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The million-dollar drug (2018)

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Re: The million-dollar drug (2018)

#21

I can’t imagine how hard it must be for the dozens of people out there suffering from this rare ailment knowing a perfect cure/treatment is possible but not worth it for the shareholders.

In a world with nothing to loose I am surprised one of those people doesn't go John Q.

Re: The million-dollar drug (2018)

#22
post #19
post #12

It seems to me that it’s not just the price of a single treatment that is too high, but also that the patients are fully recovered and don’t have to pay a recurring annual subscription fee to live normal lives. Or is that too cynical?

Doesn't it say 10 years? So you'd need a few more during your life

No that is not what they implied just that so far it has only been 10 years. These people are still healthy but the company can't say it lasts 30 years because no one has lived long enough to see if it does. It may last indefinitely.

Re: The million-dollar drug (2018)

#23
post #12

It seems to me that it’s not just the price of a single treatment that is too high, but also that the patients are fully recovered and don’t have to pay a recurring annual subscription fee to live normal lives. Or is that too cynical?

Or is that too cynical? My, you innocent child, that you have to ask this. (I have a genetic disorder commonly treated with one of those drugs that cost $300k annually.) Edit: I was going to delete this in short order but now that it's flagged, I'm leaving it. People with genetic disorders get all kinds of hatred from the world and medical system for just wanting to be healthy and how dare we say that online.

Discussing the value of a human life, and figuring out how much the many are willing to sacrifice in order to treat the needy few, isn't something that should be out of bounds.

I don't think the voices of the few should be silenced.

Its uncomfortable maybe, but I think not a discussion to avoid.

Re: The million-dollar drug (2018)

#24

Earlier quoted context omitted.

Or is that too cynical? My, you innocent child, that you have to ask this. (I have a genetic disorder commonly treated with one of those drugs that cost $300k annually.) Edit: I was going to delete this in short order but now that it's flagged, I'm leaving it. People with genetic disorders get all kinds of hatred from the world and medical system for just wanting to be healthy and how dare we say that online.

Discussing the value of a human life, and figuring out how much the many are willing to sacrifice in order to treat the needy few, isn't something that should be out of bounds. I don't think the voices of the few should be silenced. Its uncomfortable maybe, but I think not a discussion to avoid.

[deleted]

Re: The million-dollar drug (2018)

#25

How long does the patent last? It should be made available as a generic drug when the exclusivity period elapses, right?

They usually last around 10 years with some options to extend for another 5-10 years.

By the way, that's one of the reasons drugs are so expensive: pharma co. needs to recoup the costs before the patents expire.

Re: The million-dollar drug (2018)

#26
post #21

I can’t imagine how hard it must be for the dozens of people out there suffering from this rare ailment knowing a perfect cure/treatment is possible but not worth it for the shareholders.

In a world with nothing to loose I am surprised one of those people doesn't go John Q.

Or alternatively, try to hire some chemistry grad students to make some.

Re: The million-dollar drug (2018)

#27
post #21

Earlier quoted context omitted.

In a world with nothing to loose I am surprised one of those people doesn't go John Q.

Or alternatively, try to hire some chemistry grad students to make some.

That might be surprisingly feasible.

https://www.resetera.com/threads/guy-cures-himself-of-lactos...

Re: The million-dollar drug (2018)

#29
post #16

Never mind non-practicing entities for software patents, but surely for patents on medicine keeping them valid when no one is making any is entirely bogus and not deserving of legal protection?

If you invalidate people’s patents for trying to sell their drug at a price high enough to recover R&D costs, they’ll just stop doing R&D for any drugs that will have niche target populations.
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