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NCT04305145Active, not recruitingPhase 2

Infliximab for Treatment of Immune Checkpoint Inhibitor Colitis

Phase II Study of Infliximab for the Treatment of Immune Checkpoint Inhibitor Colitis

Source: ClinicalTrials.gov · Last updated 29 Oct 2026

Brief summary (registry, in English)

The goal of this clinical trial is to compare the safety and effectiveness of infliximab compared to steroids for the treatment of immune checkpoint inhibitor-induced colitis (ICI colitis) in patients with stage III/IV skin cancer. The main questions this study aims to answer are: * How many patients treated with infliximab experience steroid-free disease resolution after 7 weeks? * How many patients treated with steroids experience steroid-free disease resolution after 7 weeks?

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
42 (estimated)
First submitted
9 Mar 2020
Start date
31 Aug 2020
Primary completion date
30 Jun 2030
Lead sponsor
Massachusetts General Hospital
Diseases
Melanoma
NCT number
NCT04305145

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 42
  • From 31 Aug 2020 to the primary completion date, 30 Jun 2030
  • 2 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.

Prior treatment

  • Prior history of inflammatory colitis related to immune checkpoint inhibitors requiring treatment with \> 10 mg/day of prednisone or equivalent, or any other immunosuppressive medication
  • Concurrent immune-related Adverse Event (irAE) requiring treatment with systemic corticosteroids (dose equivalent of prednisone 10 mg/day or higher) or another systemic immune suppressing medication within the past 10 days
  • Current use of any immune suppressing biologic medication, or use within the last 4 weeks; immune stimulating medications such as checkpoint blockade are explicitly permitted
  • Current use of combination treatment with an investigation immunotherapy targeting a pathway other than PD-1 or PD-L1, concurrent chemotherapy, or targeted therapy
  • Previous adverse reaction to infliximab or corticosteroids
  • Prior history of inflammatory bowel disease, microscopic colitis or segmental colitis associated with diverticulosis
  • Received more than 3 doses of systemic corticosteroids, or receive dsystemic corticosteroids at a dose exceeding 2mg/kg methylprednisolone or equivalent, within 72 hours prior to endoscopy

Other illness

  • Colonic perforation or abscess present at the time of screening
  • History of Hepatitis B or C with a positive viral load, untreated mycobacterium tuberculosis, or active herpes zoster infection
  • Current bacterial infection requiring antibiotic treatment, or systemic fungal infection

Who the study is looking for

  • Age ≥ 18
  • Stage III/IV skin cancer
  • Treatment with CTLA-4 inhibitor alone or in combination with PD-1or PD-L1 blockade within the past 8 weeks
  • Clinically significant diarrhea resulting in the decision to pause immunotherapy treatment
  • Endoscopically visible colitis (Mayo 1-3) at the time of screening

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

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
Massachusetts General Hospital Cancer Center
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
Dana-Farber Cancer Institute
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

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