News|Articles|March 27, 2024

Designing Clinical Studies in Pain Management

In part 2 of this video interview, Greg Sturmer, co-founder and CEO of Elysium Therapeutics discusses what industry should be keeping top of mind when it comes to designing and executing pain clinical studies.

ACT: What should industry be keeping top of mind when it comes to designing and executing pain clinical trials?

Greg Sturmer: I guess the first part is kind of, regardless of whether it's pain, or another indication is what's always of utmost importance is to keep the end in mind. And the end in this case is, what do I want in my product label? What's going to be in that label? Because the information that's in the label is what the company is going to be able to use to market that product. So, what the focus should be on is: how are we going to differentiate our product from what else is out there? So, I mean, the Nirvana is: I'm going to improve on safety, and have a very specific set of clinical studies that support that I've got a product that's much safer than what's out on the market. And/or I suppose, efficacy, I can set myself apart from the competition, because I've got a more effective medication. So I think designing your studies from a safety perspective that says, “Here is the data that shows that we're better than the current product that leads in the market space as it applies to us.” That's why our focus is on what we call SMART products. That acronym stands for safer medicines that alleviate risks and trauma. And our effort is to create smart medicines, in pain, smart medicines for opioid use disorder, and smart rescue agents. When it comes to efficacy when you're trying to differentiate a product from the market, let's bring it to the pain space. There's been a concerted effort over the decades to develop a non-opioid pain reliever that's as or more effective than opioids. And that's a high bar, because opioids have unmatched efficacy and are unmatched across a spectrum of causes of pain. So, I would say the important thing to do when designing your clinical study is to go head-to-head with whatever is the standard of care. And in the case of pain, opioids, and demonstrate how are you better.


Related to this article

What the Epilepsy Community Has Taught Us About Trial Feasibility
In this video interview, Amélie Lothe, global medical community head for rare epilepsies at UCB Pharma, shares what she has learned firsthand from families living with Dravet syndrome and CDKL5 deficiency disorder about what makes trial participation possible—and what makes it not.
Why Seizure Counts Alone Can't Define Success in Epilepsy Trials
In this video interview, Amélie Lothe, global medical community head for rare epilepsies at UCB Pharma, explains why the full burden of developmental and epileptic encephalopathies extends far beyond clinical symptoms—and why endpoints must reflect what families are actually hoping for.
What It Actually Means to Embed the Patient Voice in Trial Design
In this video interview, Amélie Lothe, global medical community head for rare epilepsies at UCB Pharma, explains why genuine patient partnership begins before the protocol is written—and what it looks like when patients and caregivers tell you a trial was designed with them in mind.
What This Study Means for Sponsors Still Struggling to Justify RBQM at Scale
In this video interview, Sylviane de Viron of CluePoints and Abigail Dirks of Tufts CSDD explain how ICH E6(R3) and new empirical evidence of RBQM's net financial impact give sponsors the tools they need to build the multi-functional buy-in required for successful adoption—and why RBQM only delivers full value when it replaces, not supplements, traditional monitoring.