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Precise Infliximab Exposure and Pharmacodynamic Control (REMODEL-CD)

Primary Purpose

Crohn Disease

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
RoadMAB
Infliximab
Sponsored by
Children's Hospital Medical Center, Cincinnati
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn Disease focused on measuring Crohn's

Eligibility Criteria

6 Years - 22 Years (Child, Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Active Comparator

Experimental

Arm Label

Conventional dosing

Precision dosing

Arm Description

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.

Outcomes

Primary Outcome Measures

Rate of Deep Remission
Pediatric Crohn's disease activity index (PCDAI) <10 (child) or Crohn's disease activity index<150 (adult), off prednisone/budesonide for >8 weeks and Simple Endoscopic Scorer Crohn's Disease (SES-CD) SES-CD≤2

Secondary Outcome Measures

Rate of Steroid-free Clinical Remission
Pediatric Crohn's disease activity index (PCDAI) <10 (child) or Crohn's disease activity index<150 (adult) and off prednisone/budesonide for ≥4 weeks
Rate of Clinical Response
Decrease from baseline pediatric Crohn's disease activity index (PCDAI) of at least 12.5 points & total PCDAI<30 or a PCDAI<10 (child) or a reduction of Crohn's disease activity index>70 from baseline or CDAI<150 (adult)
Rate of Primary Clinical Nonresponse
On prednisone >16 consecutive weeks from start of infliximab or a pediatric Crohn's disease activity index>30 or CDAI>220 for first four infusions
Rate of Primary Biologic Nonresponse
Failure to improve baseline fecal calprotectin by >100 μg/g (limited to patients with a baseline fecal calprotectin >250 μg/g) or Failure to improve baseline c-reactive protein ≥0.5 mg/dL (limited to patients with a baseline c-reactive protein >1.0 mg/dL)
Rate of Sustained Steroid-free Remission
Pediatric Crohn's disease activity index (PCDAI)<10 (child) or Crohn's disease activity index<150 (adult) at dose5 to week52 and off prednisone/budesonide from week 22-52
Rate of Steroid-free Remission -biomarker composite
Pediatric Crohn's disease activity index (PCDAI)<10 (child) or Crohn's disease activity index<150 (adult), off prednisone/budesonide for ≥4 weeks, CRP≤0.5 mg/dL and fecal calprotectin <250 μg/g3
Rate of Endoscopic Healing
Simple endoscopic score-Crohn's disease ≤2
Rate of Complete Endoscopic Healing
Simple endoscopic score-Crohn's disease=0
Rate of Endoscopic Remission
Simple endoscopic score-Crohn's disease<4
Rate of Mucosal Healing
Simple endoscopic score-Crohn's disease ≤2 and Ileal Global Histologic Activity Score (GHAS)/ Colon Global Histologic Activity Score (CGHAS) ≤2
PK Model Bias
Model predicted vs. actual infliximab concentration Bias: mean predictive error (MPE)
PK Model Precision
Model predicted vs. actual infliximab concentration Precision: root mean squared error (RMSE)
Rate of IBD related event - Fistula
Occurrence of fistula and presence of antibody to infliximab >200 ng/mL
Rate of IBD related - Hospitalization
Occurrence of Crohn's disease related hospitalization
Rate of IBD related event - Surgery
Occurrence of Crohn's disease related Surgery
Rate of IBD related event - Intestinal stricture
Occurrence of Crohn's disease related intestinal stricture
Rate of IBD related event - Starting corticosteroids
Occurrence of subjects starting a corticosteroid after week20
Rate of IBD related event - Antibodies to infliximab
Occurrence of antibodies to infliximab defined as >200 ng/mL
Rate of Growth Restoration - Weight change
In Tanner stage I-III subjects: change in baseline weight (kg) by gender and age group
Rate of Growth Restoration- Height velocity
In Tanner stage I-III subjects: change in height velocity (zscore) by gender
PK of infliximab in pediatric patients
Measured infliximab clearance at baseline and at week52
Correlation between infliximab induction exposure and endoscopic remission
The correlation analysis to be performed for the total area under the curve (infliximab exposure, μg*h/mL from week0-week14) and patients achieving endoscopic remission. Endoscopic remission is defined as a Simple Endoscopic Scorer Crohn's Disease (SES-CD) ≤2.
Correlation between infliximab induction exposure and deep remission
The correlation analysis to be performed for the total area under the curve (infliximab exposure, μg*h/mL from week0-week14) and patients in deep remission. Deep remission is defined as a Pediatric Crohn's disease activity index (PCDAI) <10 (child) or Crohn's disease activity index<150 (adult), off prednisone/budesonide for >8 weeks and Simple Endoscopic Scorer Crohn's Disease (SES-CD) ≤2.
Patient Reported Outcome-2 (PRO2) Response
defined as a >50% improvement in total score from baseline
Patient Reported Outcome-2 (PRO2) Remission
defined as a stool frequency ≤3.0 and abdominal pain ≤1.0 (from baseline)
Quality of Life & Disability -IMPACT-III score
Total IMPACT-III (child) score
Quality of Life & Disability - Inflammatory Bowel Disease Disk score
Total Inflammatory Bowel Disease Disk (without sexual function assessment) score
Quality of Life & Disability - Short Inflammatory Bowel Disease score
Total Short IBD Questionnaire (adult) score
Process Evaluation -Usability of Decision Support Tool
Total System Usability Scale score
Rate of Adverse events
Number of Adverse Events
Rate of Serious Adverse events
Number of Serious Adverse Events

