To Evaluate the Safety and Efficacy of Remsima™ in Patients With Crohn's Disease (CD) or Ulcerative Colitis (UC)

NCT02326155 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 470

Last updated 2022-02-21

Study results available
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Summary

An observational, prospective cohort study to evaluate the safety and efficacy of Remsima™ in patients with Crohn's disease (CD) or Ulcerative Colitis (UC)

Conditions

Sponsors & Collaborators

Principal Investigators

  • Pavel Svoboda · Ostrava, Morvskoslezsky kraj, Czech Republic, 708 52

Eligibility

Min Age
6 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-12-08
Primary Completion
2020-02-28
Completion
2020-02-28

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02326155 on ClinicalTrials.gov