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Was it 'unprofitable' as in 'losing money', or 'unprofitable' as in 'not worth the time'? If it's the latter, I don't have enough information about the rest of J&J to draw any conclusions.
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> Everyone in America who makes <138% the poverty level qualifies for free insurance. qualifies is kind of a weasel word though, "in theory they qualify, in practice ..." I'm guessing this is the US Medicaid system that recently
https://www.theguardian.com/tv-and-radio/2024/apr/15/john-ol...Admittedly that's the UK Guardian reporting on John Oliver which is indeed an auto nope for some, but the issues highlighted here seem real. |
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Indeed, I read the article which was utterly uninformative about what is going on. Can you explain it? As I understand it, Medicaid has waived all ongoing requirements for coverage due the pandemic, and people are now required to verify they still qualify. People who make too much will and do not qualify for Medicaid now need to purchase subsidized insurance on one of the markets. Of course the article does noting to explain what "surprise procedural issues" means. IT seems that the word surprise is an entirely editorial insertion. Based on KFF reporting, it seems that it just means anyone who didnt complete the renewal processes. This includes those that no longer qualify and therefore did not complete complete the renewal process. Of course there is valid concern that some of these people may still qualify and did not complete the paperwork, but it completely unclear how many that is. It could be 0.1% of the 11 million or 99%. https://www.kff.org/report-section/medicaid-enrollment-and-u... |
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Why is it so expensive? because the vast majority of Americans can and will pay it instead of opting for slightly cheaper options. It is a tragedy of the commons with consumers driving up price
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The observation is that companies don't do things that lose money. Or if they do, they run out of money and have to stop. There is no "should" here. Just a description of how the world works. |
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There is no "academic side" of the pharmaceutical industry. There is just academia. And the goal of academia (publishing) are very different than the industry (identifying a new drug). |
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Why does the government allow big pharma companies to “leech” the patent? What does that even mean? Can you describe the steps by which big pharma obtains the patent?
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I'd be eager to learn more, but it seems that they have only published the topline figures [1] and some of their methodology [2]. Details will follow in a journal. Perhaps worth noting that development cost account for more than the phase 2-3 studies and that cost are lower for combinations of known drugs. But yes, 34 million is a lot less than 3 billion. [1] https://msfaccess.org/precedent-setting-move-towards-drug-de... > *Total costs were €33.9 million. While the topline results were presented at the WHO PPRI conference, the full detailed costs of the clinical trial have been submitted for a peer-review publication to a journal. In the full publication, the costs are broken down into 27 cost categories, by year, and by trial site, in order to offer a high level of transparency. [2] https://msfaccess.org/transparency-core-clinical-trial-cost-... |
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This is essentially true. Pharma is incredibly expensive (for lots of different reasons), with R&D taking up a huge portion of those costs. So yes, it's safe to assume that part of the accounting around those published costs in the billions are all of the failed candidates that never even made it to trials (the failure rate varies depending on the area of biology and the type of drug, but it's generally around 9 out of every 10 candidates [1]. By the time you get to trials, that ratio gets even more abysmal). Disclaimer -- I work for Recursion, a company built around this very problem. - [1]: https://www.sciencedirect.com/science/article/pii/S221138352... - [2]: https://www.recursion.com |
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R&D takes lots, but so does compliance --for good reason. But compliance costs a lot of money, directly and indirectly. Lots of people, lots of inefficient processes, etc.
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Yes, universities and public research labs. What they aren't effective at, however, is financing trials, so unless we find a way to overhaul that issue we have to deal with pharma companies.
