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A phase 3 trial of seladelpar in primary biliary cholangitis

Erişim

info:eu-repo/semantics/closedAccess

Tarih

2024

Yazar

Hirschfield, Gideon M.
Bowlus, Christopher L.
Mayo, Marlyn J.
Kremer, Andreas E.
Vierling, John M.
Kowdley, Kris V.
Levy, Cynthia
Villamil, Alejandra
Ladrón de Guevara Cetina, Alma L.
Janczewska, Ewa
Zigmond, Ehud
Jeong, Sook-Hyang
Yılmaz, Yusuf
Kallis, Yiannis
Corpechot, Christophe
Buggisch, Peter
Invernizzi, Pietro
Hurtado, Maria Carlota Londoño
Bergheanu, Sandrin
Yang, Ke
Choi, Yun-Jung
Crittenden, Daria B.
McWherter, Charles A.

Üst veri

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Künye

Hirschfield, G. M., Bowlus, C. L., Mayo, M. J., Kremer, A. E., Vierling, J. M., Kowdley, K. V., Levy, C., Villamil, A., Ladrón de Guevara Cetina, A. L., Janczewska, E., Zigmond, E., Jeong, S. H., Yilmaz, Y., Kallis, Y., Corpechot, C., Buggisch, P., Invernizzi, P., Londoño Hurtado, M. C., Bergheanu, S., Yang, K., … RESPONSE Study Group (2024). A Phase 3 Trial of Seladelpar in Primary Biliary Cholangitis. The New England journal of medicine, 390(9), 783–794. https://doi.org/10.1056/NEJMoa2312100

Özet

Effective treatments for patients with primary biliary cholangitis are limited. Seladelpar, a peroxisome proliferator–activated receptor delta agonist, has potential benefits. METHODS In this phase 3, 12-month, double-blind, placebo-controlled trial, we randomly assigned (in a 2:1 ratio) patients who had had an inadequate response to or who had a history of unacceptable side effects with ursodeoxycholic acid to receive oral seladelpar at a dose of 10 mg daily or placebo. The primary end point was a biochemical response, which was defined as an alkaline phosphatase level less than 1.67 times the upper limit of the normal range, with a decrease of 15% or more from baseline, and a normal total bilirubin level at month 12. Key secondary end points were normalization of the alkaline phosphatase level at month 12 and a change in the score on the pruritus numerical rating scale (range, 0 [no itch] to 10 [worst itch imaginable]) from baseline to month 6 among patients with a baseline score of at least 4 (indicating moderate-to-severe pruritus). RESULTS Of the 193 patients who underwent randomization and treatment, 93.8% received ursodeoxycholic acid as standard-of-care background therapy. A greater percentage of the patients in the seladelpar group than in the placebo group had a biochemical response (61.7% vs. 20.0%; difference, 41.7 percentage points; 95% confidence interval [CI], 27.7 to 53.4, P<0.001). Normalization of the alkaline phosphatase level also occurred in a greater percentage of patients who received seladelpar than of those who received placebo (25.0% vs. 0%; difference, 25.0 percentage points; 95% CI, 18.3 to 33.2, P<0.001). Seladelpar resulted in a greater reduction in the score on the pruritus numerical rating scale than placebo (least-squares mean change from baseline, -3.2 vs. -1.7; least-squares mean difference, -1.5; 95% CI, -2.5 to -0.5, P=0.005). Adverse events were reported in 86.7% of the patients in the seladelpar group and in 84.6% in the placebo group, and serious adverse events in 7.0% and 6.2%, respectively. CONCLUSIONS In this trial involving patients with primary biliary cholangitis, the percentage of patients who had a biochemical response and alkaline phosphatase normalization was significantly greater with seladelpar than with placebo. Seladelpar also significantly reduced pruritus among patients who had moderate-to-severe pruritus at baseline. The incidence and severity of adverse events were similar in the two groups.

Kaynak

New England Journal of Medicine

Cilt

390

Sayı

9

Bağlantı

https://doi.org/10.1056/NEJMoa2312100
https://hdl.handle.net/11436/8882

Koleksiyonlar

  • PubMed İndeksli Yayınlar Koleksiyonu [2443]
  • Scopus İndeksli Yayınlar Koleksiyonu [5931]
  • TF, Dahili Tıp Bilimleri Bölümü Koleksiyonu [1559]
  • WoS İndeksli Yayınlar Koleksiyonu [5260]



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