Company Raises the Price of a Drug That Fights Infant Epilepsy by 85,000%
futurism.com
futurism.com
Going off the numbers in the article, MNK sold $1B last year. At $34K/vial that's about almost 12 vials per infant (2,500/yr) per year. (Assuming the course of treatment is one year)
When the vials were selling for $40 each, they would have brought in $1.2MM - I'm no expert, but that doesn't even sound like enough to rent a lab and hire scientists/technicians.
The real headline of this article should be, "MNK settles $100MM lawsuit over anti-competitive drug pricing behavior" (or something more catchy) -- That, to me, is the real interesting bit.
How regulations work around drug pricing is where media focus should be, and there are just as many soundbites in that discussion for the media to latch on to as well.
I imagine the one weird trick they were using to bring down costs is only to devote a small number of days each year to producing the particular drug. It'd be interesting to see the current production costs.
How do you decide what is profiteering, let the courts decide, just pass the law and then pass the judgment to the courts. They will use common law and all the other stuff they have under their belt to make that decision, economic theory and what not.
The point is to get business strategists to understand that there is a risk of bluntly increases prices to make a profit.
I think we need to rethink the entire system. There should be incentives for drug research and discovery, but we still need a functioning competitive market if we expect prices to stay at reasonable levels. One idea is, rather than giving the discoverer monopoly rights, require anyone else who produces the drug to pay a percentage of their production costs as a royalty. This preserves the competitive advantage of the company that discovered the drug, but anchors the consumer price to the cost of production.
The real issue is the cost and length of clinical trials. I know this can be lowered somewhat by allowing computational models, but it is a difficult problem to solve unless biotech goes through the same garage Revolution as the PC
What I mean (very roughly) is something like:
Untested => you are on your own, don't imagine you can sue anyone if something goes wrong, this is the default Conditional => some basic efficacy/safety protocols have been evaluated, some limited liability for the drug companies, Approved => full suite of evaluation done, liability still capped but at a much higher level then Conditional
There would still be legal safeguards around fraudulent or negligent practices of course that wouldn't be constrained by the capped liability I suggested above.
This is a terrible idea. The judiciary is there to adjudicate conflicts based on the law as created through the legislative process. Not to craft their own laws.