Precise Infliximab Exposure and Pharmacodynamic Control (REMODEL-CD)
Crohn Disease
About this trial
This is an interventional treatment trial for Crohn Disease focused on measuring Crohn's
Eligibility Criteria
Inclusion Criteria: Written informed consent from the patient (≥18 years old) or from parent/legal guardian if patient is <18 years old Written informed assent from patient when age appropriate Diagnosis of Crohn's disease within the last 90 days (luminal-only or luminal with a perianal fistula or abscess treated with antibiotics for at least 7 days) ≥6 years to ≤22 years of age, anti-TNF naïve and starting infliximab Clinical activity and luminal inflammation, defined by both (1) and (2) (1) PCDAI≥10 (<18 years old) or CDAI ≥150 (≥18 years old) in last 60 days before the decision to start infliximab (2) SES-CD>6, or SES-CD>3 for isolated ileal disease (or a report of large intestinal ulcerations)* within the last 60 days or a fecal calprotectin >250 μg/g within last 60 days before the decision to start infliximab C-reactive protein >0.5 mg/dL in last 30 days and/or fecal calprotectin >250 μg/g within last 60 days before the decision to start infliximab Negative TB (tuberculosis) interferon-gamma release test and a negative urine pregnancy test for female patients (if menstruation has started) Exclusion Criteria: Diagnosis of ulcerative colitis or inflammatory bowel disease-unspecified Prior use of anti-TNF therapy (infliximab, adalimumab, certolizumab pegol, or golimumab) Internal (abdominal/pelvic) penetrating fistula(e) in last 180 days Intra-abdominal abscess/phlegmon/inflammatory mass in the last 180 days Active perianal abscess (receiving oral antibiotics for <7 days) Intestinal stricture (luminal narrowing with pre-stenotic dilation >3 cm) and surgery planned in the next 90 days Clostridium difficile infection or other intestinal infection in the last 1-week or a severe infection in the last 90 days. Severe infection is defined as requiring hospitalization for treatment or a vancomycin taper. Current hospitalization for complications of severe Crohn's disease Planned use of methotrexate or 6-mercaptopurine (azathioprine) during the induction (first 3 doses of infliximab) phase Current ileostomy, colostomy, ileoanal pouch, and/or previous extensive small bowel resection (>35 cm) or any CD surgery planned within the next 90 days History of autoimmune hepatitis, primary sclerosing cholangitis, thyroiditis, or juvenile idiopathic arthritis Treatment with another investigational drug in the last four weeks History of malignancy (including lymphoma or leukemia) Currently receiving treatment for histoplasmosis History of TB, human immunodeficiency virus (HIV), an immunodeficiency syndrome, a central nervous system demyelinating disease, history of heart failure or receiving intravenous antibiotics in last 14 days for any infection Currently pregnant, breast feeding or plans to become pregnant in the next 1 year Inability or failure to provide informed assent/consent Any developmental disabilities that would impede providing assent/consent
Sites / Locations
- Children's Hospital of Los Angeles
- Lucile Packard Children's Hospital Stanford
- Rady Children's Hospital San Diego
- Nemours Children's Health System-Wilmington
- Nemours Children's Health System-Jacksonville
- Riley Hospital for ChildrenRecruiting
- Cincinnati Children's HospitalRecruiting
- Cleveland Clinic Children's Hospital
- Nationwide Children's Hospital
- Medical College of Wisconsin, Children's of Wisconsin
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Conventional dosing
Precision dosing
Induction Phase: 5-7.5 mg/kg at 0, 2, and 6 weeks. Maintenance Phase : 5-10 mg/kg at every 4-8 weeks based on results of drug concentration monitoring for a flat target of 5-10 μg/mL.
Induction: 5-12.5 mg/kg at 0, 2, and 6 weeks to target a week6 concentration of 18-24 μg/mL with dosing support provided by the RoadMABTM clinical decision support tool. Maintenance: 5-15 mg/kg every 4-8 weeks to achieve apriori pharmacokinetic and pharmacodynamic targets (CRP, disease activity scores and fecal calprotectin) with dosing support provided by the RoadMABTM clinical decision support tool.