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A phase 2 study of Tofacitinib, an oral janus kinase inhibitor, inpatients with crohn's disease

  • William J. Sandborn
  • , Subrata Ghosh
  • , Julian Panes
  • , Ivana Vranic
  • , Wenjin Wang
  • , Wojciech Niezychowski

Research output: Contribution to journalArticlepeer-review

Abstract

Background & Aims: Tofacitinib, an orally administered Janus kinase inhibitor, blocks signaling through γ-chain-containing cytokines (interleukins 2, 4, 7, 9, 15, and 21). We performed a phase 2 trial to measure its efficacy in patients with moderate-to-severe active Crohn's disease. Methods: Patients (N= 139; age, ≥18 y) with moderate-to-severe active Crohn's disease were assigned randomly to groups given 1 mg (n= 36), 5 mg (n= 34), or 15 mg (n= 35) tofacitinib or placebo (n= 34), twice daily for 4 weeks, at 48 centers in 12 countries. The primary end point was the proportion of clinical responders at week 4 (decrease from baseline in the Crohn's Disease Activity Index score of ≥70 points [Response-70]). Secondary end points included clinical remission (Crohn's Disease Activity Index score of <150 points) at week4. Results: A clinical response was observed in 36% (P=.467), 58% (P=.466), and 46% (P ≥.999) of patients given the 1-, 5-, and 15-mg doses of tofacitinib, compared with 47% of patients given placebo. Clinical remission was observed in 31% (P=.417), 24% (P=.776), and 14% (P=.540) of patients given the 1-, 5-, and 15-mg doses of tofacitinib, compared with 21% of patients given placebo. The 15-mg dose of tofacitinib reduced levels of C-reactive protein and fecal calprotectin from baseline. Adverse and serious adverse events were similar among groups. Dose-dependent increases in low- and high-density lipoprotein cholesterol were observed in patients given the 5- or 15-mg doses of tofacitinib. Conclusions: There were no significant differences in the percentage of patients with moderate-to-severe active Crohn's disease who achieved clinical responses (Response-70) or clinical remission after 4 weeks' administration of tofacitinib (1, 5, or 15 mg) or placebo twice daily. However, a large percentage of patients given placebo achieved Response-70 or remission. Reductions in C-reactive protein and fecal calprotectin levels among patients given the 15-mg dose of tofacitinib indicate its biologic activity.

Original languageEnglish
Pages (from-to)1485-1493.e2
JournalClinical Gastroenterology and Hepatology
Volume12
Issue number9
DOIs
Publication statusPublished - Sep 2014
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • CP-690,550
  • Crohn's disease
  • Randomized control trial
  • Tofacitinib

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