Skip to main content
OpenTrials
Completed

NCT Number: NCT02674308

Entyvio (Vedolizumab) Long Term Safety Study

The purpose of this study is to assess the long-term safety of vedolizumab versus other biologic agents in participants with Ulcerative Colitis (UC) or Crohn's Disease (CD).

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Krankenhaus Der Elisabethinen Linz Gmbh, Oberosterreich, Austria

Loading trial locations.

About this study

The drug being tested in this prospective, observational study is called vedolizumab. Vedolizumab is being used to treat people who have UC or CD. This study will look at the long-term safety of vedolizumab versus other biologic agents in participants with UC or CD. The study will enroll approximately 5000 participants. All participants enrolled in this will belong to one of the two treatment group:

  • Vedolizumab
  • Other Biologic Agents -adalimumab, certolizumab pegol.

Golimumab and infliximab. Study drugs will be prescribed by the physician according to local prescribing information in the participating countries. This multi-centre trial will be conducted worldwide. The overall time to participate in this study is 7 years. Participants will make visits at every 6 months to their treating physician.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed informed consent, by the participant or a legally acceptable representative.
  • Aged at least 18 years.
  • Initiating vedolizumab or another biologic agent for UC or CD.
  • Signed release form, by the participant or a legally acceptable representative, permitting abstraction of the participant's medical records at Baseline and during participation in the study.

Exclusion criteria

  • The participant is enrolled in a clinical trial in which treatment for CD or UC is managed through a protocol.
  • Prior treatment with vedolizumab.
  • Any other reason that, in the Investigator's opinion, makes the participant unsuitable to participate in this study.

Treatment and study plan

Vedolizumab

Drug

Other Biologic Agents

Other

Other biologic agents include: Adalimumab, Certolizumab pegol, Golimumab, and Infliximab

Primary outcomes

  1. Percentage of Participants with Adverse Events of Special Interest

    Time frame: 7 years

    Adverse events of special interest in this study includes serious and opportunistic infections, gastrointestinal infections, respiratory infections, other clinically significant infections: malignancies; infusion-related reactions and hypersensitivity, hepatic injury; psoriasis and other skin events, other SAEs and adverse reactions.

Secondary outcomes

  1. Disease Severity in Ulcerative Colitis (UC) Participants

    Time frame: Baseline and at every 6 months (up to 7 years)

    Disease severity will be measured using the Mayo score for ulcerative colitis and is ranged from 0 (normal or inactive disease) to 9 (severe disease) and calculated as the sum of 3 subscores: stool frequency, rectal bleeding and physician rating of disease activity, each ranged from 0 to 3 (0=normal, 1=mild, 2=moderate, 3=severe).

  2. Disease Severity in Crohn's Disease (CD) Participants

    Time frame: Baseline and at every 6 months (up to 7 years)

    Disease severity will be measured using the Harvey-Bradshaw Index (HBI) for crohn's disease. HBI is used in the assessment and quantification of symptoms and the present level of disease activity of participants with Crohn's disease. It is a validated clinical index for Crohn's disease,HBI score consists of clinical parameters of general well-being (0= very well 1=slightly below average, 2=poor, 3=very poor, 4=terrible); abdominal pain (0=none, 1=mild, 2=moderate, 3=severe); number of liquid stools per day; abdominal mass (0=none, 1=dubious, 2=definite, 3=tender); and complications (8 items: arthralgia, uveitis, erythema nodosum, aphthous ulcers, pyoderma gangrenosum, anal fissures, new fistula, abscess [score 1 per item]).Lower scores indicate better well-being. The scores are classified as: <5=remission, 5-7=mild disease, 8-16=moderate disease and >16=severe disease. Minimum score is 0 and no pre-specified maximum score as it depends on the number of liquid stools.

  3. Participant Reported Quality of Life Assessment Using Short Inflammatory Bowel Disease Questionnaire (SIBDQ)

    Time frame: Baseline and at every 6 months (up to 7 years)

    The Short IBD Questionnaire is an instrument used to assess quality of life and is a disease-specific health-related quality of life questionnaire, that consists of 10 questions, each question is scored on a scale from 1 (poor quality of life) to 7 (good quality of life). The scores are summed up and divided by 10 for a mean score ranging from 1 (poor quality of life) to 7 (good quality of life). A higher score indicates a better health-related quality of life.

  4. Participant Reported Quality of Life Assessment Using 12-Item Short Form Health Survey (SF-12)

    Time frame: Baseline and at every 6 months (up to 7 years)

    The SF-12 health questionnaire is a 12 question assessment of functional health and well-being. The survey asks about various health aspects, including physical functioning, role limitations due to physical health problems, bodily pain, general health, vitality, social functioning, role limitations due to emotional problems, and mental health (psychological distress and psychological well-being). Two summary measures are derived: the Physical and the Mental Health Component Summary. For each component summary, survey items were weighted and summed to create a summary score between 0 and 100 with higher score indicating better quality of life.

  5. Time to Treatment Discontinuation

    Time frame: Baseline and at every 6 months (up to 7 years)

    Time to discontinuation for Entyvio and the other biologic agents will be measured.

  6. Reasons for Treatment Discontinuation

    Time frame: Baseline and at every 6 months (up to 7 years)

    Reasons for discontinuations for Entyvio and the other biologic agents will be measured.

Sponsors and collaborators

Lead sponsor

Takeda

Industry

Registry information

Official study title

Entyvio (Vedolizumab) Long-term Safety Study: An International Observational Prospective Cohort Study Comparing Vedolizumab to Other Biologic Agents in Patients With Ulcerative Colitis or Crohn's Disease

Acronym: Entyvio PASS

Important dates

Study start
2015
Primary completion
2021
Study completion
2021
First posted
Feb 4, 2016
Registry last updated
Oct 31, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.