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NCT03765450Active, not recruiting

Pharmacokinetics of IFX and TNF Concentrations in Serum, Stool, and Colonic Mucosa in Acute Severe Ulcerative Colitis

Pharmacokinetics of Infliximab and Tumor Necrosis Factor Concentrations in Serum, Stool, and Colonic Mucosa in Acute Severe Ulcerative Colitis

Source: ClinicalTrials.gov · Last updated 2 Jun 2026

Brief summary (registry, in English)

This is an open-label, prospective, observational study with the primary objective to characterize the pharmacokinetics of infliximab in patients with Acute Severe Ulcerative Colitis.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
18 (actual)
First submitted
4 Dec 2018
Start date
21 Dec 2018
Primary completion date
22 Dec 2023
Lead sponsor
Alimentiv Inc.
NCT number
NCT03765450

What you commit to

  • Study type: Observational
  • Participants enrolled: 18
  • From 21 Dec 2018 to the primary completion date, 22 Dec 2023
  • 3 sites in 2 countries
  • 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.

Prior treatment

  • Prior enrollment in the current study.

Other illness

  • A known history of being positive for anti-IFX antibodies.
  • Have a serious active infection, active malignancy, or any other known condition contraindicated with infliximab therapy, according to current prescribing information.
  • Serious underlying disease other than ASUC, or other physical or psychosocial condition that, in the opinion of the investigator, may interfere with the subject's ability to participate fully in the study.

Who the study is looking for

  • Present to hospital with ASUC based on Truelove and Witts criteria,33 defined as the presence of more than 6 bloody stools per day along with any 1 of the following: tachycardia \> 90 beats per minute, fever \> 37.8 °C, hemoglobin \< 10.5 g/dL, and erythrocyte sedimentation rate (ESR) \> 30 mm/h (or CRP \> 30 mg/L \[high-sensitivity CRP \> 300 mg/L\]) is a suitable surrogate if ESR is not available1).
  • Have a partial MCS \> 7.
  • Have a Mayo Clinic ES ≥ 2 with disease extending 15 cm or more beyond the anal verge.
  • Require rescue inpatient IFX infusion as part of routine care. Note, the IFX treatment regimen is not defined by this protocol and any dosage regimen is acceptable for the purposes of this study, such as standard or accelerated induction regimens.
  • Be able to speak English and participate fully in all aspects of this clinical trial.
  • Provide written informed consent.

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

Full criteria on ClinicalTrials.gov

Sites (3)

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

SiteCityCountrySite status
Mount Sinai Hospital
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
Cornell University
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
UCSD
Coordinator of this site? Confirm its status
San DiegoUnited StatesUnknown status

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