RecruitingPhase 2NCT06841705

Early Vedolizumab as First-Line for Immune-Related Colitis Therapy Trial

Early Concomitant Vedolizumab as First-Line for Immune-Related Colitis Therapy Trial


Sponsor

Shilpa Grover, MD, MPH

Enrollment

80 participants

Start Date

Jul 15, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to compare the effectiveness and safety of Vedolizumab with a short course of steroids compared to standard course of steroids for the treatment of immune checkpoint inhibitor colitis (ICI colitis) in adults. The main questions it aims to answer are: * How many patients treated with Vedolizumab and a short course of steroids experience resolution of colitis at 8 weeks. * How many patients treated with a standard course of steroids experience resolution of colitis at 8 weeks. Participants will: Recieve 3 doses of Vedolizumab or a placebo (a look-alike substance that contains no drug) infusions over 6 weeks Receive intravenous Medrol daily for 3 days Receive Prednisone daily for 7 days Receive Prednisone or placebo taper daily Receive Sulfamethoxazole-Trimethoprim or placebo taper daily Weekly checkups and periodic tests


Eligibility

Min Age: 18 Years

Inclusion Criteria6

  • Age ≥18 years.
  • Treatment with an ICI for cancer within the past 8 weeks.
  • Confirmed endoscopic/histologic diagnosis of ICI colitis.
  • Grade 2-3 diarrhea by Common Terminology Criteria for Adverse Events.
  • Willing and able to comply with the requirements of the protocol.
  • Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria19

  • Prior history of inflammatory colitis requiring treatment with greater than prednisone 10 mg daily or equivalent or any immunosuppressive medication.
  • Current or recent use of immunosuppressive biologic medication (for any reason including ICI colitis) within 4 weeks.
  • Concurrent immune-related adverse event requiring systemic steroids or systemic immunosuppression within 2 weeks.
  • Colonic perforation or abscess.
  • Partial or complete bowel obstruction within the last 3 months, signs/symptoms of bowel obstruction, or known radiologic evidence of impending obstruction.
  • Active Clostridium difficile or other colonic infection.
  • Concurrent hepatitis B or C infection.
  • History of untreated tuberculosis and/or positive quantiferon/Tspot test without previous tuberculosis prophylaxis, or untreated active infection with mycobacterium tuberculosis.
  • Active or known prior infection with nontuberculous mycobacteria (NTM).
  • Unable or unwilling to undergo a colonoscopy/flexible sigmoidoscopy.
  • Inpatient status, though patients can be screened while inpatients, they must be outpatient for the planned treatment of ICI colitis.
  • History of total proctocolectomy.
  • Female patients who are pregnant or breastfeeding or plan to become pregnant in the next 6 months.
  • Patients who are unable to give informed consent.
  • Previous SARS-CoV-2 infection within 10 days for mild infections or 20 days for severe/critical illness prior to first Vedolizumab dose.
  • Unable to adhere to protocol requirements.
  • Any condition that the physician investigators deem unsafe, including other conditions or medications that the investigator determines will put the subject at greater risk from vedolizumab plus brief course of steroids.
  • Allergy to sulfamethoxazole-trimethoprim.
  • Weight greater than 120 kg.

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Interventions

DRUGVedolizumab 300 MG Injection [Entyvio]

This is a biologic medication to treat colitis

DRUGPrednisone (and methylprednisolone)

This is a steroid

DRUGPrednisone Taper

This is a tapering dose of prednisone

OTHERPlacebo Prednisone Capsules

Placebo for Prednisone

OTHERPlacebo Vedolizumab

Placebo for Vedolizumab

OTHERSulfamethoxazole-Trimethoprim

Antibiotic if on \>21 days of steroids

DRUGPlacebo for Sulfamethoxazole-Trimethoprim

Placebo for antibiotic (Sulfamethoxazole-Trimethoprim) Antibiotic. Only if on \>21 days of prednisone/placebo


Locations(2)

Brigham and Women's Hospital

Boston, Massachusetts, United States

Dana Farber Cancer Institute

Boston, Massachusetts, United States

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NCT06841705