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Medicine Communications

New Startup Hopes to Push Open Source Pharmaceuticals 101

waderoush writes "Nothing like the open source computing movement has ever caught fire in biology or pharmaceuticals, where intellectual property is king. But drawing inspiration from the people who make Linux software, and the social networking success of Facebook, Merck's cancer research leader has nailed down $5 million to launch a nonprofit biology platform called Sage, which aims to make it easier for researchers around the world to pool their data to make better drugs. 'We see this becoming like the Google of biological science. It will be such an informative platform, you won't be able to make decisions without it,' says Merck's Eric Schadt, a co-founder of Sage. He adds: 'We want this to be like the Internet. Nobody owns it.'"
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New Startup Hopes to Push Open Source Pharmaceuticals

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  • i've found that there is plenty of pull, no need to push.

  • I can hear it now: "We need these open-source drug pushers off our streets!"
    • can hear it now: "We need these open-source drug pushers off our streets!"

      These guys are too late. The CIA [google.com] already did this with LSD!

    • and out of our inboxes! Can't forget that one. I mean everyone's thinking meth labs but do we really want the recipe and process out there for some prescriptions so people can make them in their basement and try and sell em online with the same stupid tactics we see today? I don't think the FDA would approve Billy Bob's Basement Joint Care Medicine - "made with open source information"
  • make it easier for researchers around the world to pool their data to make better drugs.

    As in, like, paying them lots of money? No? I don't see this ever getting off the ground. And, uh, ask Proctor and Gamble what $5 million will buy you.

    • Re: (Score:2, Insightful)

      According to your ideas, then, Linux would have never got off the ground and yet here we are.
      • According to your ideas, then, Linux would have never got off the ground and yet here we are.

        Bad analogy. Linux is information technology; Sage is drugs. National governments regulate drugs much more heavily than IT.

        • by Trails ( 629752 )

          A good analogy. Linux is IT, Sage is data collection and sharing.

          What I'm trying to find, and more relevant, is if Sage's open source license will be "viral", à la GPL.

  • $5 million?

    That will be burnt up in a single clinical trial.

    • by AliasMarlowe ( 1042386 ) on Monday March 02, 2009 @05:21PM (#27044675) Journal
      Intellectual property may be king, but the lawyers are queens (pardon the expression), and their games are hideously expensive. You can't get into the legit end of the drugs business without a strategy for covering legal liability. You should budget at least as much for this as for clinical trials or production facilities. $5M is peanuts in this game.
    • Re: (Score:2, Informative)

      by jackchance ( 947926 )
      Sage is not a research project, it will not conduct trials. it is a data-mining project. They idea is simply to create a standard API so that all the current research will be more effective. The $5M is just to get the thing off the ground. As soon as it has a single success, the funding will flow like water.
  • by Anonymous Coward on Monday March 02, 2009 @05:11PM (#27044553)

    You mean like when research was in the domain of the university, and when science was done by building on the prior work of others? The big dollar companies siphoned away the talent from universities and went patent crazy. They're the ones that started this in the first place.

    The same can be said for internet technologies - people forget that fundamental web technologies such as web browsers and LDAP came out of university research, not out of the big companies or the major standards bodies.

    • by Daniel Dvorkin ( 106857 ) * on Monday March 02, 2009 @05:56PM (#27045097) Homepage Journal

      Shhh! You're not supposed to talk about science and the sharing of knowledge! You see, these days it's all about Innovation(tm). Nobody's sure exactly what Innovation(tm) is, but we know it's heavily dependent on Intellectual Property(c) and it's vitally important that Intellectual Property(c) be Protected(r). How else are we going to synergistically leverage our core assets to maximize stakeholder value?

      • by LynzM ( 1240854 )

        I'm dying over here... only because what you just said could have come verbatim out of my company's quarterly newsletters. It didn't used to be like this, there...

      • by jc42 ( 318812 )

        Nobody's sure exactly what Innovation(tm) is, but we know it's heavily dependent on Intellectual Property(c) and it's vitally important that Intellectual Property(c) be Protected(r).

        Actually, it's fairly easy (now that we have google as a research aid) to make a sampling of the use of the word "innovation" and determine its meaning:

        innovation (n.): Making small, mostly cosmetic changes to someone else's product, then marketing it as an important new development, while suing the producers of the earlier prod

  • This is a very cool idea, but the stakes are a bit higher. I'd think there's going to be significant push-back getting used to the idea of drugs coming from a bunch of guys in their garages. It's sort of like if open source software started designing software for nuclear power plants.

    Then again, maybe people are just so sick of drug prices...

    • Re: (Score:3, Insightful)

      by Jurily ( 900488 )

      drugs coming from a bunch of guys in their garages

      As long as experts contribute, there shouldn't be a problem. Maybe a registration with credentials would be good.

      Software is special, in that all the hardware required is now commodity, and all the knowledge can be accessed fairly easily. At least, you won't see $300 biochem labs from Dell.

      • Re: (Score:3, Insightful)

        by Hordeking ( 1237940 )

        drugs coming from a bunch of guys in their garages

        As long as experts contribute, there shouldn't be a problem. Maybe a registration with credentials would be good.

        Minor problem. Who gets to determine that some researcher isn't an expert, as opposed to that biochem college dropout who knows what he's doing, as opposed to the well meaning schmo whose job is construction, but he knows some folk remedies, as opposed to a methamphetamine dealer whose knowledge of how to brew some rocks is exceeded only by his stupidity in smoking around ether?

    • by mea37 ( 1201159 )

      I don't see that anything these guys do WRT building an information platform is going to change the regulatory environment or layers of process (and expense) involved in actually bringing a product to market. So I'm not concerned about public perception of safety... but it does raise a different issue.

      So this platform provides the basis for a new drug, and "nobody owns the IP" (sort of); ok, that means nobody gets the lock-in of being the one and only brand manufacturer of the drug for a few years after i

      • Right now we know the human genome and that it's about 99% the same for everybody; if we know what the genetic differences are between people with cancer and those without, the differences in which genes are active, what the mRNA and proteins are doing, then we can attack the disease through those differences. Knowing the differences is just a stepping stone to creating safe and effective medicines, big pharmaCos are still going to be able to make money their old fashioned way with this data.

        Even now anybod

      • by Draek ( 916851 )

        Just a question then: how do generics get made and sold? do they get a "free pass" from all that expensive regulation?

        Plus I've always been told that the brand-name pharmaceutics are priced as such to pay for the billions being spent on research, and if a bunch of academics is willing to do that for free companies willing to make it shouldn't need Big Pharma pricing to get a nice profit, would they?

        • by mea37 ( 1201159 )

          Well, I can give a definite answer to one of those, and can only speak generally to the other.

          A generic isn't so much a "new drug" as it is another manufacturer's vesrion of an existing drug. When the existing drug's patent expires, it's already through FDA approval, so generic manufcaturers can more or less pick it up and run with it as long as they follow certain rules about generic equivalence. (There are a couple different classes of generic, but the short form is "same active ingredients in the same

    • "I'd think there's going to be significant push-back getting used to the idea of drugs coming from a bunch of guys in their garages."

      How about from a bunch of guys working in a warehouse in one of the bad parts of town? I ask in all seriousness because a friend of mine is doing exactly this in a biotech startup and apparently attracting venture capital hasn't been too rough. Sure I kid him about being in the drug business on the bad side of town but nobody will ever really know if something looks promi
  • Oh, please. (Score:5, Insightful)

    by chill ( 34294 ) on Monday March 02, 2009 @05:14PM (#27044581) Journal

    Next thing they'll be telling us is we could GROW our own medications in gardens. Medicine and pharmaceuticals are *hard* and require a lot of big government seed money, research, lobbyists, more money, more lobbyists, advertising, etc. The idea that you could grow, say a drug to suppress inter-ocular pressure in glaucoma patients, or a nausea-suppressive for chemotherapy patients is patently absurd! I mean, what next? Analgesics from tree bark?!

    Hippie, commie, open-sourcers will never learn.

