Precise Infliximab Exposure and Pharmacodynamic Control
Phase 2 / Phase 3 · Testing RoadMAB and Infliximab · 11 sites · Children's Hospital Medical Center, Cincinnati
Official record & contacts on ClinicalTrials.gov ↗
In plain English
What this trial is testing
This study is testing RoadMAB (a device) and Infliximab (a drug) as a possible treatment. Condition(s) listed: Crohn Disease.
It is open-label: participants know what they are receiving.
Phase 3 studies are large studies comparing a treatment with placebo or standard care. They are often the last step before a company asks regulators for approval.
Who can join
- Ages 6 to 22
- Any sex
Some of the main requirements, copied from the record:
- 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)
Plus 6 more requirement(s). There are also 18 reasons someone might not be able to join (exclusion criteria). Only the trial team can confirm whether you qualify.
What's involved
- About 180 participants are expected to take part.
- Start date: 2023-07-01.
- Main results expected around 2027-03-31 (estimate from the record).
- 11 study sites listed (11 marked recruiting) in United States.
Main thing being measured
- Rate of Deep Remission (Week 52)
In the researchers’ words
Approximately 3 million people in the United States are living with inflammatory bowel disease, which includes Crohn's Disease (CD). There are limited treatment options approved for use in children and adults with Crohn's disease.
This is a short automatic summary built from the official record. A fuller plain-English card is coming; until then, please read the official record.
Questions to ask your doctor and the trial team
- Am I likely to qualify, given my health history?
- What would I have to do, and how often would I need to visit?
- Could I get a placebo? What happens to my current treatment?
- What are the possible risks and benefits?
- Are travel or other costs covered?
- What happens after the trial ends?
Official details
| Status | Recruiting |
|---|---|
| Phase | Phase 2 / Phase 3 |
| Study type | Interventional |
| Conditions | Crohn Disease |
| Lead sponsor | Children's Hospital Medical Center, Cincinnati |
| Collaborators | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Janssen Scientific Affairs, LLC |
| Enrollment | 180 (estimated) |
| Start date | 2023-07-01 |
| Primary completion (est.) | 2027-03-31 |
| First posted | 2022-12-21 |
| Last updated | 2026-05-05 |
| Official title | Precise Infliximab Exposure and Pharmacodynamic Control to Achieve Deep Remission in Pediatric Crohn's Disease |
| ClinicalTrials.gov ID | NCT05660746 |
Interventions
- RoadMAB (Device)
The RoadMAB Dashboard is a real-time decision support system that incorporates PK model-informed Bayesian estimation to provide precision dosing at the point of care. - Infliximab (Drug)
Conventional dosing. Induction: 5-7.5 mg/kg at 0, 2, and 6 weeks. Maintenance: 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. Precision dosing. 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 m…
Full eligibility criteria (from the record)
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
Locations (11)
| Site | City | Country | Site status |
|---|---|---|---|
| Children's Hospital of Los Angeles | Los Angeles, California | United States | Recruiting |
| Lucile Packard Children's Hospital Stanford | Palo Alto, California | United States | Recruiting |
| Rady Children's Hospital San Diego | San Diego, California | United States | Recruiting |
| Nemours Children's Health System-Wilmington | Wilmington, Delaware | United States | Recruiting |
| Nemours Children's Health System-Jacksonville | Jacksonville, Florida | United States | Recruiting |
| Riley Hospital for Children | Indianapolis, Indiana | United States | Recruiting |
| Cincinnati Children's Hospital | Cincinnati, Ohio | United States | Recruiting |
| Cleveland Clinic Children's Hospital | Cleveland, Ohio | United States | Recruiting |
| Nationwide Children's Hospital | Columbus, Ohio | United States | Recruiting |
| Children's Specialty Group | Norfolk, Virginia | United States | Recruiting |
| Medical College of Wisconsin, Children's of Wisconsin | Milwaukee, Wisconsin | United States | Recruiting |
For contacts at each site, use the official record.
Information only, not medical advice. Talk to your doctor and the trial team before making any decision about a clinical trial.