“If you think research is expensive, try disease.”—Mary Lasker (NIGMS, 2011)
If any medical field needs help, it’s chronic pain. It’s remarkable, indeed, that the treatment options for a field that affects so many and has such huge economic and human costs still largely rely on opioid drugs, most of which were developed decades ago.
The 2011 Institute of Medicine Report, “Relieving Pain in America“, showed just how estranged institutions like the National Institutes of Health (NIH) can get from the needs of the public. The report stated that as the economic costs of chronic pain – which do not include medical costs – reached $530-650 billion a year in the U.S., the NIH was spending less than 1% of its budget on basic pain research.
Not only was the study of chronic pain vastly underfunded at the NIH, but it was being done in NIH’s rather typically haphazard manner; i.e. there was nothing even resembling a strategic plan. Insights were being produced, but the NIH was clearly not treating chronic pain seriously.
In response to the report, the NIH slowly increased funding for chronic pain; six years later, it had increased by about a third. It was not enough. With the opioid epidemic in full swing, Congress jumped in with the HEAL (Helping to End Addiction Long-term) Initiative – adding about $2 billion over the next four years to the chronic pain and opioid research pie.
HEAL’s goal was to end the opioid epidemic – not end chronic pain – two different, but closely overlapping, goals. From assessing how chronic pain is treated in rural areas, to developing drugs to tackle addiction and prevent overdoses, to safe needle and recovery programs, the initiative funds many things that won’t move the needle on fibromyalgia. One of its core responsibilities – finding better and safer drugs for chronic pain – is right up FM’s alley, though.
A Daunting Task
Nothing is easy about developing a good pain drug. Indeed, it’s probably one of the most daunting tasks in all of pharmacology. (Cancer appears to be far easier). We know that’s true because a good chronic pain drug would reap simply huge financial dividends for any company that could develop it, yet most people are still relying on the opioid drugs that were developed decades ago.
The Gist
- The 2011 IOM report on “Relieving Pain in America” highlighted both the terrible toll that chronic pain takes in America and the limited resources the NIH was devoting to understanding and finding treatments for it.
- Skip forward 7 years and the Congressionally funded HEAL Initiative to combat the opioid epidemic and develop safer, more effective pain drugs – perhaps the most difficult pharmacological challenge the drug industry faces.
- The HEAL Initiative brought a much-needed strategic approach to combating chronic pain. For one, it’s focused on the nervous system and brain pathways that generate chronic pain. It’s also developed rapid testing procedures for candidate compounds, a large complex of clinical and data centers, collaborative programs to bring teams together, sustained support for hopeful compounds, and is producing definitive clinical trials.
- Progress appears to be slowly being made. Since 2018 the HEAL Initiative has spent over $2 billion and identified 20 compounds it wants to bring into clinical trials and 3 that are in clinical trials.
- Congress’s substantial increase in HEAL and chronic pain funding this year should provide further momentum.
- The NIH isn’t good at creating programs like HEAL but it does seem good at carrying them out. The HEAL program seems well-organized and conceived and should up speed the time needed to produce better and safer pain drugs.
- It’s one of four large programs (RECOVER Long COVID, Exercise Study, SPARC electroceutical initiative) underway at the NIH which could and should provide insights that FM, ME/CFS and allied disorders should benefit from.
“We know that billions of dollars have been spent on the quest for new pain treatments, and we desperately need safe and effective non-opioid strategies. Historically, the success rate has been very low. Few potential pain drugs make it to clinical testing, and even fewer gain FDA approval. HEAL is making progress toward development of novel medications, devices, and complementary/integrative approaches – and we are eager to sustain this momentum.”
Think to yourself how many different types of pain, for instance, you experience. (Check out “In Their Own Words: Chronic Fatigue Syndrome and Fibromyalgia Patients Describe Their Symptoms” to see the many different types of pain people with these conditions experience.)
The two leaders of the HEAL Initiative’s Preclinical and Translational Research in Pain Management branch, Dr. Christine Colvis, and Dr. Michael Oshinsky, stated that doctors and pain researchers have simply been barking up the wrong tree. As they hammered away at trying to fix the pain in a person’s back or knee, etc. they missed the fact that chronic pain is largely generated in the brain and nerves.
HEAL’s main emphasis is finding targets in the brain and nerves and developing treatments that turn down the pathologically overactivated pain responses seen in chronic pain states. That’s very good news for fibromyalgia (FM), chronic fatigue syndrome (ME/CFS), and the mess of comorbid pain disorders they’re associated with (irritable bowel syndrome, migraine, interstitial cystitis, endometriosis, chronic regional pain syndrome, and others).
I would be shocked if HEAL was funding more than a handful of FM studies, but it’s nerve and brain-based diseases like FM (which has been called the quintessential chronic pain disorder) that will likely benefit the most from this type of focus.
Urgency Recognized
HEAL appears to be quite cognizant of the urgent need to develop new treatments and is determined to find ways to dramatically reduce the time typically needed for developing new drugs and bringing them to market. Noting the 30 years it took to bring the quite successful anti-CGRP migraine drugs to market, Colvis and Oshinsky stated that “that’s a lifetime someone in pain does not have”.
