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Clinical Trials/EUCTR2014-005376-29-NL
EUCTR2014-005376-29-NL
Active, not recruiting
Not Applicable

An open-label observational phase 4 study to evaluate efficacy , safety and mucosal healing of early versus late use of vedolizumab in Crohn's disease: the LOVE-CD study (LOw countries VEdolizumab in CD study) - LOVE-CD

Academic Medical Center, Gastroenterology0 sites260 target enrollmentJanuary 8, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Active Crohn's disease
Sponsor
Academic Medical Center, Gastroenterology
Enrollment
260
Status
Active, not recruiting
Last Updated
10 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 8, 2015
End Date
TBD
Last Updated
10 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Academic Medical Center, Gastroenterology

Eligibility Criteria

Inclusion Criteria

  • \- Established diagnosis of ileal, ileocolonic or colonic Crohn’s disease with histopathological confirmation available in the record of the patient.
  • \- Moderately to severely active CD (CDAI 220\-450\) with objective evidence of ulcerations visualized on endoscopy.
  • \- Anti\-TNF discontinued for at least 6 weeks
  • \-Age 18 to 80
  • \- GROUP 1 (EARLY CD):
  • Diagnosis of CD \< 24 months prior to enrollment
  • Demonstrated failure to respond to topical or systemic corticosteroids or intolerance to corticosteroids
  • or: need for \> 2 courses of steroids since diagnosis
  • or: steroid dependency at any dose since diagnosis
  • GROUP 2 (LATE CD)

Exclusion Criteria

  • \- Prior treatment with vedolizumab.
  • \- Contraindication for endoscopy.
  • \- History of colonic dysplasia/cancer
  • \- Presence of stoma
  • \- Received other biologics within the last 6 weeks of screening
  • \- Use of 5\-ASA or corticosteroid enemas/suppositories within 2 weeks of enrollment
  • \- Chronic hepatitis B or C infection
  • \- Evidence of or treatment for C. difficile infection or other intestinal pathogen at screening within 4 weeks prior to enrollment
  • \- Active or latent tuberculosis
  • \- Conditions which in the opinion of the investigator may interfere with the subject’s ability to comply with the study procedures.

Outcomes

Primary Outcomes

Not specified

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