    • Re:Oh, please. (Score:5, Informative)

      by dkleinsc ( 563838 ) on Monday March 02, 2009 @05:28PM (#27044759) Homepage

      Next thing you know you're going to be suggesting that ordinary herbs are perfectly good for helping people sleep [wikipedia.org] or combating migraines [wikipedia.org] too.

      Hippie, commie, open sources will never learn indeed.

    • We all know that Merck is one of the last stands of hippie communism, of course...
    • because I'm in pharmacy.

      Many drugs DO come from natural sources. example:
      Pilocarpine [wikipedia.org]: glaucoma drug "obtained from the leaves of tropical American shrubs"

      Of course you couldn't extract and purify the compounds yourself. No one has a lab in his basement. Right??
      • Why, just smoke a joint every once in a while and forget the lab.

      • This turned into a book. Sorry. This post lacks citations and specifics for reasons that should become clear. A full-fledged fully-stocked bioengineering lab isn't really necessary. A high school chemistry lab would be overkill for most of it. Most plant extractions can be done with nothing more than an acid (hydrochloric preferred), a base (sodium hydroxide preferred), distilled water, a separatory funnel and a set of mason jars. Some extractions might further require a bunsen burner, while others might
        • Re:I get the joke (Score:4, Interesting)

          by zeropointburn ( 975618 ) on Monday March 02, 2009 @08:27PM (#27046617) Journal

          Noob mistake and karma burn. I forgot to post as plain text. My apologies.

          This turned into a book. Sorry. This post lacks citations and specifics for reasons that should become clear.

            A full-fledged fully-stocked bioengineering lab isn't really necessary. A high school chemistry lab would be overkill for most of it. Most plant extractions can be done with nothing more than an acid (hydrochloric preferred), a base (sodium hydroxide preferred), distilled water, a separatory funnel and a set of mason jars. Some extractions might further require a bunsen burner, while others might require an alternate solvent such as ethyl alchohol. A blender and a freezer is helpful.

            Anyone that has passed a lab course should be able to extract aspirin (and a bunch of other chemicals) from willow bark in their kitchen. Purifying it down to a single active ingredient is much more complex, but that step is often unnecessary. Provided the plant has no materials with higher toxicity than the sought-after chemical, a simple extraction can be done relatively easily. It takes at least a week (without good equipment), usually more like 4 weeks, so this isn't a 'pick that from the garden and extract' process.

            Actually purifying these extracts is generally either a crystallization or gravity separation process (or both), both of which can be greatly enhanced by the appropriate solvent or by the use of a centrifuge. There are some plants that contain other, unwanted toxic materials with similar physical and chemical properties. This is where the difficulty level starts to ramp up. If you know what you are doing, you can cause either the desireable or the undesireable substance in solution to react and precipitate out, then continue the refinement as normal. All that is required here is access to the appropriate reagents and an understanding of which chemicals to use (in addition to lab process familiarity).

            A person could become competent at all of these processes given a few hours' training and a guidebook with specific instructions. It would be no more difficult than passing a Red Cross first aid test. They would not be chemists, but they would be able to make useful medicinal plant extracts. Of course, this would never happen. The same skills allow access to a number of interesting compounds which are illegal, where the source plant is not (due to proliferation).

    • Re:Oh, please. (Score:4, Interesting)

      by garett_spencley ( 193892 ) on Monday March 02, 2009 @06:19PM (#27045349) Journal

      Well, we will never know how truly hard and expensive medicine is, since there's enough regulation in the industry to make new entry very difficult.

      Of course drug research is expensive when you need to a) make sure your research is patented enough so that you have the exclusive rights to anything and everything that you research and b) make sure that you're complying with the expensive government regulations. Regulations that are pennies for a mega-corp but prohibitively expensive for a new start-up.

      It's also common procedure for any big corporation to pay top dollar for retired politicians to lobby government in their in their favour. To regulate in ways that make it profitable for the existing corporations at the expense of everyone else.

      Human history is full of small groups of researchers, not connected with huge pharmaceutical companies, who made important discoveries in medicine. From penicillin to the polio vaccine.

      • Don't forget biologics (using proteins instead of small molecules: read UCSF/Genentech) and siRNA.
      • My guess is that anything Merck would find useful (patentable) they would patent, and leave the rest for this open source project. GSK is doing a similar practice. Part of the motivation is to encourage development of drugs for neglected diseases, that is, diseases where the market is small and big companies like Merck and GSK have no desire to drop the millions to develop the drug that wouldn't help that many people, or would only help poor people.
    • by Hatta ( 162192 )

      Next thing they'll be telling us is we could GROW our own medications in gardens.

      You could, if it weren't illegal.

  • by CrazyJim1 ( 809850 ) on Monday March 02, 2009 @05:14PM (#27044583) Journal
    If you believe in Sesame Street for kids, you should be interested in online education for adults. The reason why you can't do every subject known to man on television is that there is only limited air time and people would be uninterested in stuff they already know. But you can make an online education school which has videos of lectures for every level of education. Throw in some tests and written course(book) work, and you can guide people through education if they have the drive. You put in a lot of redundancy so there are many ways of looking at the same subject matter if it doesn't click with the student asap. And then you have a pay service where you can ask a teacher question through IM or email.

    I don't know how to start this though. I considered being a jerk and just linking everyone's educational videos on a site that is just a giant index to start... But I don't want people complaining that it is their Intellectual property. The task is too big for me to tackle alone because even though you only have to make a years worth of videos one time for a subject, it still takes a lot of time to do this. To make an online education school with videos would take a lot of work, but I think it'd be worth it for society. Anyone have ideas on how to start something like this?
    • Re: (Score:1, Informative)

      by Anonymous Coward

      Although something of the scope that you describe certainly does not exist yet, there are projects along those lines. The main such projects I know of are MIT's OpenCourseWare [mit.edu], which apparently has spread to some other universities (Wikipedia page [wikipedia.org]). In a similar, but currently much smaller project, Cornell has begun putting videos of some lectures online [videonote.net], but it appears to be only for Cornell students. Hopefully that will change.

      Getting away from just college-level materials, there are a lot of collections

      • Thanks for your information. I'll have a look at some of that stuff especially the free text books. The price of free is the development time, but the rewards are invaluable when complete.
      • i forgot about MediaWiki's WikiBooks... i suppose the smart thingto do here is generate a WikiSchool.org that incorporates wikipedia and wikibooks materials, along with hosted educational vids, into a curriculum to be followed by those seeking educational enrichment.

        then those courses could seek qualification as accepted by the board of education, and a third party org could be developed--like WAVA.org--to monitor and provide proof of the success of students (accreditation of materials/course structure and

    • there are how-to sites out there like this... find one thats free, as in open-source and non-profit, and encourage them to organize not only how-to PDFs and Vids, but quarterly class curriculum as well.

      i homeschool my kid via WAVA.org, a washington state public school that uses K12.com materials... it's really the best way to teach a child, by far... so long as there's a learning coach with the patience to teach the child daily, for free. anyhow, there's no reason a sustainable non-profit version of k12.com

  • Drug Testing (Score:2, Insightful)

    by Anonymous Coward

    A major expense in the development of pharmaceuticals is the testing and approval phase. Only wealthy entities like corporations or governments can afford it. I don't see how the open source concept can get around that problem.

    • It's easy. The big drug companies can fund the trials if they want to manufacture and sell the drugs. They can't patent the drugs if they get the research from someone else. The big question is whether the big drug companies would rather invest in the research and reap the reward of an exclusive market or if they'd be willing to fund trials and sell the drugs if they have to share the sales but also share the expense of research.

      • Re:Drug Testing (Score:5, Interesting)

        by Rich0 ( 548339 ) on Monday March 02, 2009 @05:49PM (#27045023) Homepage

        Drug research isn't actually all that expensive (as in generating concepts). What is expensive is drug development - which is working a concept into a drug candidate and then putting it through trials.

        I suspect that what will happen is that drug companies will look at the breakthroughs in these open consortiums and then develop candidates and patent them and run them through trials.

