Efficacy and Safety of Two Regimens of Maintenance Therapy in Children With Crohn Disease

NCT ID: NCT01559142

Last Updated: 2012-04-04

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE3
• Total Enrollment: 100 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-11-30
• Study Completion Date: 2012-12-31

Brief Summary

The aim of the study is confirmation of efficacy of induction therapy with three doses of infliximab In patients with Crohn disease aged 7-17 years, and comparison of efficacy and safety of two regiment of maintenance therapy:

1. Infliximab with immunomodulation

2. Infliximab alone

Detailed Description

Study project Screening (Days -14 do 0): Laboratory and endoscopic (up to three months before Day 0) results will be obtained to check with inclusion/exclusion criteria.

Part A (Days 1 to 71): Induction therapy with 3 doses of infliximab 5 mg/kg will be applied on days 1 - 15 - 43. Simultaneously in patients receiving steroids, steroid tapering will be performed up to 71 Day. At Day 71 clinical (PCDAI) and endoscopic assessment will be done. Patients with no clinical response will be qualified to Follow-up surveillance group. Patients with clinical response present will be randomized to two groups of maintenance therapy:

1. Infliximab with immunomodulation 2. Infliximab alone

Part B (Weeks 10 - 54): Patient with both groups will have scheduled visits at Weeks 14, 22, 30, 38, 46. Infliximab infusions and laboratory tests will be performed at each visit. At Week 54 clinical (PCDAI) and endoscopic assessment will be done.

Follow Up: 4 weeks after last visit - SAE monitoring Aim of the study

The aim of the study is confirmation of efficacy of induction therapy with three doses of infliximab In patients with Crohn disease aged 7-17 years, and comparison of efficacy and safety of two regiment of maintenance therapy:

1. Infliximab with immunomodulation

2. Infliximab alone Drug dosing in therapy regimens.

Infliximab: 5 mg/kg mc In intravenous infusion lasting over 2 hrs. Azathioprine: 1,5 - 3 mg/kg/24h Methotrexate: 10 - 25 mg/week

Safety assessment

AE and SAE monitoring will be conducted during whole period of the study

Efficacy assessment

Primary endpoint

Part A:

• Clinical response defined as: Decrease of PCDAI ≥ 15 points AND PCDAI less than 30 points

• Remission defined as: PCDAI ≤ 10 points

Part B:

• Loss of clinical response defined as:

Increase of PCDAI more than 15 points OR PCDAI > 30 points

Secondary endpoints

Part A:

• Time to steroid cessation

Part B:

• Necessity to increase/change maintenance therapy with

o Surgery

o Increase of infliximab dose

• Increase of immunomodulator dose
• Steroids induction

Statistical methods

• ITT analysis
• Primary endpoints: chi2 tests, Kaplan-Meier analysis
• Secondary endpoints: chi2 tests, Kaplan-Meier analysis, U Mann-Whitney analysis

Conditions

Crohn Disease

Study Design

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

Study Groups

IFX TG

Group Type: ACTIVE_COMPARATOR

Infliximab with azathioprine (IIFX + AZA)

Intervention Type: DRUG

Infliximab with azathioprine during whole one year study

IFX alone

Group Type: ACTIVE_COMPARATOR

Infliximab (IFX alone)

Intervention Type: DRUG

Infliximab continuously; azathioprine stopped in 26 week

Interventions

Infliximab with azathioprine (IIFX + AZA)

Infliximab with azathioprine during whole one year study

Intervention Type: DRUG

Infliximab (IFX alone)

Infliximab continuously; azathioprine stopped in 26 week

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patients with severe Crohn disease (PCDAI in anamnesis more than 51 points), with PCDAI currently over 30 points, with no or loss of response for previous therapy (except biological agents). Patients may have active fistulas.

2. Efficient methods of contraception in patients of childbearing potential during study period and six months after.

3. Patients will be enrolled to Part B of the study whether they finish Part A with clinical remission or clinical response.

Exclusion Criteria

1. Hypersensitivity to infliximab

2. Pregnancy and breastfeeding

3. Active tuberculosis or other severe infection: sepsis, opportunistic infections, active CMV, yersinia pseudotuberculosis, pneumocystis carini, atypical mycobacteriosis

4. VZV infection, hepatitis, pneumonia during 3 months before Day 0 of the study

5. pancytopaenia and aplastic anemia

6. moderate and severe heart insufficiency (NYHA class III/IV), or unstable coronary heart disease

7. chronic pulmonary insufficiency, chronic renal insufficiency, chronic liver insufficiency

8. HIV infection

9. Presence of severe diseases of nervous system or severe endocrinological, hematological, psychiatric diseases.

10. Demyelinisation syndrome or symptoms resembling Demyelinisation syndrome

11. Malignancy or premalignant conditions during 5 years before Day 0 of the study.

12. Severe infection currently present

13. Malignancy currently present

• Minimum Eligible Age: 7 Years
• Maximum Eligible Age: 17 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Children's Memorial Health Institute, Poland

OTHER

Sponsor Role: lead

Responsible Party

JAROSLAW KIERKUS

MD, PhD

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jaroslaw Kierkus, MD PhD

Role: PRINCIPAL_INVESTIGATOR

The Children's Memorial Institute

Locations

Department of Gastroenterology, Hepatology and Feeding Disorders

Warsaw, , Poland

Countries

Poland

Other Identifiers

IP CZD 2008-01-14

Identifier Type: -

Identifier Source: org_study_id