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Yes. You are the one that's trying to argue that pushing past clinical trials is riskier than fundamental research, so I don't understand your argument. You have to argue that clinical trials are riskier, not that they are risky at all. I suspect we would agree that fundamental research is actually far riskier. Universities and research labs are really quite good at coming up with drugs that are good candidates for clinical trials, so the issue is not an issue of development, it's an issue of aligning incentive and finance to get them to pay for trials, which is not currently possible. This is a problem that is likely solvable. Showing that this is not true would require you to show that private pharmas are somehow able to come up with drugs that are more likely to survive clinical trials, which is not something I believe to be true. There is some evidence on this subject - in fact, a rising percentage of drugs are invented in academia (more than 30% as of 2020), and then transferred to for-profit pharma companies that then run trials, which indicates that academia can produce new drugs more efficiently (see for example https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552459/), and that academic-invented drugs are as likely to succeed even when early trials are largely ran by academic institutions (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226120/) Indeed, recent data shows that a growing majority of biotech drugs are acquired from universities, and in turn those are a growing majority of newly approved drugs - a large and very profitable part of the pharma industry nowadays is to get universities to come up and screen drugs for you, and then to run them to trials. This arbitrage opportunity indicates to me that yes, publicly funded research seems to be a very efficient source of drugs. This is even clearer when you realize that only 20% of public research funding goes towards drug development - most of it goes to the fundamental research that makes it possible to come up with drugs in the first place, something that pharma companies will never do. |
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I'm not arguing against your premise because your conclusion - that you leave implied - doesn't follow from your premise. When your argument did follow from your premise, that "all the expensive parts" is solely in the clinical trial, I did argue against your premise. What you actually wrote in your second comment doesn't effectively argue against my point. There's no point arguing your assertion that clinical trials are expensive, they are, what you needed to argue was that it means that pharma companies are more efficient at developing drugs. It can even be true that clinical trials are more expensive and that most of the aggregate cost from failed drugs is due to those that fail late, as well as that public research is more efficient at developing drugs. Why? Because the likelihood that a drug fails, late of early, is a function of the drug itself - we expect that any trial of the same drug would arrive at essentially the same result. Therefore, even if the total cost of failed drugs is concentrated in those that fail late, that cost mostly has to do with the initial drug design, and I've provided quantitative data on the success rate of academic drug design, which is comparable or better than private drug design. Therefore, the evidence is that academia can actually design drugs that have a competitively low expected cost from late failure. Market dynamics also support this : a major and growing portion of new drug approvals are exactly this : academia designs a drug that has a competitively low cost from late clinical trial failure, a biotech company buys the rights to it after academia makes a compelling case, the trials succeed, and the biotech company makes a large expected profit. So, even if your hypothesis is that most of the cost is from drugs that fail do fail late, it doesn't challenge the idea that academia is good at discovering drugs, because the drugs academia discover aren't more likely to fail late, according to the data I found and provided. Also, you have to show that the majority of cost is from drugs that fail late : that doesn't seem true at all. The total cost of all clinical trials in the US is around 7B$ a year (https://www.clinicalleader.com/doc/considerations-for-improv...). As you correctly imply, this is a cost that is borne in large majority by the private sector. However, the other costs that are borne almost exclusively by the public sector and that are a necessary additional cost to add to the cost of drug development, is fundamental research, which provides new targets and modalities that are a necessary precursor to drug research. That accounts for the majority of the NIH budget, which itself is only one of the institutions that funds such research, and amounts to 48B$. |
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Say I run 10 trials that cost 10m each but only one of these finds a drug that works. How much did the trial cost to discover that drug? How much did it cost to discover that drug? 10m? 10*10m?
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10M. Failure is still useful information so the other 9 trials cost 10M each but didn't produce a viable product, but that doesn't mean nothing of value was gained.
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So like any business. Just because 90% of restaurants fail doesn't mean the cost of running a restaurant is 10x of what it actually takes to run a successful one.
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Sounds like a losing strategy for most customers and businesses Why not pool costs and split profits. Everyone gets less.. less risk, less losses, less profits. |
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Why have only a single winner get the proceeds of getting a winning lottery ticket, when everyone could band together, buy all the tickets, and split the proceeds?
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If their claim is true, should they not do it themselves and make a lot of money? It would help their mission greatly to have a few extra billion dollars.
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The article is mostly not about drug development as a whole, merely the cost of trials. All that is being asked is that the cost of trials be public information.
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You forgot to mention that we can now effectively "cure" obesity with GLP-1 receptor agonists. Oh, and as a nice little bonus they also curb substance use disorder! |
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That's fucked-up and I'm sorry that happened. Clearly things could be much better. But that doesn't mean the system as a whole isn't a huge net positive. The right approach is tweaking, not destroying. |
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In your example, if it did take a programmer 5 minutes, and they don't have any real accountability anyway (not like a real engineer), then why _are_ we paying them so much?
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The cost of manufacturing the drug is only relevant if the drug can be discovered and proved effective by the Magic Drug Fairy. Here in the real world, that manufacturing cost is largely irrelevant. |
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Not particularly, but there really isn't much difference between a generic drug plant and a branded factory. Same machines, same kinds of people, basically all the same.
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Just so I know, is the insulin thing rhetoric or do you not know what happened with insulin? If it's rhetoric, I'm happy to let you have the floor. I'm not one really to kick folks off the pulpit.
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I don't like conversing with people who spend more effort condescendingly implying they're correct than making a point. But I’m not one to chastise if that's how you like to talk. Novolog in 2024 is cheaper than almost any point in the history of (that version of) the drug. "Strangely", Novolog and competition (eg. Humalog) increase prices almost in perfect lockstep, for decades, dramatically outpacing inflation, which is not typically how prices look in a competitive market. Decades after the "cost of research" should be priced in. The obvious reason for this, is that the drug is a medical necessity and consumers can't shop around, so typical market dynamics don't work, allowing companies to raise prices without repercussions. Furthermore, drug companies voluntarily stopping production of cheaper, older, off-patent insulin products - not a single one has been stopped for safety reasons, and clinic benefits of new products since the 1921 patent are minimal. In the 2020s, US politicians started publicly criticizing drug companies for their prices of insulin. Then they introduced a slew of bills intending to cap the price at $35/mo - a 70% reduction. Several bills failed to be passed, but one managed to pass. In that time, all major insulin manufacturers announced they were "voluntarily" reducing their prices to $35/mo (or lower) - set to take affect the same time as the above mentioned law. Not sure how you think the history of insulin technology really relates to this, other than the 1982 recombinant DNA insulin was promised to be cheaper? It doesn't work meaningfully better for most patients. When recombinant DNA insulin ("human insulin") was first sold in the US in 1982, it was priced at $0.5/day (1.5 in 2024), while traditional "animal" insulin was closer to $0.3/day (0.95 in 2024). It was special because it promised unlimited supply, with minimal risk of shortages. Eli Lilly said, in 1982, that they expect the price to drop over time. The first time that it was cheaper (inflation adjusted) was 2024 when the new US law went into affect. Oh, this only applies to the US, elsewhere the prices have been low and dropping consistently, even from Eli Lilly. What's truly damning, is that the clinical benefits of the insulin invented since that first University of Toronto $1 patent version is pretty minimal compared to the UT version from 1921. You can make snide comments of "wading in the shallows" discussing new technology, but the original patent would still have provided comparable medical outcomes to the millions of people who need insulin in 2024. Is it possible you're defending the actions of a giant corporation that raised the prices of a medically necessary drug out of greed, and now you're re-writing history for them to justify your defense? Maybe you need to devise a new self-test to check your belief systems. Citations: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10718803/ Inflation Calculator: https://www.minneapolisfed.org/about-us/monetary-policy/infl... Archival News from 1982 and https://www.washingtonpost.com/archive/politics/1982/10/30/f... https://www.nytimes.com/1982/10/30/us/a-new-insulin-given-ap... |
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Most people don't need Microsoft Office to survive. And, the price of Ozempic is $83 in France. American patients are being outright ripped off, and this is not an isolated incident.
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Interestingly, there are also places to get generic semaglutide. I'll admit to some interest in the idea myself, but so far I've not been willing to roll the dice on that process.
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Actually, last year the NIH budget was $48B, 4/5ths of that went straight out as grants for research, and another 11% went to internal labs:
https://www.nih.gov/about-nih/what-we-do/budget And you have to be very careful about what counts as R&D, for example Merck reported $30B in R&D, but one half of that was actual for mergers and acquisitions (of research related companies). I have yet to find anyone who has good numbers on this, which is why the study in this article is interesting: it sounds like the article is going to be very transparent about what it means. And for absolute candor here, you have to remember that once the NIH grants arrive at a university somewhere between 15% and 60% (really, it varies wildly) is taken off the top for University expenses, some of which are related to the research (e.g.: building costs), and some of which are not (arguably: university administration). |
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But they need these huge margins to pay for the politicians and media coverage (or absence thereof) that allow them to do what they do.
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They stop making it, and pay generic manufacturers not to. https://www.nbcnews.com/business/business-news/drug-firms-st... > Known as "reverse settlement payments," or "pay-to-delay" deals, the financial arrangements are a unique but common practice in the pharmaceutical industry. Essentially, they allow drug manufacturers in some instances to pay competitors not to manufacture generic versions of their products, thereby ensuring that they maintain patent protection for as long as possible. |
Worth noting as well that J&J have shut down their entire division in communicable diseases because it was so unprofitable for them.
(Source: I work in this industry)