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A Study of the Efficacy and Safety of Etrolizumab in Ulcerative Colitis Participants Who Are Refractory to or Intolerant of Tumor Necrosis Factor (TNF) Inhibitors

This study is currently recruiting participants.
Verified June 2017 by Hoffmann-La Roche
Sponsor:
ClinicalTrials.gov Identifier:
NCT02100696
First Posted: April 1, 2014
Last Update Posted: July 2, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Information provided by (Responsible Party):
Hoffmann-La Roche
  Purpose
This phase III, double blind, placebo-controlled, multicenter study will investigate the efficacy and safety of etrolizumab during induction and maintenance of remission in participants with moderately to severely active ulcerative colitis (UC) who are refractory to or intolerant of TNF inhibitors.

Condition Intervention Phase
Ulcerative Colitis Drug: Etrozulimab Drug: Placebo Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: Phase III, Double Blind, Placebo-Controlled, Multicenter Study of the Efficacy and Safety of Etrolizumab During Induction and Maintenance in Patients With Moderate to Severe Active Ulcerative Colitis Who Are Refractory to or Intolerant of TNF Inhibitors

Resource links provided by NLM:


Further study details as provided by Hoffmann-La Roche:

Primary Outcome Measures:
  • Percentage of Participants With Remission as Determined by the Mayo Clinic Score (MCS) [ Time Frame: Week 14 ]
  • Percentage of Participants With Remission at Week 66 Among Randomized Participants in Clinical Remission at Week 14, as Determined by the MCS [ Time Frame: Week 66 ]

Secondary Outcome Measures:
  • Percentage of Participants With Clinical Remission at Week 14 (Induction Phase) and Week 66 (Maintenance Phase), as Determined by MCS [ Time Frame: Week 14, 66 ]
  • Percentage of Participants With Clinical Response at Week 14 (Induction Phase) and Week 66 (Maintenance Phase) [ Time Frame: Week 14, 66 ]
  • Percentage of Participants With Improvement From Baseline in Endoscopic Appearance of the Mucosa at Week 14 (Induction Phase) and Week 66 (Maintenance Phase) [ Time Frame: Week 14, 66 ]
  • Percentage of Participants With Endoscopic Remission at Week 14 (Induction Phase) and Week 66 (Maintenance Phase) [ Time Frame: Week 14, 66 ]
  • Change From Baseline to Week 14 and Week 66 in UC Bowel Movement Signs and Symptoms, as assessed by Ulcerative Colitis Patient-Reported Bowel Movement Signs and Symptoms (UC-PRO/SS) [ Time Frame: Baseline, Week 14, 66 ]
  • Change From Baseline to Week 14 and Week 66 in UC Abdominal Symptoms, as assessed by UC-PRO/SS [ Time Frame: Baseline, Week 14, 66 ]
  • Change From Baseline to Week 14 and Week 66 in Health Related Quality of Life (QoL), as assessed by the Overall Score of Inflammatory Bowel Disease Questionnaire (IBDQ) [ Time Frame: Baseline, Week 14, 66 ]
  • Percentage of Participants With Corticosteroid-Free Clinical Remission at Week 66 Among Participants who Were Receiving Corticosteroids at Baseline [ Time Frame: Week 66 ]
  • Percentage of Participants With Corticosteroid-Free Remission at Week 66 Among Participants who Were Receiving Corticosteroids at Baseline [ Time Frame: Week 66 ]
  • Area Under the Serum Concentration-Time Curve (AUC) [ Time Frame: pre-dose (0 hours), post-dose on Week 14, 24, 44, 66 ]
  • Maximum Observed Serum Concentration (Cmax) [ Time Frame: pre-dose (0 hours), post-dose on Week 14, 24, 44, 66 ]
  • Minimum Observed Serum Trough Concentration at Steady State (Ctrough,ss) [ Time Frame: pre-dose on Week 14, 24, 44, 66 ]
  • Percentage of Participants With Anti-therapeutic Antibodies to Etrolizumab [ Time Frame: Baseline up to Week 66 ]

