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    4
    Jan
    2013
    10:46am, EST

    Indian court to rule on generic drug industry

    By Nirmala George, The Associated Press

    From Africa's crowded AIDS clinics to the malarial jungles of Southeast Asia, the lives of millions of ill people in the developing world are hanging in the balance ahead of a legal ruling that will determine whether India's drug companies can continue to provide cheap versions of many life-saving medicines.

    The case — involving Swiss drug maker Novartis’s cancer drug Gleevec — pits aid groups that argue India plays a vital role as the pharmacy to the poor against drug companies that insist they need strong patents to make drug development profitable. A ruling by India's Supreme Court is expected in early 2013.

    "The implications of this case reach far beyond India, and far beyond this particular cancer drug," said Leena Menghaney from the aid group Doctors Without Borders. "Across the world, there is a heavy dependence on India to supply affordable versions of expensive patented medicines."

    With no costs for developing new drugs or conducting expensive trials, India's $26 billion generics industry is able to sell medicine for as little as one-tenth the price of the companies that developed them, making India the second-largest source of medicines distributed by UNICEF in its global programs.

    Indian pharmaceutical companies such as Cipla, Cadila Laboratories and Lupin have emerged over the past decade as major sources of generic cancer, malaria, tuberculosis and AIDS drugs for poor countries that can't afford to pay Western prices.

    The 6-year-old case that just wrapped up in the Supreme Court revolves around a legal provision in India's 2005 patent law that is aimed at preventing companies from getting fresh patents for making only minor changes to existing medicines — a practice known as "evergreening."

    Novartis argued that a new version of Gleevec — marketed in Europe and India as Glivec — was a significant change from the earlier version because it was more easily absorbed by the body.

    India's Patent Controller turned down the application, saying the change was an obvious development, and the new medicine was not sufficiently distinct from the earlier version to warrant a patent extension.

    Patient advocacy groups hailed the decision as a blow to "evergreening."

    But Western companies argued that India's generic manufacturers were cutting the incentive for major drug makers to invest in research and innovation if they were not going to be able to reap the exclusive profits that patents bring.

    "This case is about safeguarding incentives for better medicines so that patients' needs will be met in the future," says Eric Althoff, a Novartis spokesman.

    International drug companies have accused India of disregarding intellectual property rights, and have pushed for stronger patent protection that would weaken India's generics industry.

    Earlier this year, an Indian manufacturer was allowed to produce a far cheaper version of the kidney and liver cancer treatment sorefinib, manufactured by Bayer Corp.

    Bayer was selling the drug for about $5,600 a month. Natco, the Indian company, said its generic version would cost $175 a month, less than 1/30th as much. Natco was ordered to pay 6 percent in royalties to Bayer.

    Novartis says the outcome of the new case will not affect the availability of generic versions of Glivec because it is covered by a grandfather clause in India's patent law. Only the more easily absorbed drug would be affected, Althoff said, adding that its own generic business, Sandoz, produces cheap versions of its drugs for millions across the globe.

    Public health activists say the question goes beyond Glivec to whether drug companies should get special protection for minor tweaks to medicines that others could easily have uncovered.

    "We're looking to the Supreme Court to tell Novartis it won't open the floodgates and allow abusive patenting practices," said Eldred Tellis, of the Sankalp Rehabilitation Centre, a private group working with HIV patients.

    The court's decision is expected to be a landmark that will influence future drug accessibility and price across the developing world.

    "We're already paying very high prices for some of the new drugs that are patented in India," said Petros Isaakidis, an epidemiologist with Doctors Without Borders. "If Novartis wins, even older medicines could be subject to patenting again, and it will become much more difficult for us in future to provide medicines to our patients being treated for HIV, hepatitis and drug resistant TB."

    Related stories:

    • Generic antidepressant pulled off market
    • New AIDS approach saves lives

     

     

    31 comments

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    Explore related topics: india, novartis, generic-drugs, patents
  • 9
    Jan
    2012
    4:57pm, EST

    What you need to know about the Novartis drug recall

    Scott Olson / Getty Images

    Four different Novartis products may contain tablets or caplets from other Novartis products packaged at the company’s Lincoln., Neb. facility.

    In addition, the FDA warned Monday some of Novartis' over-the-counter pills may have been packaged with prescription opioid drugs sold by Endo Pharmaceuticals, which are packaged at the same facility. Those drugs include Percocet, Endocet, Opana and Zydone.

    The FDA says the risk of finding a wrong tablet among the prescription medications is low.

    As for the over-the-counter medications, Novartis has voluntarily recalled all bottle sizes of Excedrin and NoDoz with expiration dates of Dec. 20, 2014 or earlier, as well as Bufferin and Gas-X Prevention products with expiration dates of Dec. 20, 2013 or earlier, in the U.S.

    Consumers who have purchased these products should return them to Novartis for a full refund.

    Contact the Novartis Consumer Relationship Center at 1-888-477-2403 (available Monday-Friday 9 a.m. to 8 p.m. Eastern Time) for information on how to return the affected products and receive reimbursement.

    A full list of the recalled products, below, can also be found on the FDA website:

    Bufferin:

    Bufferin  Extra Strength Tablet

    Bufferin  Low Dose Tablets

    Bufferin  Regular Strength Tablets

     

    Excedrin:

    Excedrin Back & Body Caplets

    Excedrin Extra Strength Caplets

    Excedrin Extra Strength Express Gel Caps

    Excedrin Extra Strength Gel Tablets

    Excedrin Extra Strength Tablets

    Excedrin Migraine Express Gel Caplets

    Excedrin Migraine Caplets

    Excedrin Migraine Gel Tablets

    Excedrin Migraine Tablets

    Excedrin PM Caplets

    Excedrin PM Express Gel Caplet

    Excedrin PM Tablets

    Excedrin Sinus Headache Caplets

    Excedrin Tension Headache Caplets

    Excedrin Tension Headache Express Gel Caplets

    Excedrin Tension Headache Gel Tablets

     

    Gas-X

    Gas-X Prevention Caplets

     

    No Doz

    NoDoz Maximum Strength Caplets

    5 comments

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    Explore related topics: novartis, daily-nightly, novartis-recall, novartis-recalled-medications, novartis-pain-medication, otc-recall

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