Full Information

First Posted
November 29, 2022
Last Updated
July 19, 2023
Sponsor
Children's Hospital Medical Center, Cincinnati
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Janssen Scientific Affairs, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT05660746
Brief Title
Precise Infliximab Exposure and Pharmacodynamic Control
Acronym
REMODEL-CD
Official Title
Precise Infliximab Exposure and Pharmacodynamic Control to Achieve Deep Remission in Pediatric Crohn's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2023 (Actual)
Primary Completion Date
March 31, 2027 (Anticipated)
Study Completion Date
March 31, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital Medical Center, Cincinnati
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Janssen Scientific Affairs, LLC

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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. Physicians need better ways to inform decisions on treatment. The main reason for this research study is to determine if a computer program that calculates an individualized dose based on a patient's blood testing results (precision dosing) can better achieve the best possible response to infliximab compared to standard dosing (conventional dosing).
Detailed Description
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)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn Disease
Keywords
Crohn's

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Patients newly diagnosed with Crohn's disease (ages 6-22 years inclusive) within the last 90 days AND starting infliximab
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
180 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conventional dosing
Arm Type
Active Comparator
Arm Description
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.
Arm Title
Precision dosing
Arm Type
Experimental
Arm Description
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.
Intervention Type
Device
Intervention Name(s)
RoadMAB
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
Infliximab
Other Intervention Name(s)
Avsola, Inflectra, Ixifi, Remicade, Renflexis
Intervention Description
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 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.
Primary Outcome Measure Information:
Title
Rate of Deep Remission
Description
Pediatric Crohn's disease activity index (PCDAI) <10 (child) or Crohn's disease activity index<150 (adult), off prednisone/budesonide for >8 weeks and Simple Endoscopic Scorer Crohn's Disease (SES-CD) SES-CD≤2
Time Frame
Week 52
Secondary Outcome Measure Information:
Title
Rate of Steroid-free Clinical Remission
Description
Pediatric Crohn's disease activity index (PCDAI) <10 (child) or Crohn's disease activity index<150 (adult) and off prednisone/budesonide for ≥4 weeks
Time Frame
Week 14 and Week 52
Title
Rate of Clinical Response
Description
Decrease from baseline pediatric Crohn's disease activity index (PCDAI) of at least 12.5 points & total PCDAI<30 or a PCDAI<10 (child) or a reduction of Crohn's disease activity index>70 from baseline or CDAI<150 (adult)
Time Frame
Week 14 and Week 52
Title
Rate of Primary Clinical Nonresponse
Description
On prednisone >16 consecutive weeks from start of infliximab or a pediatric Crohn's disease activity index>30 or CDAI>220 for first four infusions
Time Frame
Week 16
Title
Rate of Primary Biologic Nonresponse
Description
Failure to improve baseline fecal calprotectin by >100 μg/g (limited to patients with a baseline fecal calprotectin >250 μg/g) or Failure to improve baseline c-reactive protein ≥0.5 mg/dL (limited to patients with a baseline c-reactive protein >1.0 mg/dL)
Time Frame
Week 16
Title
Rate of Sustained Steroid-free Remission
Description
Pediatric Crohn's disease activity index (PCDAI)<10 (child) or Crohn's disease activity index<150 (adult) at dose5 to week52 and off prednisone/budesonide from week 22-52
Time Frame
Week 22 - Week 52
Title
Rate of Steroid-free Remission -biomarker composite
Description
Pediatric Crohn's disease activity index (PCDAI)<10 (child) or Crohn's disease activity index<150 (adult), off prednisone/budesonide for ≥4 weeks, CRP≤0.5 mg/dL and fecal calprotectin <250 μg/g3
Time Frame
Week 14 and Week 52
Title
Rate of Endoscopic Healing
