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Clinical Trials/NCT01620255
NCT01620255
Completed
Phase 2

A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)

Shire189 sites in 1 country357 target enrollmentNovember 2, 2012

Overview

Phase
Phase 2
Intervention
Placebo
Conditions
Ulcerative Colitis
Sponsor
Shire
Enrollment
357
Locations
189
Primary Endpoint
Percentage of Participants in Clinical Remission at Week 12
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

To determine the dose or doses of PF-00547659 that will be the most effective to improve or halt the disease symptoms in patients with moderate to severe ulcerative colitis.

Registry
clinicaltrials.gov
Start Date
November 2, 2012
End Date
February 4, 2016
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Shire
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects with diagnosis of Ulcerative Colitis for 3 or more months.
  • Ulcerative colitis must be active beyond the rectum.
  • Must active Ulcerative Colitis with a Total Mayo Score of 6 to 12 points

Exclusion Criteria

  • Pregnant or breast feeding.
  • Diagnosis of indeterminate colitis or Crohn's Disease
  • Subjects with history of colonic or small bowel obstruction or resection.

Arms & Interventions

Placebo

Intervention: Placebo

Drug Dose Level 1

Intervention: PF-00547659 SC Injection

Drug Dose Level 2

Intervention: PF-00547659 SC Injection

Drug Dose Level 3

Intervention: PF-00547659 SC Injection

Drug Dose Level 4

Intervention: PF-00547659 SC Injection

Outcomes

Primary Outcomes

Percentage of Participants in Clinical Remission at Week 12

Time Frame: Week 12

Clinical remission was defined as a Total Mayo Score of less than or equal (\<=) 2 points with no individual subscore exceeding 1 point and rectal bleed subscore of 0 or 1. The Mayo Score is a tool designed to measure disease activity for ulcerative colitis (UC). Scoring ranges from 0 to 12 points and consists of 4 subscores, each graded 0 to 3 with higher score indicating more severe disease activity. Endoscopic readings from the local and the central reader were considered for analysis. The central reading was used as the primary analysis and the local readings were used for the sensitivity analyses.

Secondary Outcomes

  • Percentage of Participants With Mucosal Healing at Week 12(Week 12)
  • Change From Baseline in Inflammatory Bowel Disease Questionnaire (IBDQ) Domain Scores at Week 12(Baseline (BL), Week 12)
  • Percentage of Participants With Change From Baseline in Individual Mayo Subscore - Findings on Flexible Sigmoidoscopy - at Week 12(Baseline, Week 12)
  • Percentage of Participants With Clinical Response at Week 12(Week 12)
  • Change From Baseline in Total Mayo Score at Week 12(Baseline, Week 12)
  • Percent Change From Baseline in High Sensitivity C-reactive Protein (hsCRP) at Weeks 4, 8, and 12(Baseline; Weeks 4, 8, and 12)
  • Change From Baseline in Inflammatory Bowel Disease Questionnaire (IBDQ) Total Score at Week 12(Baseline, Week 12)
  • Maximum Serum PF-00547659 Concentration Achieved(Weeks 0 (baseline), 2, 4,8, 12, 16, 20, 24, 28, 32, and 36; Early Withdrawal)
  • Percentage of Participants With Absolute Partial Mayo Score of Less Than or Equal to (<=) 2 With no Individual Subscore More Than (>) 1 at Weeks 4, 8, and 12(Weeks 4, 8, and 12)
  • Percentage of Participants With Change From Baseline in Individual Mayo Subscores - Stool Frequency, Rectal Bleeding, and Physician's Global Assessment (PGA) - at Weeks 4, 8, and 12(Baseline; Weeks (W) 4, 8, and 12)
  • Percent Change From Baseline in Fecal Calprotectin at Weeks 4, 8, and 12(Baseline, Weeks 4, 8, and 12)
  • Percentage of Participants With an Inflammatory Bowel Disease Questionnaire (IBDQ) Total Score of More Than or Equal to (>=) 170 at Week 12(Week 12)
  • Number of Participants With Treatment-emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs), and Withdrawals Due to TEAEs During the Treatment Period (Weeks 0-12)(Screening through to end of treatment period, up to 12 weeks)

Study Sites (189)

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