India Won't Patent Minor Modifications In Drugs
from the closing-the-loophole dept
While many people are aware of how dangerous software patents are to innovation in the software space, not nearly as many feel the same way about pharmaceutical patents. However, there is increasing evidence that pharmaceutical patents are harming healthcare in a variety of ways, often by slowing the pace of innovation by locking up important concepts and making them too expensive. Recently, India was pressured to update its patent system to cover pharmaceuticals (in many countries, pharma patents are a relatively recent addition), though the rules state that drugs created before 1995 cannot receive patent protection. However, drug makers have long learned that a great way to artificially extend patent protection on a drug is to make a tiny modification and then get a new patent. That's why you now see Clarinex on the market from the maker of Claritin. Claritin went off patent, so the maker came out with Clarinex, advertising that it was much better, even though that doesn't actually seem to be the case.It seems that pharma firm Novartis tried to use this little trick to sneak in patent protection in India for a leukemia drug that came out before 1995. It tried to get a patent on a slightly modified version of the drug, which would then let it ban the sale of generic versions of the non-patented version of the drug. Luckily, as pointed out at Against Monopoly, an Indian court has denied the request, since Indian law says patents should only be granted for new products, or ones where there's a significant improvement -- which is not at all true in this case. That means generic makers can continue to market their drug in India and many, many more leukemia patients will be able to afford the medicine. Novartis, of course, whines that this will slow down drug development, but the evidence suggests exactly the opposite. Having a truly competitive market increases the incentive for real innovation. What Novartis wants is to focus on marginal, useless innovation for the sake of keeping monopoly profits.
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Filed Under: patents, pharmaceuticals
Companies: novartis
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Re: Not certain USELESS innovation is a good busin
Another example is Prilosec vs. Nexium - which confirms Mike's observation.
I had used Prilosec for years. with good results when the patent expired and it became available over-the counter.
Sometime later, my doctor suggested a change to Nexium. It costs quite a lot more because it was new and not available as a generic or over the counter.
Motivated by the higher cost, I read the chemical makeup of the two. Even though I'm not a chemist or otherwise technically qualified to judge, they seemd so obviously similar that I talked it over with my pharmacist.
He whispered (really) - and actually looking over his shoulder - told me that there was no practical difference between them. I continued with over-the counter Prilosec, with the same good results.
If Prilosec is safe enough to sell over-the-counter now, why wasn't the exact same medicine safe enough for OTC sales while the patent was still in force?
Simple - they make more money selling drugs via prescriptions.
That's why they advertise prescription drugs directly to consumers - "ask your doctor if this crap is for you". (it's funny how many times they aren't even clear about what "illness" you're supposed to be suffering from - just ask for a prescription, sucker.)
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Re: Re: Not certain USELESS innovation is a good b
I think Mike made a typo and it should be 'useful innovation'. The big drug companies can then put down patents and make big profits on these innovations. They would thus be generating new drugs, not trying to profit from slightly changed old drugs.
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Re: Re: Re: Not certain USELESS innovation is a go
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Oh yes, innovation is just so easy.
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Patent Law in India
This doesn't make any sense. How can this cause the sale of a non-patented drug to be banned? Have you made a small error of interpretation?
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Re: Patent Law in India
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Re: Patent Law in India
Let's say a company invented and patented aspirin. It now can ban any generic version of aspirin, meaning that any generic version of a drug with the core ingredients of aspirin (hence, what effectively makes it aspirin) is banned.
At some point, patent runs out and the company now "invents" this new aspirin with strawberry flavor and receives a new patent for that. And it can continue to ban any generic version (even generic versions of the previous "version" of aspirin), because this new patent, although it is for the "new" product, it essentially still (or rather again) covers the same medically relevant components.
Basically, these "follow-up" patents are awarded much too easily, when the difference between the original and subsequent version is too small/insignificant
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It's all about business models!
Generic drugs are a useful incentive to get drug firms to innovate and lower costs of non-novel drugs. The answer's simple to be honest, pay for performance ... if a drug is a non-substantial improvement then payors,i.e. insurance firms/governments should only pay a fractional increase on the generic cost (which currently isn't happening).
Drug firms should still be given a premium for truly novel drugs as this is will keep driving innovation!
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Then again, judges have been making some good decisions lately.
Maybe we will get there within my lifetime.
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Patent Law in India
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MAXIDEX DEXAMETHASONE WARNING
Two days later I was BLIND
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Or call 800-757-9195
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