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NCT04305145

Infliximab for Treatment of Immune Checkpoint Inhibitor Colitis

Active, Not Recruiting Phase 2

Description

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?

Eligibility Criteria

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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
  • 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
  • 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

Trial Information

NCT04305145
Active, Not Recruiting
Phase 2
42 participants
Aug 2020
Jun 2030