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Phase 3 Completed N=614 Randomized Quadruple-blind Treatment

A Study Evaluating The Efficacy And Safety Of CP-690,550 In Patients With Moderate To Severe Ulcerative Colitis

Source: ClinicalTrials.gov NCT01465763 ↗
Enrolled (actual)
614
Serious AEs
3.4%
Results posted
Jun 2016
Primary outcomePrimary: Percentage of Participants With Remission at Week 8 — 18.5; 8.2 percentage of participants — p=0.0070
◆ Published Evidence
Highly cited
120citations · ~40 / year
Identification of two tofacitinib subpopulations with different relative risk versus TNF inhibitors: an analysis of the open label, randomised controlled study ORAL Surveillance.
Annals of the rheumatic diseases · 2023 · Open access · Likely link

Summary

This study is designed to evaluate the efficacy and safety of tofacitinib (CP-690,550) in patients with moderate to severe ulcerative colitis who have failed or be intolerant to one of following treatments for ulcerative colitis: oral steroids, azathiopurine/6-mercaptopurine, or anti-TNF-alpha therapy.

Linked Publications (5)

  • Identification of two tofacitinib subpopulations with different relative risk versus TNF inhibitors: an analysis of the open label, randomised controlled study ORAL Surveillance.
    Annals of the rheumatic diseases · 2023 · 120 citations · Open access · Likely link
  • Major Adverse Cardiovascular Events by Baseline Cardiovascular Risk in Patients with Ulcerative Colitis Treated with Tofacitinib: Data from the OCTAVE Clinical Programme.
    Journal of Crohn's & colitis · 2023 · 23 citations · Open access · Likely link
  • Association Between Smoking Status and the Efficacy and Safety of Tofacitinib in Patients with Ulcerative Colitis.
    Crohn's & colitis 360 · 2024 · 5 citations · Open access · Likely link
  • Presence of risk factors associated with colectomy among patients with ulcerative colitis: a <i>post hoc</i> analysis of data from the tofacitinib OCTAVE ulcerative colitis clinical program.
    Therapeutic advances in gastroenterology · 2023 · 2 citations · Open access · Likely link
  • Impact of Concomitant Corticosteroids on Tofacitinib Induction Efficacy and Infection Rates in Ulcerative Colitis.
    Digestive diseases and sciences · 2023 · 1 citation · Open access · Likely link

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants With Remission at Week 8
18.5; 8.2 0.0070 sig
SECONDARY
Percentage of Participants Achieving Mucosal Healing at Week 8
31.3; 15.6 0.0005 sig
SECONDARY
Percentage of Participants Achieving Clinical Response at Week 8
59.9; 32.8 <0.0001 sig
SECONDARY
Percentage of Participants With Endoscopic Remission at Week 8
6.7; 1.6 0.0345 sig
SECONDARY
Percentage of Participants With Clinical Remission at Week 8
18.5; 8.2 0.0070 sig
SECONDARY
Percentage of Participants With Symptomatic Remission at Week 8
11.8; 5.7 0.0601
SECONDARY
Percentage of Participants With Deep Remission at Week 8
6.5; 0 0.0043 sig
SECONDARY
Partial Mayo Scores
6.3; 6.5; 4.2; 5.2; 3.5; 4.8
SECONDARY
Change From Baseline in Partial Mayo Scores at Weeks 2, 4 and 8
-2.1; -1.2; -2.8; -1.6; -3.1; -1.6 <0.0001 sig
SECONDARY
Change From Baseline in Total Mayo Scores at Week 8
9.0; 9.1; -3.8; -1.9 <0.0001 sig

Eligibility Criteria

Inclusion Criteria

  • Subject must be at least 18 years of age.
  • Males and females with a documented diagnosis of UC at least 4 months prior to entry into the study.
  • Subjects with moderately to severely active UC based on Mayo score criteria.
  • Subjects must have failed or be intolerant of at least one of the following treatments for UC:
  • Corticosteroids (oral or intravenous).
  • Azathioprine or 6 mercaptopurine (6 MP).
  • Anti TNF-alpha therapy.

Exclusion Criteria

  • Presence of indeterminate colitis, microscopic colitis, ischemic colitis, infectious colitis, or clinical findings suggestive of Crohn's disease.
  • Subjects with disease limited to distal 15 cm.
  • Subjects without previous treatment for UC (ie, treatment naïve).
  • Subjects displaying clinical signs of fulminant colitis or toxic megacolon.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01465763) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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