sure how I'd feel about this proposal if I had a cancer for which there seemed to be no option other than some costly drug but I'd like to think I'd prefer just to let nature take its course instead of taking the drug. You have to wonder if the market should be supplied with so many costly drugs just because they can be produced.

      The drug companies keep rolling them out, apparently trusting that someone will find the money to pay for them.
      I'm not sure what to say Agate.
      The point of this article is to return the research and development to universities..to academia. I don't know how but it was allowed to shift to the drug companies. This proposal would return the R&D to universities where profit is not the primary end point.

      Also, we do pay huge amounts for our MS drugs precisely because they are owned by the drug companies that developed them. It cost me $1,000 a month for the years I took the ABCs. It cost $70,000.00 a month for the eight years I took IVIG.
      I think the rituxan I now use is only $70,000.00 a year. Only $70,000!!!

      So, the proposal in the article gives power back to the scientists. DOesn't it? Maybe I read it incorrectly?
      Linda~~~~

      Be the kind of woman that when your feet hit the floor each morning the devil says:"Oh Crap, She's up!"..

      Comment


        #4
        Originally posted by Lazarus View Post
        I'm not sure what to say Agate.
        The point of this article is to return the research and development to universities..to academia. I don't know how but it was allowed to shift to the drug companies. This proposal would return the R&D to universities where profit is not the primary end point.

        Also, we do pay huge amounts for our MS drugs precisely because they are owned by the drug companies that developed them. It cost me $1,000 a month for the years I took the ABCs. It cost $70,000.00 a month for the eight years I took IVIG.
        I think the rituxan I now use is only $70,000.00 a year. Only $70,000!!!

        So, the proposal in the article gives power back to the scientists. DOesn't it? Maybe I read it incorrectly?
        No, that's the way I read it too, Linda. My post must not have been very clear.

        The result should be a lowering of the cost of some drugs that could turn out to be ridiculously expensive. Copaxone was costing $30,000 a year when I was taking it, and it costs much more now.

        Avonex was in a similar price range.

        If drugs that are just as good but cost less can be made with more involvement from research universities and less from Big Pharma, that would be great.
        SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

        Comment


          #5
          "The call coincides with growing political pressure on the issue, including an attack on high drug prices by U.S. President Donald Trump."

          Nothing to add.
          "Given the millions of billions of Earth-like planets, life elsewhere in the Universe without a doubt, does exist."

          Albert Einstein

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