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NCT Number: NCT04775732

Ultra-proactive Therapeutic Drug Monitoring in Inflammatory Bowel Disease

This is a comparative pragmatic trial in patients with UC and CD on maintenance treatment with IFX. All IBD patients from cohort A with maintenance IFX treatment at a referral IBD clinic are prospectively included between June and August 2018. An ultra-proactive IFX TDM algorithm is applied as follows. All patients have an ELISA TL measurement at baseline, of which the result determined the follow-up pathway: (A) TL between 3-7μg/mL: continuation at same dose and interval; (B) TL >7μg/mL: interval prolongation allowed; (C) TL <3μg/mL: interval shortening with minimum 2 weeks, with the next IFX TL measured using a POCT. (i) If the POCT showed an IFX TL <3μg/mL, dose was optimized ad hoc using a linear dosing formula (Dosen = (TL target * Dose n-1) / TL measured), followed by a new POCT test at next visit with the same interval. (ii) If the POCT showed an IFX TL ≥3µg/mL, no additional dose was given and routine TL testing with ELISA was retaken at next visit. At every visit this algorithm was reapplied to all patients.

The patients from cohort A will be compared with the patients from cohort B. The patients in cohort B receive maintenance IFX treatment at a referral IBD clinic during the same period. Dose adjustment are done based on standard of care reactive TDM of IFX and clinical symptoms. Data will be collected retrospectively to avoid treatment optimization bias.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Imelda GI clinical research center, Bonheiden, Belgium

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • all adult IBD patients treated for at least 14 weeks with infliximab were included

Exclusion criteria

  • induction treatment with infliximab (<14 weeks)
  • treatment with other biological for IBD

Treatment and study plan

infliximab therapeutic drug monitoring

Biological

dose optimization of infliximab based on a predefined dosing algorithm

Primary outcomes

  1. number of patients with infliximab failure

    Time frame: one year

    number of patients with infliximab failure after one year (infliximab failure = infliximab discontinuation, IBD related surgery, IBD related hospitalization, add-on IBD treatment, and allergic reaction to infliximab)

Secondary outcomes

  1. number of TL measurements per patient per year

    Time frame: one year

  2. percentage of interval changes (shortening, prolongation, bidirectional)

    Time frame: one year

  3. number of patients with infliximab discontinuation

    Time frame: one year

    number of patients with discontinuation of infliximab

  4. percentage of patients with sustained clinical remission

    Time frame: one year

    number of patients with physician global assessment <1 and all visits

  5. number of patients with mucosal remission

    Time frame: one year

    number of patients with mucosal remission after one year. (Mucosal remission = simple endoscopic score for CD <3, Rutgeertscore <i2 for, Mayo endoscopic subscore <1 and faecal calprotectin <250 µg/ml. Endoscopy and/or faecal calprotectin between 6 and 12 months after inclusion. If endoscopy and faecal calprotectin at the same moment, then endoscopy was dominant)

Sponsors and collaborators

Lead sponsor

Imelda GI Clinical Research Center

Other

Registry information

Official study title

Ultra-proactive Therapeutic Drug Monitoring of Infliximab Based on Point-of-care-testing in Inflammatory Bowel Disease: a Pragmatic Trial

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Mar 1, 2021
Registry last updated
Aug 5, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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