To that end, HEAL has created several novel efforts to speed things up. Its team-based research framework allows HEAL investigators to quickly assess new targets and drugs, dropping the ones that don’t work, and moving on to clinical trials in the ones that do.
HEALS $50 million “Early Phase Pain Investigation Clinical Network” or EPPIC-Net (they’re good at producing acronyms :)), is a network of clinical and data coordinating centers that can be used to rapidly assess new pain drugs. EPPIC-NeT has developed a rapid three-step screening process to determine which treatments to test.
EPPIC-NeT’s focus on producing bulletproof trials will hopefully put another question that haunts Mark Wallace, M.D., of the University of California, San Diego to rest. Wallace wonders whether good pain drugs are, in fact, already out there but failed because their clinical trials were too small or were poorly conceived. EPPIC-NeT is ensuring that its trials will be robust and rigorous enough to provide data one can count on. To that end, HEAL’s completion of a “common data elements” program means all its efforts will be able to “talk” to and inform each other.
All in all, like the NIH’s RECOVER long-COVID program, its HEAL program for chronic pain seems well-conceived and thought out. The NIH may not be good at creating these programs – it seems to need Congress to do that – but once it has them, it appears to carry them out in a thoughtful and well-organized manner.
Is HEAL Healing Yet?
So where are we four years and $2 billion dollars later? HEAL has not brought any drugs to the market yet. At a recent meeting, though, Rebecca Baker, the director of HEAL initiative, reported that HEAL has funded 600 research projects which have resulted in 20 investigational new drug applications (INDs) to the FDA. INDs are actually a big step forward, as they allow a company to start testing its drug in human trials.
These applications include new drugs and repurposed drugs not currently used to treat pain but which HEAL’s studies suggest could be helpful. As of 2021, three trials of novel pain drugs had been funded. Baker stated that the HEAL initiative is currently “testing multiple different treatments for both pain and addiction.”
Thus far, the NIH has awarded $32.3 million to support the development of non-addictive small molecules and biologic agents that may be able to help with chronic pain. They include a very wide variety of factors, including cannabinoid receptor agonists designed to pump up the cannabinoid “feel good” system which some believe is underactive in FM. (I find that high THC gummies not only help me sleep but also help me “exercise” better without pain.) Others include “stem-cell loaded microgels”, Nav1.7 ion channel blockers, bacterial therapies for the gut microbiome, etc.
This is surely just the beginning, though. At the end of last year, NINDS Director Walter Koroshetz, acknowledging that “we have largely failed in effectively removing suffering due to chronic pain conditions“, reported that the projected 2022 Congressional budget will dramatically increase funding for chronic pain and increase funding for the HEAL initiative.
Subsequently, the NIH reported that it expects to spend about $100 million more on chronic pain ($852 million) and almost $400 million more on opioid addiction ($1.2 billion) than it did last year. That new Congressional funding has prompted the NIH to publish a variety of new funding opportunities. Some of the funding suggests the NIH believes it’s time to step up to more trials. Some of the awards include:
- studies to narrow in on new targets in the peripheral nervous system, central nervous system, immune system, or other tissues that can be used to tamp pain levels down
- funding to support multidisciplinary teams in getting small biologic drugs to the place where larger trials can be done
- two-year (beginner’s) awards designed to establish teams and help them take their ideas and participation to the next level
- awards to help move promising biologic or small molecule drugs to the point where an investigational new drug (IND) application can be filed with the FDA and clinical trials can begin
- studies to facilitate the discovery of biomarkers or biosignatures of pain that can be used to test the effectiveness of pain drugs. Moving from the subjectivity of symptom questionnaires to actual biological measurements of pain is a huge need.
Conclusion
Four years in the NIH’s HEAL initiative has not healed chronic pain yet – but no one really expected it to this quickly. Producing an effective and safe drug to treat chronic pain, is, after all, one of the most challenging tasks drug companies face. In spite of the tremendous payday accruing to any company able to do that, many companies had given up.
How good it was then that Congress gave the world of pain research a big boost with a project that combines the basic science needed to find good targets for pain drugs with a fast-track system to identify and test drugs. HEAL’s focus on understanding how nerve-brain pathologies contribute to chronic pain would appear to put FM, ME/CFS, and other chronic pain diseases in the sweet spot to benefit from HEALs findings. Thus far, HEAL has produced 20 drugs seeking to undergo clinical trials and 3 drugs in clinical trials.
Understanding the very complex pain production system takes time, but with HEAL taking a strategic approach – focusing on basic science, fostering collaboration, producing effective studies, supporting early efforts to develop pain drugs, and then helping them through the complex regulatory mechanism – hopefully, less time than one might think.
HEAL is one of four major NIH initiatives that FM, ME/CFS, and like diseases could and should benefit from. It, the NIH’s $1.15 billion RECOVER Long COVID Initiative, the $170 million exercise study, and the SPARC electroceutical initiative should, over time, help us better understand and ultimately treat these diseases.