        Example - the "open source" consortium discovers that inhibiting enzyme A cures cancer. Now, you can't patent the idea of inhibiting enzyme A. However, you can patent molecule 123 as an inhibitor of enzyme A. Somebody else could of course come up with molecule 456 which does the same thing but is a different molecule entirely. That's what we call a me-too drug and it is the reason why people with drug allergies don't die of diseases (they can take a me-too drug instead), and the reason for marginal improvements in classes over time (maybe molecue 456 is slightly better than 123).

        However, once the company proves 123 is safe, they own the market until soembody else comes out with another drug. 123 is after all patent protected.

        Consumers still win because maybe 456 comes along a year later and prices drop as they compete.

        The issue at big drug companies is that they're having trouble coming up with breakthrough ideas for new drugs. The market doesn't need another statin that works 3% better than the 14 that are already on the market. However, something novel would certainly be both profitable and beneficial to the public. So, drug companies are trying to fund more novel R&D. Once some concepts worth developing come out the big pharma companies are experts at running molecules through the process, and after a few hundred million dollars spent getting something on the market.

        This is also smart as the expensive part of drug development is the development part. You're not going to find poorly-funded researchers contributing much to that part of the puzzle. However, the blue sky research component needs ingenuity more than money - and that is what things like this are good at.

        It is an interesting concept - I wonder how it will work out...

        • by tmosley ( 996283 )
          A me too drug is more like a drug number 124, with some part of the molecule that doesn't interact with the site of interest is modified to give you TECHNICALLY new molecule. Patent is submitted, media machine is spun up, and your NEW purple pill hits the market, with the exact same effectiveness and side effect profile as the last one.

          If it were an entirely different compound, it would just be another drug that treats the same problem. It might even do it in a different way.
          • by Rich0 ( 548339 )

            A me-too drug by definition has the same mechanism of action. For example, even though insulin and metformin both lower blood sugar one is not considered a "me-too" of the other since they have completely different mechanisms and potential uses.

            Most me-too drugs usually aren't trivial variations on existing drugs. Sometimes antibiotics fall into this category (often to defeat some resistance mechanism).

            I would think that a drug that is only a trivial variation of an existing drug would be risky from a pat

  • Authentication (Score:3, Insightful)

    by DoofusOfDeath ( 636671 ) on Monday March 02, 2009 @05:17PM (#27044625)

    If one gathers data from many sources, in order to justify to the US FDA some claim about a drug: how can one certify that those data are accurate?

    I was under the impression that despite its horrific flaws, the current regime requires the drug researchers to seriously vouch for the (subset of) the data they present to the FDA.

    • Re: (Score:3, Interesting)

      by mr_mischief ( 456295 )

      There was just recently a case in which the FDA quit accepting applications for approvals from a company. That company was found to be tainting studies, and was the only source of data for the drugs they wanted approved. See bio-medicine.org [bio-medicine.org]'s coverage of that news item.

      If you have multiple sources and most of them are reputable, are you better or worse off than having one source with a unique incentive to put their own drug in the best possible light?

    • "I was under the impression that despite its horrific flaws, the current regime requires the drug researchers to seriously vouch for the (subset of) the data they present to the FDA."

      Just like suing customers does not help the recording industry, killing customers is not in the best interest of the pharmaceutical companies.

      There may be something to be said for drugs that treat HIV/AIDS, cancer and other diseases where the patient needs to be on medication for many years. There is also something to be said f

    • by glwtta ( 532858 )
      If one gathers data from many sources, in order to justify to the US FDA some claim about a drug: how can one certify that those data are accurate?

      No, you gather data from many source to formulate the hypothesis that allows you to make that claim - to justify the claim to the FDA you do clinical trials as per usual.
  • While I hope this works I have a hard time picturing the outcome not being tarnished, influence, and wrecked by profit. Like so many facets of R&D, the people doing the work are being paid to do so and the people doing the paying don't want to share.
  • by Daniel Dvorkin ( 106857 ) * on Monday March 02, 2009 @05:36PM (#27044883) Homepage Journal

    Open access journals such as those from BMC and PLoS, databases such as those at NCBI and EBI, software repositories such as Bioconductor and the Open Bioinformatics Foundation projects (Bioperl, Biopython, etc.) If Sage can take it to the next level, good for them, but I'm not sure I see how one group is going to accomplish this. I suspect it will have to happen more, um, organically, the way open access publication and biology-targeted OSS have.

