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A Multicenter, Randomized, Double-Blind, Placebo Controlled Induction Study to Evaluate the Efficacy and Safety of Risankizumab in Subjects With Moderately to Severely Active Ulcerative Colitis Who Have Failed Prior Biologic Therapy

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ClinicalTrials.gov Identifier: NCT03398148
Recruitment Status : Recruiting
First Posted : January 12, 2018
Last Update Posted : December 6, 2019
Sponsor:
Information provided by (Responsible Party):
AbbVie

Tracking Information
First Submitted Date  ICMJE January 8, 2018
First Posted Date  ICMJE January 12, 2018
Last Update Posted Date December 6, 2019
Actual Study Start Date  ICMJE March 7, 2018
Estimated Primary Completion Date September 23, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: January 8, 2018)
Percentage of participants with clinical remission per adapted Mayo Score at Week 12 [ Time Frame: Week 12 ]
Clinical remission per adapted Mayo Score.
Original Primary Outcome Measures  ICMJE Same as current
Change History Complete list of historical versions of study NCT03398148 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures  ICMJE
 (submitted: November 2, 2018)
  • Percentage of participants achieving clinical remission per full Mayo Score at Week 12 in subjects with a full Mayo score of 6 to 12 at Baseline [ Time Frame: Week 12 ]
    Clinical remission per full Mayo Score.
  • Ulcerative Colitis Symptom Questionnaire (UC-SQ): Change from Baseline to Week 12 [ Time Frame: Baseline, Week 12 ]
    The US-SQ is a patient questionnaire to assess severity of Crohn's symptoms.
  • Inflammatory Bowel Disease Questionnaire (IBDQ): Change from Baseline to Week 12 [ Time Frame: Baseline, Week 12 ]
    The IBDQ is used to assess the quality of life of patients with inflammatory bowel disease.
  • Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue): Change from Baseline to Week 12 [ Time Frame: Baseline, Week 12 ]
    The FACIT-Fatigue is a validated tool that measures an individual's level of fatigue during their usual daily activities over the past week.
  • Percentage of participants achieving clinical response per adapted Mayo Score at week 12 [ Time Frame: Week 12 ]
    Clinical response per adapted Mayo Score.
  • Percentage of participants with endoscopic remission at Week 12 [ Time Frame: Week 12 ]
    Endoscopic remission per endoscopy subscore.
  • Percentage of participants achieving clinical response per partial adapted Mayo Score at week 4 [ Time Frame: Week 4 ]
    Clinical response per partial adapted Mayo Score (without endoscopy).
  • Percentage of participants with mucosal healing at Week 12 [ Time Frame: Week 12 ]
    Mucosal healing defined as endoscopic and histologic remission.
  • 36-Item Short Form Health Status Survey (SF-36): Change from Baseline to Week 12 [ Time Frame: Baseline, Week 12 ]
    The SF-36 is an indicator of overall health status.
  • Percentage of participants with hospitalization through Week 12 [ Time Frame: 12 weeks ]
    Participants with an event that results in admission to the hospital.
  • Percentage of participants with Ulcerative Colitis (UC)-related surgeries through Week 12 [ Time Frame: 12 weeks ]
    Participants who underwent surgery related to UC.
  • Percentage of participants with endoscopic improvement at Week 12 [ Time Frame: Week 12 ]
    Endoscopic improvement per endoscopy subscore.
Original Secondary Outcome Measures  ICMJE
 (submitted: January 8, 2018)
  • Percentage of participants with endoscopic improvement at Week 12 [ Time Frame: Week 12 ]
    Endoscopic improvement per endoscopy subscore.
  • Percentage of participants achieving clinical remission per full Mayo Score at Week 12 in subjects with a full Mayo score of 6 to 12 at Baseline [ Time Frame: Week 12 ]
    Clinical remission per full Mayo Score.
  • Percentage of participants achieving clinical response per adapted Mayo Score at week 12 [ Time Frame: Week 12 ]
    Clinical response per adapted Mayo Score.
  • Percentage of participants achieving clinical response per partial adapted Mayo Score at week 4 [ Time Frame: Week 4 ]
    Clinical response per partial adapted Mayo Score (without endoscopy).
  • Percentage of participants with endoscopic remission at Week 12 [ Time Frame: Week 12 ]
    Endoscopic remission per endoscopy subscore.
  • Percentage of participants with hospitalization through Week 12 [ Time Frame: 12 weeks ]
    Participants with an event that results in admission to the hospital.
  • Percentage of participants with mucosal healing at Week 12 [ Time Frame: Week 12 ]
    Mucosal healing defined as endoscopic and histologic remission.
  • Ulcerative Colititis Symptom Questionnaire (UC-SQ): Change from Baseline to Week 12 [ Time Frame: Baseline, Week 12 ]
    The US-SQ is a patient questionnaire to assess severity of Crohn's symptoms.
  • Inflammatory Bowel Disease Questionnaire (IBDQ): Change from Baseline to Week 12 [ Time Frame: Baseline, Week 12 ]
    The IBDQ is used to assess the quality of life of patients with inflammatory bowel disease.
  • 36-Item Short Form Health Status Survey (SF-36): Change from Baseline to Week 12 [ Time Frame: Baseline, Week 12 ]
    The SF-36 is an indicator of overall health status.
  • Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue): Change from Baseline to Week 12 [ Time Frame: Baseline, Week 12 ]
    The FACIT-Fatigue is a validated tool that measures an individual's level of fatigue during their usual daily activities over the past week.
  • Percentage of participants with Ulcerative Colitis (UC)-related surgeries through Week 12 [ Time Frame: 12 weeks ]
    Participants who underwent surgery related to UC.
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE A Multicenter, Randomized, Double-Blind, Placebo Controlled Induction Study to Evaluate the Efficacy and Safety of Risankizumab in Subjects With Moderately to Severely Active Ulcerative Colitis Who Have Failed Prior Biologic Therapy
Official Title  ICMJE A Multicenter, Randomized, Double-Blind, Placebo Controlled Induction Study to Evaluate the Efficacy and Safety of Risankizumab in Subjects With Moderately to Severely Active Ulcerative Colitis Who Have Failed Prior Biologic Therapy
Brief Summary

