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Individualized Infiximab Dosing-Proof of Concept Study

Individualized Infiximab Dosing-Proof of Concept Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02027727
Enrollment
56
Registered
2014-01-06
Start date
2013-11-30
Completion date
2018-03-31
Last updated
2017-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory Bowel Diseases

Keywords

inflammatory bowel disease, infliximab, trough level, crohn's disease, ulcerative colitis

Brief summary

The purpose of this study is to determine which early infliximab pharmacokinetic level is most associated with clinical remission at weeks 30 and 54 in pediatric IBD patients.

Detailed description

Our aims are: 1. to determine which early pk level; week 6 (peak), week 8 (2 week) or week 14 (trough), is most associated with week 30 and 54 outcomes in pediatric IBD patients. 2. to determine if the forecasted PK determined by a newly developed Population PK Model software program is in agreement with the observed PK in IBD patients receiving infliximab. Subject recruitment is limited to patients of the principal investigator only. Subjects will be approached for participation in the research in person during a routine clinic visit by a member of the study team.

Interventions

OTHERNo Intervention

no intervention- tihs is an observational study

Sponsors

Cedars-Sinai Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to 23 Years
Healthy volunteers
No

Inclusion criteria

1. Males and females on IFX 2. Patients with IBD 3. Age 6-23 4. Able to obtain consent

Exclusion criteria

1. Not receiving infliximab 2. On 10 mg/kg of IFX 3. Not able to obtain consent

Design outcomes

Primary

MeasureTime frameDescription
Infliximab level and clinical remission at 54 weeks54 weeksDetermine what level (peak, 2 week or trough) best correlates with clinical remission at week 54 Clinical remission definition: PCDAI \< 10 or CDAI \< 150 for Crohn's disease, or partial Mayo \<2 points and no sub-score \> 1 for ulcerative colitis. Fischer exact testing will be done to determine what detectable IFX level (week 6, week 8 or week 14) is most associated with week 54 clinical remission. Wilcoxon rank sum test will be performed to determine the median level that is most associated with week 54 clinical remission. Regression tree analysis will be performed to determine the optimal infliximab level cut point that predicts week 54 clinical remission.
Infliximab level and clinical remission at 30 weeks30 weeksDetermine what level (peak, 2 week or trough) best correlates with clinical remission at week 30 Clinical remission definition: PCDAI \< 10 or CDAI \< 150 for Crohn's disease, or partial Mayo \<2 points and no sub-score \> 1 for ulcerative colitis.

Secondary

MeasureTime frameDescription
Agreement between pk profiles predicted by the PK model and actual (measured) pk profiles1 yearSecondary outcomes 1. Agreement between pk profiles predicted by the PK model and actual (measured) pk profiles for all patients with at least 6 months in between levels Analysis: Bland Altman test will be used to quantify the agreement between the two methods: Software pk model vs actual measured pk profiles 2. Comparison of software selected dose regimens with actual dose regimens for cost and overall drug exposure (AUC and Cmax)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026