Description
Simple endoscopic score-Crohn's disease ≤2
Time Frame
Week 52
Title
Rate of Complete Endoscopic Healing
Description
Simple endoscopic score-Crohn's disease=0
Time Frame
Week 52
Title
Rate of Endoscopic Remission
Description
Simple endoscopic score-Crohn's disease<4
Time Frame
Week 52
Title
Rate of Mucosal Healing
Description
Simple endoscopic score-Crohn's disease ≤2 and Ileal Global Histologic Activity Score (GHAS)/ Colon Global Histologic Activity Score (CGHAS) ≤2
Time Frame
Week 52
Title
PK Model Bias
Description
Model predicted vs. actual infliximab concentration Bias: mean predictive error (MPE)
Time Frame
Week 0 - Week 84
Title
PK Model Precision
Description
Model predicted vs. actual infliximab concentration Precision: root mean squared error (RMSE)
Time Frame
Week 0 - Week 84
Title
Rate of IBD related event - Fistula
Description
Occurrence of fistula and presence of antibody to infliximab >200 ng/mL
Time Frame
Week 0 - Week 52
Title
Rate of IBD related - Hospitalization
Description
Occurrence of Crohn's disease related hospitalization
Time Frame
Week 0 - Week 52
Title
Rate of IBD related event - Surgery
Description
Occurrence of Crohn's disease related Surgery
Time Frame
Week 0 - Week 52
Title
Rate of IBD related event - Intestinal stricture
Description
Occurrence of Crohn's disease related intestinal stricture
Time Frame
Week 0 - Week 52
Title
Rate of IBD related event - Starting corticosteroids
Description
Occurrence of subjects starting a corticosteroid after week20
Time Frame
Week 0 - Week 52
Title
Rate of IBD related event - Antibodies to infliximab
Description
Occurrence of antibodies to infliximab defined as >200 ng/mL
Time Frame
Week 0 - Week 52
Title
Rate of Growth Restoration - Weight change
Description
In Tanner stage I-III subjects: change in baseline weight (kg) by gender and age group
Time Frame
Week 14 - Week 52
Title
Rate of Growth Restoration- Height velocity
Description
In Tanner stage I-III subjects: change in height velocity (zscore) by gender
Time Frame
Week 14 - Week 52
Title
PK of infliximab in pediatric patients
Description
Measured infliximab clearance at baseline and at week52
Time Frame
Week 0 - Week 52
Title
Correlation between infliximab induction exposure and endoscopic remission
Description
The correlation analysis to be performed for the total area under the curve (infliximab exposure, μg*h/mL from week0-week14) and patients achieving endoscopic remission. Endoscopic remission is defined as a Simple Endoscopic Scorer Crohn's Disease (SES-CD) ≤2.
Time Frame
Exposure Week 0 - Week 14, Efficacy Week 54
Title
Correlation between infliximab induction exposure and deep remission
Description
The correlation analysis to be performed for the total area under the curve (infliximab exposure, μg*h/mL from week0-week14) and patients in deep remission. Deep remission is defined as a Pediatric Crohn's disease activity index (PCDAI) <10 (child) or Crohn's disease activity index<150 (adult), off prednisone/budesonide for >8 weeks and Simple Endoscopic Scorer Crohn's Disease (SES-CD) ≤2.
Time Frame
Exposure Week 0 - Week 14, Efficacy Week 54
Title
Patient Reported Outcome-2 (PRO2) Response
Description
defined as a >50% improvement in total score from baseline
Time Frame
Week 6, Week 14, Week 26, Week 52
Title
Patient Reported Outcome-2 (PRO2) Remission
Description
defined as a stool frequency ≤3.0 and abdominal pain ≤1.0 (from baseline)
Time Frame
Week 6, Week 14, Week 26, Week 52
Title
Quality of Life & Disability -IMPACT-III score
Description
Total IMPACT-III (child) score
Time Frame
Week 52
Title
Quality of Life & Disability - Inflammatory Bowel Disease Disk score
Description
Total Inflammatory Bowel Disease Disk (without sexual function assessment) score
Time Frame
Week 52
Title
Quality of Life & Disability - Short Inflammatory Bowel Disease score
Description
Total Short IBD Questionnaire (adult) score
Time Frame
Week 52
Title
Process Evaluation -Usability of Decision Support Tool
Description
Total System Usability Scale score
Time Frame
Week 0 - Week 52
Title
Rate of Adverse events
Description
Number of Adverse Events
Time Frame
Week 0 - Week 52
Title
Rate of Serious Adverse events
Description
Number of Serious Adverse Events
Time Frame
Week 0 - Week 52