Estimated Enrollment: 800
Actual Study Start Date: May 31, 2014
Estimated Study Completion Date: January 9, 2019
Estimated Primary Completion Date: January 9, 2019 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Cohort 1: Etrolizumab (Open-label Induction Phase)
All participants will receive treatment with open-label etrolizumab 105 milligram (mg) subcutaneous injection every 4 weeks for 14 weeks.
Drug: Etrozulimab
Participants will receive 105 mg administered by subcutaneous injection every 4 weeks.
Other Name: PRO145223, RO549026
Experimental: Cohort 2: Etrolizumab (Double-blind Induction Phase)
All participants will receive treatment with etrolizumab 105 mg subcutaneous injection every 4 weeks for 14 weeks.
Drug: Etrozulimab
Participants will receive 105 mg administered by subcutaneous injection every 4 weeks.
Other Name: PRO145223, RO549026
Placebo Comparator: Cohort 2: Placebo (Double-blind Induction Phase)
All participants will receive treatment with placebo matched with etrolizumab.
Drug: Placebo
Participants will receive placebo matched with etrolizumab.
Experimental: Etrolizumab (Maintenance Phase)
Participants who achieved a clinical response at Week 14 during induction phase (etrolizumab open-label and double blind arm) and randomized to this arm will receive etrolizumab 105 mg subcutaneous injection every 4 weeks up to week 66.
Drug: Etrozulimab
Participants will receive 105 mg administered by subcutaneous injection every 4 weeks.
Other Name: PRO145223, RO549026
Placebo Comparator: Placebo (Maintenance Phase)
Participants who achieved a clinical response at Week 14 during induction phase (etrolizumab open-label and double blind arm, placebo double blind arm) and are randomized to this arm will receive placebo matched to etrolizumab.
Drug: Placebo
Participants will receive placebo matched with etrolizumab.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Moderately to severely active UC as determined by the Mayo Clinic Score assessment (MCS)
  • Intolerance, loss response or failure to respond to treatment with at least one TNF-inhibitor within the previous 5 years
  • Washout of anti-TNF therapy for at least 8 weeks preceding Day 1
  • Background regimen for UC may include oral 5-aminosalicylic acid (5-ASA), oral corticosteroids, budesonide multi-matrix system (MMX), probiotics, azathioprine (AZA), 6-mercaptopurine (6-MP), or methotrexate (MTX) if doses have been stable during the screening period
  • Use of highly effective contraception as defined by the protocol
  • Must have received a colonoscopy within the past year or be willing to undergo a colonoscopy in lieu of a flexible sigmoidoscopy at screening

Exclusion Criteria:

  • A history of or current conditions and diseases affecting the digestive tract, such as indeterminate colitis, Crohn's disease, fistulas or abdominal abscesses, colonic mucosal dysplasia, intestinal obstruction, toxic megacolon, or unremoved adenomatous colonic polyps
  • Prior or planned surgery for UC
  • Past or present ileostomy or colostomy
  • Any prior treatment with etrolizumab or other anti-integrin agents (including natalizumab, vedolizumab, and efalizumab) and rituximab
  • Chronic hepatitis B or C infection, human immunodeficiency virus (HIV) or tuberculosis
  • Evidence of or treatment for Clostridium difficile clinically significant cytomegalovirus (CMV) colitis within 60 days prior to Day 1
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02100696


Contacts
Contact: Reference Study ID Number: GA28950 www.roche.com/about_roche/roche_worldwide.htm 888-662-6728 (U.S. and Canada) global.rochegenentechtrials@roche.com

  Show 348 Study Locations
Sponsors and Collaborators
Hoffmann-La Roche
Investigators
Study Director: Clinical Trials Hoffmann-La Roche
  More Information

Responsible Party: Hoffmann-La Roche
ClinicalTrials.gov Identifier: NCT02100696     History of Changes
Other Study ID Numbers: GA28950
2013-004278-88 ( EudraCT Number )
First Submitted: March 27, 2014
First Posted: April 1, 2014
Last Update Posted: July 2, 2017
Last Verified: June 2017

Additional relevant MeSH terms:
Colitis
Ulcer
Colitis, Ulcerative
Gastroenteritis
Gastrointestinal Diseases
Digestive System Diseases
Colonic Diseases
Intestinal Diseases
Pathologic Processes
Inflammatory Bowel Diseases