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Study identifier: NCT06758024 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

PROactive and Early Infliximab Monitoring and OPTimization in Inflammatory Bowel Disease

Condition: Inflammatory Bowel Disease (IBD) · Crohn Disease (CD) · Ulcerative Colitis (UC)  ·  Sponsor: Pontificia Universidad Catolica de Chile

PhaseNA
Planned participants72
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Infliximab (IFX) is a Food and Drug administration (FDA)-appoved monoclonal antibody medication targeting tumor necrosis factor (TNF) widely used in inflammatory bowel disease (IBD) to treat intestinal inflammation and improve patient's symptoms. Intravenous (iv) IFX is effective to treat hospitalized IBD patients with moderate-to-severe flares who fail iv corticosteroids (CS). However, about one-third of IBD patients do not respond to this medications and a half will loss the response after an initial response. Researchers have shown that most of these phenomena occur due to low IFX concentrations sometimes accompanied by the development of anti-drug antiboides (ADA) againts IFX. Blood concentrations of IFX are widely variable among IBD patients despite receiving the same weight-based dose. Several patient factors including laboratory parameters and severity of intestinal inflammation influence the way an individual's body proccesses and eliminate this type of medications. Dashboard software systems can take into account patient characteristics and IFX concentrations to modelate and facilitate dosing of IFX. By using pharmacokinetics (PK) models specifically developed to facilitate IFX dosing, these softwares can provide and recommend multiple dosing regimes to help the clinicians to select the appropriate dose to achieve target and optimal IFX concentrations. The goal of this clinical trial is to learn if early measuring of IFX blood concentrations and dashboard-guided IF…

This description comes directly from the study's public registry record.

Talk to the study team

Cristian Hernández-Rocha Cristian Hernández-Rocha, MD  ·  56-22-3543838  ·  caherna4@uc.cl

Carolina Pavez Carolina Pavez, MD  ·  56-22-3543838  ·  cdpavez@uc.cl

Always discuss trial participation with your own doctor first.

Locations (1)

Pontificia Universidad Catolica of ChileSantiago, ChileRecruiting

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Source record: clinicaltrials.gov/study/NCT06758024