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
22 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Phillip Minar, MD, MS
Phone
513-636-4415
Email
phillip.minar@cchmc.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Phillip Minar, MD,MS
Organizational Affiliation
Children's Hospital Medical Center, Cincinnati
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital of Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mallory Chavannes
First Name & Middle Initial & Last Name & Degree
Mallory Chavannes, MD
Facility Name
Lucile Packard Children's Hospital Stanford
City
Palo Alto
State/Province
California
ZIP/Postal Code
94304
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alka Goyal
First Name & Middle Initial & Last Name & Degree
Alka Goyal, MD
Facility Name
Rady Children's Hospital San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92123
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laura Bauman
First Name & Middle Initial & Last Name & Degree
Laura Bauman, MD
Facility Name
Nemours Children's Health System-Wilmington
City
Wilmington
State/Province
Delaware
ZIP/Postal Code
19803
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zarela Molle-Rios
First Name & Middle Initial & Last Name & Degree
Zarela Molle-Rios, MD
Facility Name
Nemours Children's Health System-Jacksonville
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jill Dorsey
First Name & Middle Initial & Last Name & Degree
Jill Dorsey, MD
Facility Name
Riley Hospital for Children
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Steven Steiner
First Name & Middle Initial & Last Name & Degree
Steven Steiner, MD
Facility Name
Cincinnati Children's Hospital
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kimberly Jackson
Email
kimberly.jackson@cchmc.org
First Name & Middle Initial & Last Name & Degree
Phillip Minar, MD, MS
Facility Name
Cleveland Clinic Children's Hospital
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jacob Kurowski
First Name & Middle Initial & Last Name & Degree
Jacob Kurowski, MD
Facility Name
Nationwide Children's Hospital
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43205
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brendan Boyle
First Name & Middle Initial & Last Name & Degree
Brendan Boyle
Facility Name
Medical College of Wisconsin, Children's of Wisconsin
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53226
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joshua Noe
First Name & Middle Initial & Last Name & Degree
Joshua Noe, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Precise Infliximab Exposure and Pharmacodynamic Control

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