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27 Nov 2017
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Risankizumab trumps ustekinumab, placebo in reducing chronic plaque psoriasis severity

Roshini Claire Anthony
03 Oct 2018

Two phase III studies have demonstrated the superiority of the selective interleukin-23p19 inhibitor risankizumab over ustekinumab or placebo in helping patients with moderate-to-severe chronic plaque psoriasis reduce the severity of their condition.

“[S]elective blockade of the p19 subunit of interleukin-23 with risankizumab was superior to dual inhibition of interleukin-12 and interleukin-23 by ustekinumab in providing substantial skin clearance with a rapid onset and durable maintenance, supporting the strategy of a more targeted approach,” said the researchers.

“[T]he absence of fluctuations in efficacy between dosing in risankizumab-treated patients confirms the appropriateness of the 12-week dosing interval,” they added.

Participants in the UltIMMa*-1 (n=506, mean age 48 years, 71 percent male) and UltIMMa-2 (n=491, mean age 47 years, 68 percent male) studies were adults with moderate-to-severe chronic plaque psoriasis enrolled from 139 sites in 14 countries who were randomized to receive either risankizumab (150 mg; n=304 and 294 in UltIMMa-1 and 2, respectively), ustekinumab (45 or 90 mg [weight dependent]; n=100 and 99 in UltIMMa-1 and 2, respectively), or placebo (n=102 and 98 in UltIMMa-1 and 2, respectively).

The studies were divided into parts A (initial 16-week period) and B (weeks 16–52) and study drugs were administered subcutaneously at weeks 0, 4, 16, 28, and 40. Patients who initially received placebo were switched to risankizumab at 16 weeks, with the other patients continuing their initially assigned treatments for up to 52 weeks.

PASI-90** at 16 weeks was achieved by more patients on risankizumab compared with those on placebo (75.3 percent vs 4.9 percent, adjusted difference, 70.3 percent) or ustekinumab (42.0 percent, adjusted difference, 33.5 percent; p<0.0001 for both comparisons) in UltIMMa-1, with similar results observed in UltIMMa-2 (74.8 percent of patients on risankizumab vs 2.0 percent on placebo [adjusted difference, 72.5 percent] and 47.5 percent on ustekinumab [adjusted difference, 27.6 percent; p<0.0001 for both comparisons]). [Lancet 2018;392:650-661]

More patients on risankizumab also achieved sPGA*** score of 0 or 1 at 16 weeks compared with those on placebo (87.8 percent vs 7.8 percent, adjusted difference, 79.9 percent) or ustekinumab (63.0 percent, adjusted difference, 25.1 percent; p<0.0001 for both comparisons) in UltIMMa-1 and in UltIMMa-2 (83.7 percent vs 5.1 percent [placebo], adjusted difference, 78.5 percent, and 61.6 percent [ustekinumab], adjusted difference, 22.3 percent; p<0.0001 for both comparisons).

At week 52, PASI 100 was achieved by more patients randomized to receive risankizumab compared with those who received ustekinumab in both UltIMMa-1 (56.3 percent vs 21.0 percent) and UltIMMa-2 (59.5 percent vs 30.3 percent; p<0.0001 for both studies), as was sPGA 0 (57.6 percent vs 21.0 percent in UltIMMa-1 and 59.5 percent vs 30.3 percent in UltIMMa-2; p<0.0001 for both studies).

By week 52, patients initially on placebo who were switched to risankizumab at week 16 had comparable PASI and sPGA response to those who received risankizumab from study onset.

Treatment-related adverse events (TRAEs) occurred at a similar rate between patients on risankizumab, placebo, and ustekinumab in part A of UltIMMa-1 (49.7, 51.0, and 50.0 percent, respectively) and UltIMMa-2 (45.6, 45.9, and 53.5 percent, respectively) and in patients treated with risankizumab and ustekinumab in part B of UltIMMa-1 (61.3 and 66.7 percent, respectively) and UltIMMa-2 (55.7 and 74.5 percent, respectively). Among patients who switched from placebo to risankizumab, TRAEs occurred in 67.0 and 64.9 percent in UltIMMa-1 and UltIMMa-2, respectively.

“Although our repertoire of psoriasis treatments has rapidly advanced in the past 20 years, risankizumab shows particular promise,” said Drs Abigail Cline and Steven R Feldman from the Wake Forest School of Medicine, Winston-Salem, North Carolina, US, in a commentary. [Lancet 2018;392:616-617]

“Risankizumab had greater efficacy and similar safety compared with placebo and ustekinumab [and] clinical response to risankizumab treatment was rapid,” they said.

The researchers recommended further study to assess long-term outcomes of risankizumab treatment as well as studies involving patients from different ethnic backgrounds to improve the generalizability of the findings.

 

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Most Read Articles
27 Nov 2017
The amino sulphonic acid taurine may safely and effectively reduce portal pressure in cirrhotic patients, a study has shown.
Prof. Vincent Wong, Prof. Ray Kim, Dr. Tan Poh Seng, 10 Sep 2019
Chronic hepatitis B (CHB) remains a major public health concern because of its worldwide distribution and potential adverse sequelae, including cirrhosis and hepatocellular carcinoma (HCC). At a recent symposium held during the GIHep Singapore 2019, Professor Vincent Wong from the Chinese University of Hong Kong and Professor Ray Kim from the Stanford University School of Medicine, Stanford, California, US, discussed antiviral treatments for CHB, with a focus on the novel agent tenofovir alafenamide (Vemlidy®). Dr Tan Poh Seng from the National University Hospital, Singapore, chaired the symposium.
26 Nov 2019
Podcast: Professor R. Scott Wright speaks about the potential role of inclisiran in providing durable reductions in LDL-cholesterol levels in patients with atherosclerotic cardiovascular disease.
Jairia Dela Cruz, 12 Dec 2019
Use of isatuximab (Isa) in combination with pomalidomide and dexamethasone (PomDex) appears to lead to more favourable outcomes in elderly patients with relapsed/refractory multiple myeloma (RRMM) as compared with PomDex alone, according to the results of a subgroup analysis of the ICARIA-MM trial presented at the 61st Annual Meeting of the American Society of Hematology (ASH 2019).