ClinConnect ClinConnect Logo
Search / Trial NCT05496348

Study of Oral Upadacitinib to Assess Change in Disease Activity in Adult Participants With Ulcerative Colitis

Launched by ABBVIE · Aug 9, 2022

Trial Information

Current as of October 15, 2025

Recruiting

Keywords

Ulcerative Colitis Uc Upadacitinib Upa Rinvoq

ClinConnect Summary

This clinical trial is studying the effectiveness of a medication called upadacitinib (brand name RINVOQ) for treating adults with ulcerative colitis (UC), a condition that causes inflammation and bleeding in the large intestine. About 400 adults from Germany, Austria, and Switzerland who are already prescribed upadacitinib will participate in this study. The aim is to see how well the medication works in reducing the symptoms of UC over a period of up to two years.

To be eligible for this trial, participants need to have a confirmed diagnosis of moderate to severe active ulcerative colitis and must be starting treatment with upadacitinib as determined by their doctor. Participants should also be able to communicate with the study staff and agree to continue providing information even after stopping the medication if necessary. Throughout the study, participants will have regular visits to their healthcare provider, but there will be no additional burdens beyond their usual care. This trial is currently recruiting participants, and it’s important to note that those with certain health issues or previous exposure to similar medications may not qualify.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Participants with an endoscopically confirmed diagnosis of active moderate to severe Ulcerative colitis (UC).
  • Participants initiating Upadacitinib (UPA) at the investigator's discretion as part of their routine clinical care; the decision to administer UPA must be made prior to and independent of documentation for the study and according to the approved local label.
  • Participants able to understand and communicate with the investigator and comply with the requirements of the study.
  • Participants willing to continue with study documentation after cessation of UPA.
  • Exclusion Criteria:
  • Participants with any contraindication to Upadacitinib (UPA).
  • Participants previously exposed to a Janus kinase (JAK) inhibitor.

About Abbvie

AbbVie is a global biopharmaceutical company dedicated to developing innovative therapies that address complex health challenges. Founded in 2013 as a spin-off from Abbott Laboratories, AbbVie focuses on key therapeutic areas, including immunology, oncology, neuroscience, and virology. The company is committed to advancing scientific research and delivering groundbreaking treatments that enhance patient outcomes and quality of life. With a robust pipeline and a strong emphasis on collaboration, AbbVie strives to transform the future of medicine through its commitment to clinical excellence and patient-centered approaches.

Locations

Heidelberg, Baden Wuerttemberg, Germany

Herne, Nordrhein Westfalen, Germany

Friedrichsthal, Saarland, Germany

Saarbrücken, Saarland, Germany

Berlin, Germany

Berlin, Germany

Berlin, Germany

Berlin, Germany

Dresden, Germany

Hettstedt, Germany

Karlsruhe, Germany

Kassel, Germany

Koblenz, Germany

Koblenz, Germany

Pirmasens, Germany

Potsdam, Germany

Tostedt, Germany

Berlin, Germany

Berlin, Germany

Bitterfeld Wolfen, Germany

Coesfeld, Germany

Erfurt, Germany

Frechen, Germany

Hamm, Germany

Kiel, Germany

Lübeck, Germany

Minden, Germany

Muenster, Germany

Oldenburg, Germany

Büdelsdorf, Schleswig Holstein, Germany

Berlin Zehlendorf, Germany

Berlin, Germany

Dachau, Germany

Freiburg Im Breisgau, Germany

Geldern, Germany

Hamburg, Germany

Hannover, Germany

Herne, Germany

Iserlohn, Germany

Kiel, Germany

Lueneburg, Germany

Magdeburg, Germany

Muenster, Germany

Rostock, Germany

Schmalkalden, Germany

Stuttgart, Germany

Frankfurt Am Main, Hessen, Germany

Frankfurt, Germany

Halle (Saale), Germany

Nuernberg, Germany

Vienna, Wien, Austria

Cologne, Nordrhein Westfalen, Germany

Lübeck, Schleswig Holstein, Germany

Lübeck, Schleswig Holstein, Germany

Jena, Thueringen, Germany

Jena, Thueringen, Germany

Altenholz, Germany

Darmstadt, Germany

Dresden, Germany

Dresden, Germany

Hannover, Germany

Schwerin, Germany

Salzburg, Austria

Altenholz, Schleswig Holstein, Germany

Brandenburg An Der Havel, Brandenburg, Germany

Blaubeuren, Germany

Leverkusen, Germany

Munich, Germany

Leipzig, Sachsen, Germany

Augsburg, Germany

Frankfurt, Germany

Heinsberg, Germany

Jena, Germany

Munich, Germany

Nürtingen, Germany

Würselen, Germany

Munich, Germany

Linz, Oberoesterreich, Austria

Heidelberg, Baden Wuerttemberg, Germany

Chemnitz, Germany

Solingen, Germany

Potsdam, Brandenburg, Germany

Leipzig, Sachsen, Germany

Berlin, Germany

Heilbronn, Germany

Jerichow, Germany

Linz, Oberoesterreich, Austria

Kassel, Germany

Neumuenster, Schleswig Holstein, Germany

Munich, Germany

Rostock, Mecklenburg Vorpommern, Germany

Worms, Rheinland Pfalz, Germany

Chemnitz, Saarland, Germany

Dachau, Saarland, Germany

Darmstadt, Saarland, Germany

Frankfurt, Saarland, Germany

Frankfurt, Saarland, Germany

Hannover, Saarland, Germany

Kassel, Saarland, Germany

Kiel, Saarland, Germany

Kiel, Saarland, Germany

Koblenz, Saarland, Germany

Lueneburg, Saarland, Germany

Minden, Saarland, Germany

Oldenburg, Saarland, Germany

Augsburg, Bayern, Germany

Wuppertal, Nordrhein Westfalen, Germany

Dachau, Bayern, Germany

Darmstadt, Hessen, Germany

Frankfurt, Hessen, Germany

Frankfurt, Hessen, Germany

Kassel, Hessen, Germany

Hannover, Niedersachsen, Germany

Lueneburg, Niedersachsen, Germany

Oldenburg, Niedersachsen, Germany

Minden, Nordrhein Westfalen, Germany

Koblenz, Rheinland Pfalz, Germany

Chemnitz, Sachsen, Germany

Dresden, Sachsen, Germany

Kiel, Schleswig Holstein, Germany

Kiel, Schleswig Holstein, Germany

Zurich, Zuerich, Switzerland

Zurich, Zuerich, Switzerland

Bern, Switzerland

Bern, Switzerland

Ludwigshafen Am Rhein, Rheinland Pfalz, Germany

Lübeck, Schleswig Holstein, Germany

Darmstadt, Hessen, Germany

Jerichow, Sachsen Anhalt, Germany

Kiel, Schleswig Holstein, Germany

Hamburg, Germany

Munich, Bayern, Germany

Hannover, Niedersachsen, Germany

Coesfeld, Nordrhein Westfalen, Germany

Chemnitz, Sachsen, Germany

Leipzig, Sachsen, Germany

Altenholz, Schleswig Holstein, Germany

Hanau, Germany

Lugano, Ticino, Switzerland

Zurich, Zuerich, Switzerland

Patients applied

0 patients applied

Trial Officials

ABBVIE INC.

Study Director

AbbVie

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials