Not medical advice. Talk to your doctor and the trial team before making any decision about a clinical trial.
PSC Trial Watch
Crohn'sRecruiting

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

Some of the main requirements, copied from the record:

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

Main thing being measured

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

Official details

StatusRecruiting
PhasePhase 2 / Phase 3
Study typeInterventional
ConditionsCrohn Disease
Lead sponsorChildren's Hospital Medical Center, Cincinnati
CollaboratorsNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Janssen Scientific Affairs, LLC
Enrollment180 (estimated)
Start date2023-07-01
Primary completion (est.)2027-03-31
First posted2022-12-21
Last updated2026-05-05
Official titlePrecise Infliximab Exposure and Pharmacodynamic Control to Achieve Deep Remission in Pediatric Crohn's Disease
ClinicalTrials.gov IDNCT05660746

Interventions

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)

SiteCityCountrySite status
Children's Hospital of Los AngelesLos Angeles, CaliforniaUnited StatesRecruiting
Lucile Packard Children's Hospital StanfordPalo Alto, CaliforniaUnited StatesRecruiting
Rady Children's Hospital San DiegoSan Diego, CaliforniaUnited StatesRecruiting
Nemours Children's Health System-WilmingtonWilmington, DelawareUnited StatesRecruiting
Nemours Children's Health System-JacksonvilleJacksonville, FloridaUnited StatesRecruiting
Riley Hospital for ChildrenIndianapolis, IndianaUnited StatesRecruiting
Cincinnati Children's HospitalCincinnati, OhioUnited StatesRecruiting
Cleveland Clinic Children's HospitalCleveland, OhioUnited StatesRecruiting
Nationwide Children's HospitalColumbus, OhioUnited StatesRecruiting
Children's Specialty GroupNorfolk, VirginiaUnited StatesRecruiting
Medical College of Wisconsin, Children's of WisconsinMilwaukee, WisconsinUnited StatesRecruiting

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.