IL-23 inhibitors use is increasing—here's why they have a competitive advantage
Key Takeaways
Industry Buzz
“IL-23s will be most useful in patients who have a large amount of psoriatic skin involvement. They are much better at clearing the skin vs TNF inhibitors.” — Stella Bard, MD, rheumatologist at Arthritis & Rheumatology Care PC Brooklyn
“IL-23 inhibitors are a great option for patients who have concomitant inflammatory bowel disease, since IL-17 inhibitors are contraindicated in this disease population.” — Amy Kehl, MD, a board-certified rheumatologist at Providence Saint John’s Health Center in Santa Monica, CA
Find more of your peers' perspectives and insights below.
Patients with psoriatic arthritis (PsA) often live with debilitating chronic symptoms, ranging from joint and bone pain to skin lesions. Fortunately, physicians have plenty of treatment options for patients with PsA, including a laundry list of effective biologics.
Sales for newer agents, such as the more-recently approved IL-23 inhibitors, are currently skyrocketing.[] And for good reason: IL-23 inhibitors show greater clinical efficacy than other agents, such as IL-12 and TNF inhibitors.
More so, research published in The Lancet found that IL-23 inhibitors resulted in fewer serious adverse events, including infections, when compared to TNF inhibitors.[] Additionally, a recent study showed that psoriasis patients treated with IL-23s were at lower risk of developing PsA than those receiving IL-17 and TNF inhibitors.[]
Related: The truth about the most common misconception about biologics for PsABenefits of treating with IL-23s, per the experts
Stella Bard, MD, a rheumatologist at Arthritis & Rheumatology Care PC in Brooklyn, says that, for starters, IL-23s carry a lower risk of infection than first-generation biologics. But they’re also more effective: “IL-23s will be most useful in patients who have a large amount of psoriatic skin involvement. They are much better at clearing the skin vs TNF inhibitors,” she says. “They should also work longer term, because they have less of a risk of inducing neutralizing antibodies, which are produced by the body, surround the drug, and render it inactive.”
Dr. Bard says patients also prefer the less-frequent administration schedule of IL-23s. For example, risankizumab (Skyrizi) requires one injection four times per year after just two starter doses, vs adalimumab (Humira), which generally requires an injection every other week.[][]
This convenience, Dr. Bard says, “allows for better patient adherence than drugs that require more frequent administration. She adds that IL-23s can also be a “great alternative for people who cannot take a TNF inhibitor."
Positive impacts on IBD symptoms
IL-23s offer gastrointestinal health benefits, too. According to Amy Kehl, MD, a rheumatologist at Providence Saint John’s Health Center in Santa Monica, CA, “IL-23 inhibitors are a great option for patients who have concomitant inflammatory bowel disease, since IL-17 inhibitors are contraindicated in this disease population.”
According to 2024 research published in Expert Opinion on Biological Therapy, the “pivotal role of [IL-23] in the pathogenesis of PsA has become increasingly evident,” making it a topline therapy for PsA.[]
That said, the authors note that more information is needed on the long-term effects of drugs within the IL-23 family, and that drug targets within the IL-23/IL-23 R axis warrant further exploration.
Read Next: 34% of rheumatologists weren’t aware of this key IL-23 inhibitor fact. Are you?