Where else would you find out about these large-scale efforts underway?
Had never even heard of this, and now it is such an obvious topic. Thanks!
I live in chronic pain, and it seems to be increasing lately as I age, and I’ve acquired more problems (along with the ME/CFS) that HURT.
I have an appointment in three days to discuss pain management with my GP, and am already worrying about it: they don’t want you taking opioids – and have nothing else to offer that will actually make your pain better.
And the opioids cause such profound brain fog I won’t take them. I’m a novelist now that I’ve lost my physics, and I NEED to write, and I’m deathly slow already.
Hope they find something with my tax money. I needed it yesterday.
Not good.
I’m sorry to hear you have chronic pain conditions. I had chronic pain from Lyme and then ME/CFS until I was lucky enough to get into remission by a lot of trial and error plus a really good acupuncturist and suggestions from Cort on this website. My number one pain reliever was CBD with some THC at times. I was never pain free but it was tolerable, I never used aspirin, Tylenol or Ibuprofen (or opioids!) because I wanted my liver and kidneys as healthy as possible to detox all the herbs and supplements I was on. I highly recommend CBD tinctures until you learn the type and dosage you need and talking to a cannabis specialist for help choosing the variety best for you. If you haven’t used CBD I suggest you try it, There are no side effects when dosed correctly for pain (I survived meningitis on CBD/THC alone) and it could change your life for the better. Blessings.
The FDA approved product is right in front of you. It is called Actipatch sold by Bioelectronics in Fredick, MD. Proven. effective and not ingested. Approved around the world and the product really works.
Skin biopsies performed by Kosmidis’s group found that 41% of ME/CFS patients had small fiber Neuropathy (J. Neuro Sci; Dec -2014). Martinez-Lavin’s lab showed that glutamate produced in the dorsal horn ganglia of the spinal cord, was elevated in ME/CFS patients. Sprouting of dorsal root ganglia tissue causes excessive firing of the sympathetic nervous system, and inhibits parasympathetic nervous system control over the sympathetic. Sprouting could be due to a physical injury, inflammation, or infection. The Vagus nerve is the master of the parasympathetic. Some Neurologists believe ME/CFS patients have a viral infection in the Vagus. (Martinez-Lavin, Clinical Rheumatology; Oct. 2021). I am confident that we are not going to get this line of detailed thought from the NIH tortoises.
To address chronic pain they’re clearly going to need to go outside the box and eliminate the “addiction” to drug companies. The history of opioids is actually thousands of years old, dating back to Mesopotamia, 3,400 BC. Heck, Hong Kong was ceded to the British by the Chinese due to the wars over opioid addiction in the 1700’s. It’s estimated that 90% of US heroin addicts started out on opioids. As mentioned, most people that study chronic pain think the solution lies in the brain, not in the perceived “source” of the pain, eg. back, neck, etc.,. There will need to be new insights to solve this one!
They’re definitely done with opioids and tweaking those pathways. Expect very, very different options to show up.
I can give you an option right now. ME/CFS suffer here. After Dr.Phair’s work, I cut out 90% of my carbohydrate consumption. The excruciating pain in my legs disappeared almost immediately. And it has continued to stay away. Think about it. Nearly Everyone in America abuses carbohydrates. They will eventually find that 80+ percent of chronic pain is related to the tryptophan or similar pathway(s) related to dysfunctional carbohydrate metabolism.
This is hopeful for the future. One way I describe my pain is “it’s a thousand layers of pain, overlapping, unrelenting, 24/7. Many things help with the pain, so even though we have positive response at times, removing one layer….leaves 999 more layers to remove.”
That is a very out dated “NIH attitude” toward pain. Small fiber neuropathy upon biopsy in the periphery does not fit into NIH’s hope this is a “perceived pain”. Low Dose Naltrexone reduces microglial inflammation as seen on PET scans, and eventually reduces pain. The NIH is “late to the game”. They look foolish, and will continue to hope this is a “perceived pain” problem.
As I read this I kept wondering about the test subjects who will be used. So often clinical trials do not include women. I hope they will look at the fact that women might need a completely different pain approach from men, and will tackle that.
If they’re serious and they certainly seem to be they will have to address that as women are hit harder by chronic pain than men.
We recently did a blog on this – https://www.healthrising.org/blog/2022/04/02/gender-gap-pain-fibromyaliga-women/ – its fascinating!
Has anyone researched calcitonin, the thyroid-produced hormone that helps with bone integrity? It is said to be 40-60 times more powerful than morphine for pain relief, according to C. Norman Shealy, M.D., Ph.D. He first studied acupuncture in the 1960’s to use in his pain clinic and has since developed a simple 30-second acupressure routine. If daytime body temp. is below 98.6, address thyroid first before using. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524232/
Your answer was purchased from NASA years ago by Andrew Whelan.
Bioelectronics, Frederick, MD. has the patented product named Actipatch, Restorex. No opoids, no chemicals. Sold in retail called KT Tape Wave in Walgreens, Amazon and others.