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Precise Infliximab Exposure and Pharmacodynamic Control

NCT05660746 · Children's Hospital Medical Center, Cincinnati
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Official title
Precise Infliximab Exposure and Pharmacodynamic Control to Achieve Deep Remission in Pediatric Crohn's Disease
About this study
This is an open-label, cluster randomized clinical trial to test whether precision infliximab dosing with a targeted concentration intervention is superior in achieving deep remission (endoscopic healing and clinical remission) compared to patients receiving conventional infliximab dosing. With recognition that CD patients who achieve the "target" of deep remission with anti-TNF dose optimizations following pharmacodynamic monitoring had a significant reduction in CD-related adverse events, our central hypothesis is precision dosing with infliximab during induction and maintenance will achieve superior rates of deep remission vs. conventional care (control arm)
Eligibility criteria
Inclusion Criteria: 1. Written informed consent from the patient (≥18 years old) or from parent/legal guardian if patient is \<18 years old 2. Written informed assent from patient when age appropriate 3. 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) 4. ≥6 years to ≤22 years of age, anti-TNF naïve and starting infliximab 5. 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 75 days prior to screening 6. C-reactive protein \>1.0 mg/dL in last 30 days and/or fecal calprotectin \>250 μg/g within last 75 days prior to screening 7. Negative TB (tuberculosis) interferon-gamma release test and a negative urine pregnancy test for female patients (if menstruation has started) Exclusion Criteria: 1. Diagnosis of ulcerative colitis or inflammatory bowel disease-unspecified 2. Prior use of anti-TNF therapy (infliximab, adalimumab, certolizumab pegol, or golimumab) 3. Internal (abdominal/pelvic) penetrating fistula(e) in last 180 days 4. Intra-abdominal abscess/phlegmon/inflammatory mass in the last 180 days 5. Active perianal abscess (receiving oral antibiotics for \<7 days) 6. Intestinal stricture (luminal narrowing with pre-stenotic dilation \>3 cm) and surgery planned in the next 90 days 7. Have tested positive for Clostridium difficile toxin (stool assay) or other intestinal pathogens within 14 days of screening unless a repeat examination is negative and there are no signs of ongoing infection with that pathogen. 8. Current hospitalization for complications of severe Crohn's disease 9. Planned use of methotrexate or 6-mercaptopurine (azathioprine) during the induction (first 3 doses of infliximab) phase 10. Current ileostomy, colostomy, ileoanal pouch, and/or previous extensive small bowel resection (\>35 cm) or any CD surgery planned within the next 90 days 11. History of autoimmune hepatitis, primary sclerosing cholangitis, thyroiditis, or juvenile idiopathic arthritis 12. Treatment with another investigational drug in the last four weeks 13. History of malignancy (including lymphoma or leukemia) 14. Currently receiving treatment for histoplasmosis 15. 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 16. Currently pregnant, breast feeding or plans to become pregnant in the next 1 year 17. Inability or failure to provide informed assent/consent 18. Any developmental disabilities that would impede providing assent/consent
Study design
Enrollment target: 180 participants
Allocation: non_randomized
Masking: none
Age groups: child, adult
Timeline
Starts: 2023-07-01
Estimated completion: 2027-03-31
Last updated: 2025-01-31
Interventions
Device: RoadMABDrug: Infliximab
Primary outcomes
  • Rate of Deep Remission (Week 52)
Sponsor
Children's Hospital Medical Center, Cincinnati · other
With: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Janssen Scientific Affairs, LLC
Contacts & investigators
ContactPhillip Minar, MD, MS · contact · phillip.minar@cchmc.org · 513-636-4415
InvestigatorPhillip Minar, MD,MS · principal_investigator, Children's Hospital Medical Center, Cincinnati
All locations (11)
Children's Hospital of Los AngelesRecruiting
Los Angeles, California, United States
Lucile Packard Children's Hospital StanfordRecruiting
Palo Alto, California, United States
Rady Children's Hospital San DiegoRecruiting
San Diego, California, United States
Nemours Children's Health System-WilmingtonRecruiting
Wilmington, Delaware, United States
Nemours Children's Health System-JacksonvilleRecruiting
Jacksonville, Florida, United States
Riley Hospital for ChildrenRecruiting
Indianapolis, Indiana, United States
Cincinnati Children's HospitalRecruiting
Cincinnati, Ohio, United States
Cleveland Clinic Children's HospitalRecruiting
Cleveland, Ohio, United States
Nationwide Children's HospitalRecruiting
Columbus, Ohio, United States
Children's Specialty GroupRecruiting
Norfolk, Virginia, United States
Medical College of Wisconsin, Children's of WisconsinRecruiting
Milwaukee, Wisconsin, United States
Precise Infliximab Exposure and Pharmacodynamic Control · TrialPath