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NCT04156984CompletedPhase 4

Comparison of Two Different Golimumab Dosing Regimens for Ulcerative Colitis

Exposure-response of Golimumab During Maintenance in Ulcerative Colitis: An Exploratory Pharmacokinetics/Pharmacodynamics Comparison of Different Dose Regimens

Source: ClinicalTrials.gov · Last updated 30 Jul 2024

Brief summary (registry, in English)

Partial response or loss of response to golimumab is observed in a significant proportion of patients started on golimumab for active ulcerative colitis. The current dosing regimen in European Union is based on patients' body weight as maintenance treatment for patients with ≥ 80 kg is 100 mg q4 weeks and for patients with \<80 kg 50 mg q4 weeks. The investigators recent observations in a golimumab pharmacokinetics study of 24 patients however, show large interindividual variations in golimumab trough concentrations. Furthermore, it seems that patients with continuous response have higher golimumab trough levels at several time points during treatment compared to patients who lose response. Higher induction/maintenance dose of golimumab increases golimumab trough levels, therefore it is likely that higher induction/maintenance dose of golimumab would increase efficacy of golimumab treatment.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
27 (actual)
First submitted
24 Oct 2019
Start date
7 Apr 2021
Primary completion date
18 Jun 2024
Lead sponsor
David Drobne
NCT number
NCT04156984

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 27
  • From 7 Apr 2021 to the primary completion date, 18 Jun 2024
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Active tuberculosis or other opportunistic bacterial, viral and fungal infections
  • History of moderate to severe heart failure (NYHA III/IV), and potential risk of congestive heart failure
  • History of allergic reactions to sorbitol (E420), L-histidine, L-histidine monohydrochloride monohydrate, polysorbate80, water for injections.

Other

  • Pregnancy

Who the study is looking for

  • Histologically confirmed ulcerative colitis

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
General hospital Celje, Department of Gastoenterology
Coordinator of this site? Confirm its status
CeljeSloveniaUnknown status
General hospital Izola, Department of Internal medicine
Coordinator of this site? Confirm its status
IzolaSloveniaUnknown status
University Medical Centre Ljubljana, Department of Gastroenterology
Coordinator of this site? Confirm its status
LjubljanaSloveniaUnknown status
University Medical Centre Maribor, Department of Gastoenterology
Coordinator of this site? Confirm its status
MariborSloveniaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.