The objectives of Sub-Study 1 are to evaluate the efficacy, safety, and pharmacokinetics of risankizumab as induction treatment in subjects with moderately to severely active ulcerative colitis (UC), and to identify the appropriate induction dose of risankizumab for further evaluation in Sub-Study 2.

The objective of Sub-Study 2 is to evaluate the efficacy and safety of risankizumab compared to placebo in inducing clinical remission in subjects with moderately to severely active UC.

Detailed Description Not Provided
Study Type  ICMJE Interventional
Study Phase  ICMJE Phase 2
Phase 3
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Condition  ICMJE Ulcerative Colitis (UC)
Intervention  ICMJE
  • Drug: risankizumab IV
    risankizumab intravenous (IV) infusion
    Other Names:
    • ABBV-066
    • BI 655066
  • Drug: placebo for risankizumab
    placebo for risankizumab
  • Drug: risankizumab SC
    risankizumab subcutaneous (SC) injection
    Other Names:
    • ABBV-066
    • BI 655066
Study Arms  ICMJE
  • Experimental: Substudy 1, Induction 2: Double-blind Risankizumab Dose 2
    Participants who received risankizumab with inadequate response in Induction 1 randomized to receive risankizumab dose 2 administered by subcutaneous (SC) injection in Induction 2.
    Intervention: Drug: risankizumab SC
  • Experimental: Substudy 2, Induction 1: Open-label Risankizumab Dose 2
    Participants randomized to receive risankizumab dose 2 administered by intravenous (IV) infusion.
    Intervention: Drug: risankizumab IV
  • Experimental: Substudy 2, Induction 2: Double-blind Risankizumab Dose 1(a)
    Participants who received placebo with inadequate response in Induction 1 randomized to receive risankizumab dose 1 administered by intravenous (IV) infusion in Induction 2.
    Intervention: Drug: risankizumab IV
  • Experimental: Substudy 2, Induction 2: Double-blind Risankizumab Dose 3
    Participants who received risankizumab with inadequate response in Induction 1 randomized to receive risankizumab dose 3 administered by subcutaneous (SC) injection in Induction 2.
    Intervention: Drug: risankizumab SC
  • Experimental: Substudy 1, Induction 1: Double-blind Risankizumab Dose 1
    Participants randomized to receive risankizumab dose 1 administered by intravenous (IV) infusion.
    Intervention: Drug: risankizumab IV
  • Experimental: Substudy 1, Induction 1: Double-blind Risankizumab Dose 2
    Participants randomized to receive risankizumab dose 2 administered by intravenous (IV) infusion.
    Intervention: Drug: risankizumab IV
  • Experimental: Substudy 1, Induction 2: Double-blind Risankizumab Dose 1(a)
    Participants who received placebo with inadequate response in Induction 1 receive risankizumab dose 1 administered by intravenous (IV) infusion in Induction 2.
    Intervention: Drug: risankizumab IV
  • Experimental: Substudy 1, Induction 2: Double-blind Risankizumab Dose 1(b)
    Participants who received risankizumab with inadequate response in Induction 1 randomized to receive risankizumab dose 1 administered by intravenous (IV) infusion in Induction 2.
    Intervention: Drug: risankizumab IV
  • Experimental: Substudy 2, Induction 1: Double-blind Risankizumab Dose 1
    Participants randomized to receive risankizumab dose 1 administered by intravenous (IV) infusion.
    Intervention: Drug: risankizumab IV
  • Experimental: Substudy 1, Induction 1: Double-blind Risankizumab Dose 3
    Participants randomized to receive risankizumab dose 3 administered by intravenous (IV) infusion.
    Intervention: Drug: risankizumab IV
  • Placebo Comparator: Substudy 1, Induction 1: Double-blind Placebo
    Participants randomized to receive placebo for risankizumab administered by intravenous (IV) infusion.
    Intervention: Drug: placebo for risankizumab
  • Experimental: Substudy 2, Induction 2: Double-blind Risankizumab Dose 2
    Participants who received risankizumab with inadequate response in Induction 1 randomized to receive risankizumab dose 2 administered by subcutaneous (SC) injection in Induction 2.
    Intervention: Drug: risankizumab SC
  • Experimental: Substudy 1, Induction 2: Double-blind Risankizumab Dose 3
    Participants who received risankizumab with inadequate response in Induction 1 randomized to receive risankizumab dose 3 administered by subcutaneous (SC) injection in Induction 2.
    Intervention: Drug: risankizumab SC
  • Placebo Comparator: Substudy 2, Induction 1: Double-blind Placebo
    Participants randomized to receive placebo for risankizumab administered by intravenous (IV) infusion.
    Interventions:
    • Drug: risankizumab IV
    • Drug: placebo for risankizumab
  • Experimental: Substudy 2, Induction 2: Double-blind Risankizumab Dose 1(b)
    Participants who received risankizumab with inadequate response in Induction 1 randomized to receive risankizumab dose 1 administered by intravenous (IV) infusion in Induction 2.
    Intervention: Drug: risankizumab IV
  • Experimental: Substudy 1, Induction 1: Open-label Risankizumab Dose 3
    Participants receive risankizumab dose 3 administered by intravenous (IV) infusion.
    Intervention: Drug: risankizumab IV
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Recruiting
Estimated Enrollment  ICMJE
 (submitted: January 8, 2018)
720
Original Estimated Enrollment  ICMJE Same as current
Estimated Study Completion Date  ICMJE August 29, 2022
Estimated Primary Completion Date September 23, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • Male or female aged >=18 to <= 80 years at the Baseline Visit. Where locally permissible, subjects 16 to < 18 years of age who meet the definition of Tanner stage 5 for development at the Baseline Visit
  • Confirmed diagnosis of ulcerative colitis (UC) for at least 3 months prior to Baseline.
  • Active UC as assessed by adapted Mayo Score
  • Demonstrated intolerance or inadequate response to one or more biologic therapies
  • Females must be postmenopausal for more than 2 years or surgically sterile or practicing specific forms of birth control.

Exclusion Criteria:

  • Subject with a current diagnosis of Crohn's disease (CD), inflammatory bowel disease-unclassified (IBD-U) or a history of radiation colitis or ischemic colitis.
  • Subject receiving prohibited medications and treatment.
  • Extent of inflammatory disease limited to the rectum as assessed by screening endoscopy.
  • Subject with currently known complications of UC (e.g., megacolon).
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 16 Years to 80 Years   (Child, Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE
Contact: ABBVIE CALL CENTER 847.283.8955 abbvieclinicaltrials@abbvie.com
Listed Location Countries  ICMJE Chile,   Russian Federation,   Argentina,   Austria,   Belgium,   Brazil,   Bulgaria,   Canada,   China,   Colombia,   Croatia,   Denmark,   Egypt,   France,   Germany,   Greece,   Israel,   Italy,   Japan,   Korea, Republic of,   Latvia,   Lithuania,   Malaysia,   Mexico,   Netherlands,   New Zealand,   Poland,   Portugal,   Puerto Rico,   Romania,   Serbia,   Singapore,   Slovakia,   Slovenia,   South Africa,   Spain,   Sweden,   Switzerland,   Taiwan,   Turkey,   Ukraine,   United Kingdom,   United States
Removed Location Countries American Samoa,   Australia,   Czechia,   Hungary
 
Administrative Information
NCT Number  ICMJE NCT03398148
Other Study ID Numbers  ICMJE M16-067
2016-004677-40 ( EudraCT Number )
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
IPD Sharing Statement  ICMJE
Plan to Share IPD: Yes
Plan Description: AbbVie is committed to responsible data sharing regarding the clinical trials we sponsor. This includes access to anonymized, individual and trial-level data (analysis data sets), as well as other information (e.g., protocols and clinical study reports), as long as the trials are not part of an ongoing or planned regulatory submission. This includes requests for clinical trial data for unlicensed products and indications.
Supporting Materials: Study Protocol
Supporting Materials: Statistical Analysis Plan (SAP)
Supporting Materials: Clinical Study Report (CSR)
Supporting Materials: Analytic Code
Time Frame: Data requests can be submitted at any time and the data will be accessible for 12 months, with possible extensions considered.
Access Criteria: Access to this clinical trial data can be requested by any qualified researchers who engage in rigorous, independent scientific research, and will be provided following review and approval of a research proposal and Statistical Analysis Plan (SAP) and execution of a Data Sharing Agreement (DSA). For more information on the process, or to submit a request, visit the following link.
URL: https://www.abbvie.com/our-science/clinical-trials/clinical-trials-data-and-information-sharing/data-and-information-sharing-with-qualified-researchers.html
Responsible Party AbbVie
Study Sponsor  ICMJE AbbVie
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Study Director: AbbVie Inc. AbbVie
PRS Account AbbVie
Verification Date December 2019

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP