Texans Gain the Right To Try Individualized Medical Treatments
Ailing Americans are winning expanded freedom to try experimental medicine.

If you're so sick that you have nothing to lose and you're looking the Grim Reaper in the face, why shouldn't you be able to try experimental and officially unapproved treatments? While libertarians recognize individuals' right to take their own risks, even those of a more nanny-ish disposition have a hard time coming up with answers to that question. That's why the Right to Try movement has taken off across the country, marking its latest victory in Texas.
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Right To Try Chalks Up Another Win
"In a major win for rare disease patients, Texas Governor Greg Abbott signed Goldwater's Right to Try for Individualized Treatments Act," Brian Norman of the Goldwater Institute, which champions right-to-try legislation, wrote last week. "Championed by Senator Paul Bettencourt and Representative Ken King, SB 984 expands Goldwater's original Right to Try law to potentially lifesaving treatments that are designed specifically for individual patients."
Right-to-try laws have been passed in at least 41 states, largely based on model legislation crafted by the Goldwater Institute that allows those with terminal illnesses access to experimental treatments. Colorado was the first to adopt right-to-try, though Texas wasn't far behind, passing such a law in 2015.
Counterpart federal legislation passed in 2018. At the time, President Donald Trump, then in his first term, commented, "With the Right to Try law I'm signing today, patients with life-threatening illnesses will finally have access to experimental treatments that could improve or even cure their conditions."
In 2023, the Lone Star State expanded right-to-try to patients with chronic ailments. That law specified that "it is the intent of the legislature to allow patients with a severe chronic disease to use potentially life-altering investigational drugs, biological products, and devices."
By that time, some states, including Arizona, had already passed laws expanding right-to-try to include individualized treatments that hadn't been contemplated in the original legislation—or even by most physicians, not long in the past.
Reducing Barriers to Tailored Medicine
"Rapid medical innovations have made it possible to take an individual's genetic information and create a treatment for that individual person," notes the Goldwater-sponsored Right to Try website. "More patients, especially those with rare and ultra-rare illnesses, will pursue these treatments when they have exhausted other options. Unfortunately, the [U.S. Food and Drug Administration]'s current regulatory scheme is not designed to handle these kinds of individual treatments, and that will keep life-saving medication out of the hands of patients unless reforms are adopted."
Just days ago, Cincinnati's WKRC marked National Cancer Survivor's Month by highlighting patients who benefited from radiation and chemotherapy treatments that were tailored to their bodies.
"Precision medicine is finding mutations or proteins in an individual's body that suggests that certain drugs can be used to treat that patient not only most effectively but with the least side effects," Michael Gieske, director of the Lung Cancer Screening Program at St. Elizabeth Healthcare, told WKRC.
In Texas, legislation to clear the way for patients to try such treatments before they've been formally approved came in the form of SB 984, which "establishes a pathway by which patients with rare or ultra-rare diseases may seek, under their doctor's care, personalized treatments developed in federally approved facilities."
The bill's sponsor in the Texas Senate, Sen. Paul Bettencourt (R–Houston), boasted, "Texas is again leading the nation in fighting for the most vulnerable patients, whose only hope lies in cutting-edge, individualized treatments not traditional clinical trials, and for me, the coolest thing you can do as a legislator is pass a bill that saves lives."
The Limits of Right To Try
None of these laws can guarantee that an experimental treatment will actually improve a terminal or chronic patient's condition, of course. But there's no good reason for blocking access to promising or even long-shot treatments when patients have run out of other options.
Through the various incarnations of proposed legislation, the Right to Try movement has sought to expand patients' choices and reduce bureaucratic barriers to treatment. But it's not perfect. Right-to-try laws create exceptions to red tape that stands between patients and potentially life-saving treatments, but they don't fully empower people to make their own decisions, nor do they eliminate the bureaucratic hurdles that slow the approval of medicines and medical devices.
"Drug lag costs lives because people suffer and die from disease that might be treatable, if only there were more investment in finding a cure," argued Jessica Flanigan, an associate professor at the University of Richmond, in her 2017 book, Pharmaceutical Freedom: Why Patients Have a Right to Self-Medicate. "Requirements that raise the cost of development make it less likely that they will succeed. Premarket testing conditions also cost lives because patients with conditions that could be treated or cured by unapproved drugs suffer and die while they are waiting for approval."
Flanigan recommends a fully libertarian approach that would remove the restraints from people's freedom to try medications and medical treatments based on their own judgment and the advice of whatever sources and experts they choose to consult. It's a morally good and consistent take that would eliminate the barriers to medicines and medical devices while also lowering the costs of developing new ones. People would be expected to shoulder the burdens of any risks they take.
But liberating though Flanigan's approach would be, it's far more difficult to get through legislatures than are a series of incremental right-to-try laws that erode bureaucratic hurdles a little at a time.
The Next Right-To-Try Frontier
Montana took the next step last month when Republican Gov. Greg Gianforte signed a bill allowing for centers where patients can receive experimental treatments that have completed phase 1 clinical trials but not yet been approved. Everybody is eligible, subject to recommendations from physicians and the requirements of informed consent. To escape federal regulation, experimental meds administered in the centers will have to be produced in Montana—but the state has an active pharmaceutical sector.
Texas took an important step last week toward expanding the right to try experimental medical treatments to a broader sector of the population. But the Right to Try movement isn't nearly done.
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When can we escape the gate-keepers and rent-seeking trolls under the bridges which require us to BUY THEIR PRICEY AND SLUTTY SPERMISSIONS before we do ANYTHING, including scratching our own assholes?!?! There's a slut of delicunt tissues down there, ya know!
Meanwhile, standing by with the trolls under the bridge...
To find precise details on what NOT to do, to avoid the flute police, please see http://www.churchofsqrls.com/DONT_DO_THIS/ … This has been a pubic service, courtesy of the Church of SQRLS!
S/dr
sb,ddtl
It better not include horse paste.
What about bleach?
...
Unfortunately, the [U.S. Food and Drug Administration]'s current regulatory scheme is not designed to handle these kinds of individual treatments,
This is true, but they're deeming them something they're supposed to handle anyway. These are not commercial products, but rather materials used by practitioners in individualized treatments they themselves devise. By regulating them as if they were actual products in interstate commerce (even though each will never be used by more than one patient), the authorities have created a class of articles whose purveyors could never practicably license according to the statutory requirements, but which are required to be so licensed.
A better solution than "right to try" would be either a judicial or statutory constraint on the ability of regulators to deem things articles of commerce when they're really tools used by professionals to ply their trade, which is the real service.
One bit of legislation I've long thought would really help — and not just regarding food and drugs, and not even necessarily only federally — would be to make product disclaimers effective and establish a high bar to rebuttal. That is, a label statement to the effect, "Not to be used for..." or "This is not a...", should be taken seriously in law, and require some explicit statement by the same party to contradict. This would keep regulators from seizing products and saying, "We think you know purchasers are actually using this for...."
But do you think legislators are too chickenshit to adopt such a broad reform?
That would be a good start. The real solution is for the government to just butt out. But that will never happen.
* The do-gooders and sob sisters will use every instance of something going wrong to demand that government step in to protect us from ourselves.
* The public in general, and especially when egged on by the aforesaid do-gooders and sob sisters, will not tolerate kicking people to the curb and saying, "You signed the waiver, now suffer in silence and leave us alone". They will demand some sort of government safety net, and that is how socialism happens. Social Security started as a safety net, and now most(?) or at least a whole lot of retirees depend on it.
* Obamacare is just one more step on the way. I can't see any way to unwind all this. And the more the government provides, the more they feel justified in telling you how to be healthy -- no tobacco, no vaping, no red meat, no meat period, but pot is OK, so are bugs, and so on.
I put the root cause as people having no control over government, so it ends up being better to sic government on everybody else before they sic government on you. Or, since everybody else is getting something from government and no individual can prevent that, better to get your own.
But there's no good reason for blocking access...
FYTW isn't a good reason? 30 years on the job and now you tell me.
- Gov Bureaucrats
My prediction is that this will lead to the creation of the equivalent of oncology chiropractors.
Rare disease patients who need individualized experimental therapy already of access to a limitless number of experimental therapies through compassionate use, expanded access, and clinical studies.
Insurance won't pay for this, so you'll see grandma empty her life savings on snake oil.
And of course only government can save grandma from herself. The judicial system is way too expensive and slow.
Break open the deathgrip the AMA has on healthcare. Next the insurance companies, and we will actually have a free market, and the lowest prices in the world!
Yeah right - Texas is all in favor of people getting medical treatment, unless it's a pregnant woman wanting to exercise her decision to terminate her pregnancy.
Until you can articulate your opponent's point of view, you're just shouting at the sky, virtue signalling to the choir.
Opponent's point of view is that Every HUMAN Sperm is Sacred!!! (Other organisms and orgasmisms can just fuck the Hell right off; who cares about THEM?)
('Cause God told us so!)
It is strange that Texas want to allow terminally ill patients access to experimental treatments, but will not allow care for a failing pregnancy.
Freedom to choose your own medical plan?
The left won't like this idea of choice.
After all, choosing is the exclusive right of our obvious betters in power to choose for us since they're all so much smarter than all us peasants put together.
Indemnification.
If you give express, agreed-to, signed and initialed on all the dotted lines blanket indemnification to literally everyone involved in your Right To Try treatment, then go for it.
Otherwise, not a chance. MedMal suits would go through the roof.
There needs to be mechanism to allow patients greater input into their own medical care, whether that is experimental treatments, full reproductive decisions and the decision to end one life. All of these areas require some government sideboards, but these should be minimal. Rather than discussions of allowing people to make these decisions, I would rather start from allowing them to make the decision and then workback to how government can stop people from being taken advantage of when faced with a terminal illness or a problem in pregnancy. Allow people to get the care they want with the smallest government footprint.