Infliximab Accelerated Induction in Moderate to Severe Pediatric UC

NCT ID: NCT03209232

Last Updated: 2021-10-01

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-04-16
• Study Completion Date: 2021-09-01

Brief Summary

Objectives: To examine the effect of accelerated infliximab induction in children with moderate to severe UC. Design: A multi-center, prospective, randomized, open label study. Setting: Pediatric gastroenterology centers. Participants: Children 6 year to 17 years (Overall, 84 patients) with moderate to severe UC who are corticosteroid dependent/resistant thus planned to receive infliximab induction. Intervention: Group 1 (intervention) will receive an accelerated induction at 0,1,3 weeks (5 mg/kg) and then at week 7,11,15. Group 2 (standard) will receive a per protocol induction at 0,2,6 weeks (5 mg/kg) and then at week 14. Drug levels will be obtained prior to each infusion in each group (up to week 20). Further maintenance will be planned according to drug levels at weeks 15 and 14, respectively. Follow-up will continue without further interventions till 52 weeks following induction. Main outcome measure: Clinical remission, on infliximab at week 20. Secondary outcome measures: 1. Colectomy free rates at week 20 and 52. 2. Clinical remission on infliximab at week 52. 3. Drug levels and anti-drug antibodies prior to last study infusion. 4. Anthropometric and laboratory measures including calprotectin at the end of induction, week 20 and week 52 5. Changes in fecal microbiome, virome and bile acids content. Sample size: In order to demonstrate 30% difference in clinical remission rate between groups is significant, we will need to study 36 children in each group to be able to reject the null hypothesis that the failure rates between the groups are equal with probability (power) of 80% and a type I error probability of 0.05.

Detailed Description

General intervention scheme:

The decision to start IFX is the sole decision of the treating physician based on the patient's immediate need. Eligible patients are those who are planned to start IFX. All patients will undergo clinical and laboratory evaluation for IFX eligibility (PPD, infectious serology). If the tests have already done in the last 3 months, we will use these data, there is no need to repeat. Patients must have a negative stool culture, stool for parasites and clostridium difficile toxin test performed over the last week in order to be eligible. The screening visit may be performed concomitantly with the enrolment visit if all inclusion and exclusion criteria are met.

Patients will be enrolled at the first screening visit. Informed consent will be signed by both parents is required during enrollment. Informed assent will be offered for patients 14 years old and older. Eligible patients, ambulatory UC patients, requiring IFX for corticosteroid dependent or refractory moderate to severe disease (excluding acute severe UC), meeting inclusion/exclusion criteria, after obtaining informed consent, will be randomized (1:1 ratio in blocks of four, stratified by immunomodulators use) at enrollment visit (week 0, prior to IFX initiation) to either group 1 or group 2 using opaque, numbered and sealed envelopes. Prior corticosteroid treatment is allowed as a taper-down schedule during induction with IFX and must be terminated by week 10 (otherwise will be defined as induction failure). At each visit all patients will be examined and have height, weight, and PUCAI performed as well as comprehensive laboratory examinations including CBC, albumin, AST, ALT, ESR and CRP (CRP will be measured and registered in mg/dL) and fecal samples (4 grams) for bile acids and microbiome/virome. Fecal sample for fecal calprotectin (FC) will be obtained as well at weeks 20 and 52. Extent of disease will be registered using the Paris classification (Levine A et al, IBD, June 2011) and will be based on the latest colonoscopic evaluation (described only by macroscopic involvement). Patients who undergo a colonoscopy at any time as standard of care before initiating biologic therapy should register the results of colonoscopy (according to the Mayo score- A score of ≤1 is considered complete mucosal healing). In addition, every colonoscopy that will be performed during the study period based on physician discretion, should be register in the CRF (Colonoscopy is not part of this specific protocol).

The study period is composed of two distinctive phases: Intervention phase: week 0-20 and follow-up phase: week 21-52.

Group 1 (intervention group): Patients in group 1 will receive an accelerated induction at 0,1,3 weeks (5 mg/kg) and then at week 7,11,15.

Group 2 (control group): Patients in group 2 will receive a per protocol induction at 0,2,6 weeks (5 mg/kg) and then at week 14.

Intensification by shortening intervals between infusion rather than dose increment was chosen based on the pharmacokinetics of IFX in severe disease favoring this strategy in-order to maintain adequate trough drug-levels and avoid intermittent exposure (23).

Drug levels will be obtained prior to each infusion in each group in the intervention phase. Further maintenance will be planned according to drug levels at weeks 15 and 14, respectively. A visit concluding the intervention phase will be performed at week 20. The follow-up phase will continue without further interventions till week 52. During the follow-up phase (maintenance) treatment will be administered according to the treating physician discretion, with no restrictions.

Patients with induction failure in the control arm (defined as a lack of improvement of at least 20 points from the baseline PUCAI score OR PUCAI≥35 at 3 weeks following induction) will be able to undergo treatment intensification by decreasing infusion intervals according to the treating physician discretion.

Conditions

Ulcerative Colitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Accelerated induction

Patients in group 1 will receive an accelerated induction of infliximab at 0,1,3 weeks (5 mg/kg) and then at week 7,11,15.

Group Type: EXPERIMENTAL

Infliximab

Intervention Type: DRUG

Accelerated induction of infliximab in moderate to severe ambulatory prdiatric UC patients

Per protocol

Patients in group 2 will receive a per protocol induction of infliximab at 0,2,6 weeks (5 mg/kg) and then at week 14.

Group Type: ACTIVE_COMPARATOR

Infliximab

Intervention Type: DRUG

Accelerated induction of infliximab in moderate to severe ambulatory prdiatric UC patients

Interventions

Infliximab

Accelerated induction of infliximab in moderate to severe ambulatory prdiatric UC patients

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Ulcerative colitis

2. PUCAI≥35

3. Age: 6 - 17 years (inclusive)

4. Planned to initiate IFX therapy.

5. Naïve to biologics

6. Informed consent

7. Neg. PPD-Test, negative HBV- S Ag

8. Negative stool culture, parasites and clostridium toxin

Exclusion Criteria

1. Pregnancy.

2. Acute severe colitis.

3. Renal Failure.

4. Toxic megacolon.

5. Patients whose disease is confined to the rectum (i.e. proctitis).

6. Prior treatment with infliximab or adalimumab.

7. Previous malignancy.

8. Sepsis or active bacterial infection.

9. Known immune deficiency.

10. Positive Hepatitis B surface antigen or evidence for TB.

11. IBD unclassified.

• Minimum Eligible Age: 6 Years
• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Schneider Children's Medical Center, Israel

OTHER

Sponsor Role: lead

Responsible Party

Amit Assa

Head of IBD program

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Amit Assa, MD

Role: PRINCIPAL_INVESTIGATOR

Schneider Children's Medical Center, Israel

Locations

Schenider Children's Medical Center

Petah Tikva, , Israel

Countries

Israel

Other Identifiers

INDUCE

Identifier Type: -

Identifier Source: org_study_id