Top-down Infliximab Study in Kids With Crohn's Disease (TISKids)
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ClinicalTrials.gov Identifier: NCT02517684 |
Recruitment Status :
Active, not recruiting
First Posted : August 7, 2015
Last Update Posted : February 16, 2023
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Condition or disease | Intervention/treatment | Phase |
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Crohn's Disease | Drug: Infliximab Drug: Prednisolone Other: Exclusive enteral nutrition Drug: Azathioprine | Phase 4 |
Objective: The purpose of this study is to determine whether a top-down treatment approach, prescribing IFX and AZA at diagnose, yields better outcome in comparison to the usual step-up treatment approach, starting with prednison and AZA or EEN and AZA, in moderate-to-severe pediatric CD patients.
Sample size: We will include 100 (2 x 50) patients. With these numbers a difference of 60% and 85% (= 25) can be shown at a power of 80% (2-sided α 0.05).
Study design: an international open-label randomised controlled trial Study population: Children (age 3-17 yrs) with new-onset, untreated, CD with moderate-to-severe disease activity (weighted Pediatric CD Index [wPCDAI] >40) Intervention: Patients will be randomised to either top-down or conventional step-up treatment.
Treatment arm 1: Top-down IFX treatment will consist of a total of 5 IFX infusions of 5 mg/kg (IFX induction at week 0, 2 and 6, followed by 2 maintenance infusions every 8 weeks) combined with oral AZA 2-3 mg/kg once daily. AZA therapy will continue after the last IFX infusion to maintain remission.
Treatment arm 2: Step-up treatment will consist of standard induction treatment by either oral prednisolone 1 mg/kg (maximum 40 mg) once daily for 4 weeks, followed by tapering in 6 weeks until stop, or EEN with polymeric feeding for 6-8 weeks after which normal foods are gradually reintroduced within 2-3 weeks. Either of these induction treatments will be combined with oral AZA 2-3 mg, once daily, as maintenance treatment.
Main study parameters/endpoints: Clinical remission at 52 weeks without need for additional CD related therapy or surgery. Secondary endpoints include clinical response, remission and mucosal healing at week 10 and 52, growth, quality of life and adverse events.
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 100 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Top-down Infliximab Study in Kids With Crohn's Disease |
Actual Study Start Date : | April 2015 |
Actual Primary Completion Date : | December 2019 |
Estimated Study Completion Date : | December 2023 |

Arm | Intervention/treatment |
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Experimental: Top-down
Infliximab and azathioprine; patients will receive 5 infliximab infusions of 5 mg/kg (IFX induction at week 0, 2 and 6, followed by 2 maintenance infusions every 8 weeks). IFX will be discontinued after 5 IFX infusions. Patients will also receive oral azathioprine 2-3 mg/kg, once daily as maintenance treatment.
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Drug: Infliximab
Other Name: Inflectra Drug: Azathioprine Other Name: Imuran |
Active Comparator: Step-up
Step-up treatment will consist of standard induction treatment by either oral prednisolone 1 mg/kg (maximum 40 mg) once daily for 4 weeks, followed by tapering in 6 weeks until stop, or EEN with polymeric feeding for 6-8 weeks after which normal foods are gradually reintroduced within 2-3 weeks. Either of these induction treatments will be combined with oral AZA 2-3 mg, once daily, as maintenance treatment.
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Drug: Prednisolone Other: Exclusive enteral nutrition Drug: Azathioprine Other Name: Imuran |
- Clinical remission without need for additional CD related therapy or surgery [ Time Frame: 52 weeks ]Clinical remission is defined as a weighted Pediatric Crohn's Disease Activity Index (wPCDAI) score of less than 12.5 points
- Clinical response rates [ Time Frame: 10 weeks ]Response is defined by a decrease in wPCDAI score above 17.5 points compared to baseline
- Clinical remission rates [ Time Frame: 10 and 52 weeks ]Remission is wPCDAI<12.5
- Mucosal healing [ Time Frame: 10 and 52 weeks ]Assessed by endoscopy (SES-CD) and/or fecal calprotectin (<100microgram/gram)
- Change in height Z-scores [ Time Frame: 10 and 52 weeks ]
- Change in BMI Z-scores [ Time Frame: 10 and 52 weeks ]
- Change bone age [ Time Frame: 10 and 52 weeks ]
- Change in Tanner stage [ Time Frame: 10 and 52 weeks ]
- Therapy failure rates over time [ Time Frame: 52 weeks ]Therapy failure: primary non-response, loss of response according to wPCDAI and medication intolerance
- Adverse events rates [ Time Frame: 52 weeks, and 260 weeks ]Adverse events includes therapy side effects, disease complications (fistulas, abscesses, strictures, surgery, extra-intestinal manifestations)
- Cumulative therapy use [ Time Frame: 52 weeks, and 260 weeks ]
- Long-term yearly remission rates without need for additional CD related therapy or surgery [ Time Frame: 260 weeks ]Clinical remission is defined as a weighted Pediatric Crohn's Disease Activity Index (wPCDAI) score of less than 12.5 points
- Long-term yearly number of flares [ Time Frame: 260 weeks ]
- Long-term yearly clinical remission rates [ Time Frame: 260 weeks ]Clinical remission is defined as a weighted Pediatric Crohn's Disease Activity Index (wPCDAI) score of less than 12.5 points
- Long-term yearly mucosal healing (calprotectin) rates [ Time Frame: 260 weeks ]fecal calprotectin <100microgram/gram

