Loading clinical trials...
Loading clinical trials...
Early therapeUtic RespOnse and Predictivity of Long-term Effectiveness of Upadacitinib in Ulcerative Colitis (EUROPE)
Ulcerative colitis (UC) is a type of inflammatory bowel disease that causes inflammation and bleeding from the lining of the rectum and colon (large intestine).This study will assess how effective upadacitinib is in treating UC. Upadacitinib (RINVOQ) is an approved drug for treating UC. Approximately 400 adult participants who are prescribed Upadacitinib by their physician in accordance with local label will be enrolled in Germany, Austria and Switzerland. Upadacitinib will be administered in accordance with the terms of the local marketing authorization, and treatment of participants will be determined solely by the investigator. Participants in the study will be followed for up to 2 years. There will be no additional burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic and only data which are routinely collected during a regular visit will be utilized for this study.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Kepler Universitaetsklinikum GmbH /ID# 251868
Linz, Upper Austria, Austria
Krankenhaus der Barmherzigen Brueder Wien /ID# 251867
Vienna, Vienna, Austria
Krankenhaus der Barmherzigen Brueder Salzburg /ID# 251869
Salzburg, Austria
Universitaetsklinik Heidelberg /ID# 249922
Heidelberg, Baden-Wurttemberg, Germany
Praxis fuer Gastroenterologie /ID# 249917
Heidelberg, Baden-Wurttemberg, Germany
Rems-Murr-Klinikum Winnenden /ID# 278791
Winnenden, Baden-Wurttemberg, Germany
Klinikum Augsburg /ID# 249979
Augsburg, Bavaria, Germany
Medizinisches Versorgunszentrum Dachau /ID# 249945
Dachau, Bavaria, Germany
TUM Klinikum rechts der Isar /ID# 262176
Munich, Bavaria, Germany
Dr.med. Johannes Behrendt Facharzt für Innere Medizin und Gastroenterologie /ID# 260516
Brandenburg, Brandenburg, Germany
Start Date
October 20, 2022
Primary Completion Date
August 1, 2027
Completion Date
August 1, 2027
Last Updated
February 3, 2026
400
ESTIMATED participants
Lead Sponsor
AbbVie
NCT07271069
NCT06975722
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07185009