  • by Ungrounded Lightning ( 62228 ) on Monday March 02, 2009 @05:43PM (#27044959) Journal

    When I saw the title I thought "How the HELL can you have 'open source pharmaceuticals' in a legal regime where new drug compounds are illegal by default?"

    Then I read TFA.

    This has NOTHING to do with making "open source pharmaceuticals". This is about sharing data among drug companies and doctors to try to get a better handle on things like:
      - understanding the gene-regulation changes that occur in major diseases
      - designing better drugs using this data
      - customizing drug therapies by selecting drugs that are a good match for a patient's genetics and disease, picking those that will be safe and effective for him in particular while avoiding those that would cause dangerous side-effects due to his particular genetics.

    It looks like it will run afoul of HIPPA unless it's very carefully designed.

    BAD article title. No donut.

    • Re: (Score:3, Interesting)

      HIPAA (not "HIPPA") doesn't have to be a barrier to sharing research data -- take a look at the U. of Pittsburgh's Honest Broker System [nih.gov] for a very nicely put-together, largely decentralized method of moving data around while staying well within privacy guidelines. Financial interests are a much bigger obstacle to the free exchange of knowledge than are even the strictest regulations.

  • I will be interested to see where this goes.
  • Bob Dylan's "Everyone Must Get Stoned" will become the theme song for this movement.
    • Bob Dylan's "Rainy Day Women #12 & #35." will become the theme song for this movement.

      Fixed that for you.

  • by Adam Hazzlebank ( 970369 ) on Monday March 02, 2009 @06:10PM (#27045247)

    Nothing like the open source computing movement has ever caught fire in biology or pharmaceuticals

    Informatics for Biology... Bioinformatics. Is RUN by open source software. BLAST http://en.wikipedia.org/wiki/BLAST [wikipedia.org] ,one of the most important Bioinformatic tools ever written, is public domain. It's paper is one of the most cited of the past 30 years http://archive.sciencewatch.com/sept-oct2003/sw_sept-oct2003_page1.htm [sciencewatch.com] . Bioinformatic clusters almost universally run Linux. Almost all popular tools are written by academics and supplied under open source licenses. To the degree that I'd say closed source software finds it hard to break in to this area, not the other way round. This is not only true of Bioinformatics, but also large scale Protein simulations. Namd p://www.ks.uiuc.edu/Research/namd/ is also available under and open source (though more restrictive than GPL or BSD license). And is one of the most popular Molecular Dynamics codes available.

    • by Hatta ( 162192 )

      It's a real shame, there's a big gap in the open source bioinformatics tool kit. There's no open source sequence analysis software that can conveniently do things like retrieve genbank entries from the NCBI, retain all features, search for primer sites and restriction sites, and then draw a map of it. There's none that you can use to simulate a restriction digest and ligation for in silico subcloning.

      I've been using Vector NTI for this, and it sucks, but it's free (as in beer) for now. Later this year, t

      • by fotbr ( 855184 )

        Three options:

        A) You pony up for a license, like they want.

        B) You find something else and pay for a license.

        C) You figure out some way to get some funding together - I'd suggest a university with good contacts in the so-called "science-friendly" Obama administration (Its only been a few weeks, we'll see how science friendly this administration turns out to be) and put together a better open-source alternative.

        Either way, the tool has limited use, so it will require money, even for the "free" options.

  • What's interesting about this (I think) is that they're trying to open up research data that usually gets discarded or hidden. They're not necessarily talking about clinical trials of drugs in the FDA approval process. There's lots to be learned from the effects of drugs on various cell or tissue types at various stages of disease or age or any other variable of interest.

    If a research group is studying the effects of compound A on some disease (atherosclerosis, for example), they might use a microarray stud

  • hobbyist computers: couple hundred bucks
    hobbyist biochemistry: millions of dollars

    penalty for screwing up a computer project: reboot
    penalty for screwing up a biochemistry project: chemical pneumonia, sterility, cancer, death, homeland security minions tossing teargas canisters into your window and barking orders

    once upon a time, you needed a studio system to make a movie. now a teenager can make a feature length HD movie with his friends. nothing remains too difficult and too expensive forever, and someday,

  • Screw this idea. I just want a few million people to pressure the FDA to make more known drugs over counter drugs rather than requiring a doctor visit. My kid had strep throat last week. My wife has it this week. We'd much rather go to walmart buy what ever the antibiotic or box labeled take this for strep throat rather than the system we have now.

    For new drugs or unknown experimental crap our existing system is great. For getting drugs away from requiring doctors and where any mom can decide to buy it and

    • Re: (Score:3, Interesting)

      by robkill ( 259732 )

      Very Simple,

      If antibiotics are over-the-counter, then they will be over-used, and/or misused in ways that lead to more antibiotic resistant strains of bacteria (e.g. penicillin-resistant gonorrhea, or MRSA [wikipedia.org]). Shelf life is another concern. Several common prescription medicines not only become ineffective as they age, but eventually become toxic. OTC interactions with prescription drugs are a common problem that would spread as more medicines are made OTC. Too many people take dosage and usage directions

    • We'd much rather go to walmart buy what ever the antibiotic or box labeled take this for strep throat rather than the system we have now.

      The level of insight and understanding in this sentence demonstrates beautifully why antibiotics should never, ever, ever be OTC.

  • Not to be confused with the non-profit maths platform, also called Sage [sagemath.org].

  • by Herkum01 ( 592704 ) on Monday March 02, 2009 @07:52PM (#27046305)

    I wish they would invest more time in making available drugs that have already had their patent expired. I am not talking about stuff that expired yesterday, I am talking about stuff that been out for years but the market is too small for a large company to invest in it.

    I forgot the name of the drug, but it was a cheap drug that served a small market, but it very vital. It was being produced cheaply for years from one factory that served the whole market. Somebody bought it and then jacked up the price by 100 fold. Why? Because no one was going to bother with drug that had such a small market share, but it was critical the people who depend on the drug.

    Someone tell me what the drug is? I believe there was an article in the NY Times a few years ago about it.

    • by Atario ( 673917 )

      Vital but unprofitable? Sounds like a job for The People -- which is to say, government.

  • Doesn't the NIH already do this with Entrez [nih.gov] ? Plus there are plenty of data generating institutions that actually chave such infastructure such as Connectivity Map [mit.edu], Chembank [harvard.edu] and the personal genome project [personalgenomes.org] to name a few. From the article I'm having trouble seeing how "Sage" will offer anything unique.
  • After all, the idea of open source (FWIK) was wanting something important to come in to being *more* than wanting to make a profit from the process. How many people have spent countless hours doing this so they could have an OS or DB that put "working well" before "being profitable"?

    It seems to me that being treated or cured of a painful disease or condition ought to be right up there with not having to use closed source software (some would say I'm being redundant).

    Drug companies are *companies*. Their fir

  • 'We want this to be like the Internet. Nobody owns it.' I think he means 'We want this to be like the Internet, where people sell DRM'd information.'

    Wikipedia, perhaps, would've been a better comparison.
  • Don't opensource drugs exist already, aren't they called generics?

    Some company could develop DRM'd drugs that check the colour of the box they are in.

    If its plain white, you're screwed.

  • As we learn from this rather poorly written article over at xconomy, "Biology has never really had a social-networking movement like open-source computing, where thousands of loosely-affiliated people around the world pool brainpower to make better software". If you translate that into what was needed for biology (or chemistry) according to the xconomy author, it would translate into a "social-networking movement where thousands of loosely affiliated people around the world pool brainpower to make better bi

Our OS who art in CPU, UNIX be thy name. Thy programs run, thy syscalls done, In kernel as it is in user!

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