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
- Diseases
- Ulcerative colitis
- 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
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| General hospital Celje, Department of Gastoenterology Coordinator of this site? Confirm its status | Celje | Slovenia | Unknown status |
| General hospital Izola, Department of Internal medicine Coordinator of this site? Confirm its status | Izola | Slovenia | Unknown status |
| University Medical Centre Ljubljana, Department of Gastroenterology Coordinator of this site? Confirm its status | Ljubljana | Slovenia | Unknown status |
| University Medical Centre Maribor, Department of Gastoenterology Coordinator of this site? Confirm its status | Maribor | Slovenia | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.