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Ages Eligible for Study: | 3 Years to 17 Years (Child) |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Children (age 3-17 years, both male and female, weight >10kg) with new-onset,
- untreated CD with moderate-to-severe disease activity assessed by a wPCDAI >40 will be eligible for inclusion after a diagnosis of CD was made based on the Porto criteria
Exclusion Criteria:
Patients with the following characteristics will be excluded:
- immediate need for surgery,
- symptomatic stenosis or stricture in the bowel due to scarring,
- active perianal fistulas,
- severe co-morbidity,
- severe infection such as sepsis or opportunistic infections,
- positive stool culture,
- positive Clostridium difficile assay,
- positive tuberculin test or a chest radiograph consistent with tuberculosis or malignancy,
- those already started with CD specific therapy,
- patients with a suspected or
- definitive pregnancy

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02517684
Belgium | |
University Hospital Brussels | |
Brussels, Belgium | |
University Hospitals Leuven | |
Leuven, Belgium | |
Finland | |
Helsinki University Central Hospital | |
Helsinki, Finland | |
Netherlands | |
Erasmus Medical Center | |
Rotterdam, Zuid-Holland, Netherlands, 3000 CA | |
Academic Medical Center | |
Amsterdam, Netherlands | |
VU University Medical Center | |
Amsterdam, Netherlands | |
Amphia Hospital | |
Breda, Netherlands | |
Medisch Spectrum Twente | |
Enschede, Netherlands | |
Leiden University Medical Center | |
Leiden, Netherlands | |
Radboud University Medical Center | |
Nijmegen, Netherlands | |
Maasstad Hospital | |
Rotterdam, Netherlands | |
University Medical Center Utrecht | |
Utrecht, Netherlands | |
Isala hospital | |
Zwolle, Netherlands |
Principal Investigator: | Lissy de Ridder, MD PhD | Erasmus Medical Center |
Responsible Party: | Lissy de Ridder, Pediatric Gastroenterologist, Erasmus Medical Center |
ClinicalTrials.gov Identifier: | NCT02517684 |
Other Study ID Numbers: |
NL52030.078.15 2014-005702-37 ( EudraCT Number ) MEC-2015-080 ( Other Identifier: Medical Ethical Trial Committee Erasmus MC ) |
First Posted: | August 7, 2015 Key Record Dates |
Last Update Posted: | February 16, 2023 |
Last Verified: | February 2023 |
Crohn's disease pediatric infliximab top-down TISKids |
Crohn Disease Inflammatory Bowel Diseases Gastroenteritis Gastrointestinal Diseases Digestive System Diseases Intestinal Diseases Prednisolone Infliximab Azathioprine Anti-Inflammatory Agents Glucocorticoids Hormones Hormones, Hormone Substitutes, and Hormone Antagonists |
Physiological Effects of Drugs Antineoplastic Agents, Hormonal Antineoplastic Agents Gastrointestinal Agents Tumor Necrosis Factor Inhibitors Dermatologic Agents Antirheumatic Agents Antimetabolites Molecular Mechanisms of Pharmacological Action Antimetabolites, Antineoplastic Immunosuppressive Agents Immunologic Factors |