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Thalidomide Versus Infliximab in New Onset Crohn's Disease With Poor Prognostic Factors

Primary Purpose

Crohn Disease

Status
Terminated
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Thalidomide
Infliximab
Sponsored by
IRCCS Burlo Garofolo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn Disease focused on measuring Children, Crohn disease, Thalidomide, Mucosal healing

Eligibility Criteria

6 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age at diagnosis <18 years and >=6 years
  • New diagnosis of CD based on Porto criteria
  • CD with inflammatory phenotype (non-penetrating, non-fistulizing) and with no need for surgery except for perinal fistulas
  • Presence of at least one of the following risk factors for poor prognosis:

    • fistulizing perianal disease
    • pan-enteric disease
    • disease extension > 60 cm
    • severe growth delay (height z-score < -2 DS)
    • severe osteoporosis (z score < -2 DS)
    • hypoalbuminemia (< 3g/dL) or high C-reactive protein (2 times higher the normal range)
  • Acceptance of the Risk Evaluation and Mitigation Strategy (REMS) program for reducing the teratogenic risk.

Exclusion Criteria:

  • ongoing pregnancy
  • presence of peripheral neuropathy
  • HIV
  • patients with transplanted organs
  • ongoing major infections or other severe diseases
  • participation to other experimental studies.

Sites / Locations

  • Dipartimento di Pediatria dell'Università di Napoli "Federico II"
  • IRCCS Burlo Garofolo
  • Pediatria III Gastroenterologia ed Endoscopia Digestiva, Istituto Giannina Gaslini
  • Fondazione MBBM , Azienda Ospedaliera San Gerardo - Università Milano Bicocca
  • Unità di Gastroenterologia Pediatrica e Fibrosi Cistica, Dipartimento di Scienze Pediatriche Mediche e Chirurgiche, Policlinico Universitario
  • Gastroenterologia e Nutrizione Pediatrica, Azienda Ospedaliero Universitaria Meyer

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Thalidomide

Infliximab

Arm Description

Thalidomide is a immunomodulatory and antiangiogenetic drug with anti tumor necrosis factor (TNF) alpha properties

Infliximab is a chimeric monoclonal antibody against TNF alpha

Outcomes

Primary Outcome Measures

Efficacy in inducing mucosal healing
Proportion of patients that achieve mucosal healing, defined by a Simplified Endoscopic Activity Index for CD (SES-CD) ≤ 2.

Secondary Outcome Measures

Efficacy in inducing clinical response
Clinical response will be evaluated with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI), defined by a reduction of wPCDAI > 50% from the basal values.
Efficacy in inducing clinical response
Clinical response will be evaluated with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI), defined by a reduction of wPCDAI > 50% from the basal values.
Efficacy in inducing clinical remission
Clinical remission will be evaluated with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI), defined by a wPCDAI <12.5.
Efficacy in inducing clinical remission
Clinical remission will be evaluated with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI), defined by a wPCDAI <12.5.
Efficacy in reducing the need to change therapy
Evaluation of the proportion of patients that need a therapeutic change
Efficacy in reducing the need to change therapy
Evaluation of the proportion of patients that need a therapeutic change
Efficacy in reducing hospitalizations
Evaluation of the proportion of patients that need hospitalization.
Efficacy in reducing the need for surgery
Evaluation of the proportion of patients that need surgery
Efficacy in reducing erythrocyte sedimentation rate
Evaluation of the trend of erythrocyte sedimentation rate (ESR)
Efficacy in reducing C-reactive protein
Evaluation of the trend of C-reactive protein (CRP)
Efficacy in reducing faecal calprotectin
Evaluation of the trend of faecal calprotectin
Efficacy in modifying body mass index
Evaluation of the trend of body mass index, defined as weight (kg)/height (m)^2
Efficacy in modifying height-for-age z score
Evaluation of the trend of height-for-age z score
Efficacy in modifying weight-for-age z score
Evaluation of the trend of weight-for-age z score
Evaluation of the Treatment-Emergent Adverse Events
Number and type
Direct and indirect costs
Comparison of direct and indirect costs (i.e. drugs, medical supplies and equipment, laboratory and diagnostic tests, hospitalizations, visits, transportation to and from healthcare facilities, missing work and school days…) between the two groups

Full Information

First Posted
July 5, 2017
Last Updated
September 2, 2020
Sponsor
IRCCS Burlo Garofolo
Collaborators
Centro di Riferimento Oncologico - Aviano, Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
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1. Study Identification

Unique Protocol Identification Number
NCT03221166
Brief Title
Thalidomide Versus Infliximab in New Onset Crohn's Disease With Poor Prognostic Factors
Official Title
Thalidomide, a Novel Immunological Treatment to Modify the Natural History of Paediatric Crohn's Disease: a New Proposal From a Well-established Paediatric Research Network
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Terminated
Why Stopped
Difficulty in recruiting subjects who meet the inclusion/exclusion criteria
Study Start Date
February 27, 2018 (Actual)
Primary Completion Date
July 31, 2020 (Actual)
Study Completion Date
July 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
IRCCS Burlo Garofolo
Collaborators
Centro di Riferimento Oncologico - Aviano, Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

4. Oversight

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

5. Study Description

Brief Summary
Crohn's disease (CD) is a life-long inflammatory bowel disease disease with an unknown pathogenesis. The ultimate goal of therapy is to modify the natural history of CD thus reducing complications. Thalidomide is a small molecule with immunomodulatory and anti-angiogenetic properties. It is currently approved for the treatment of erythema nodosum leprosum, an immunological complication of leprosy and multiple myeloma. It has also been used in several other inflammatory diseases of the skin and of the mucosal membranes, such as Behcet disease, oropharyngeal ulcers in AIDS, cutaneous lupus, and graft versus host disease. Many case series and one pediatric randomized controlled trial proved the efficacy of thalidomide in the treatment of children with CD refractory to standard treatments. In these patients, clinical remission was achieved in about 50% of the cases and was maintained for a mean time superior of 3 years. Mucosal healing after 52 weeks of treatment was observed in 40% of the patients in clinical remission. Moreover, thalidomide was found to have a steroid-sparing effect and to decrease the need for surgical interventions. The clinical and endoscopic efficacy of thalidomide was also observed in children with failure to respond or intolerance to anti-TNF biological drugs. The aim of this multicentric prospective randomized controlled is to evaluate the efficacy and safety of thalidomide vs infliximab in changing the natural history of CD in patients with poor prognostic outcome. Moreover, the study will evaluate the immunological and genetical mechanisms of CD, the mechanisms of action thalidomide in CD and will the pharmacokinetics, metabolomics and pharmacogenomics of thalidomide, and their impact on thalidomide safety and effectiveness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn Disease
Keywords
Children, Crohn disease, Thalidomide, Mucosal healing

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Thalidomide
Arm Type
Experimental
Arm Description
Thalidomide is a immunomodulatory and antiangiogenetic drug with anti tumor necrosis factor (TNF) alpha properties
Arm Title
Infliximab
Arm Type
Active Comparator
Arm Description
Infliximab is a chimeric monoclonal antibody against TNF alpha
Intervention Type
Drug
Intervention Name(s)
Thalidomide
Intervention Description
Thalidomide is a immunomodulatory and antiangiogenetic drug with anti TNF alpha properties
Intervention Type
Drug
Intervention Name(s)
Infliximab
Intervention Description
Infliximab is a chimeric monoclonal antibody against TNF alpha
Primary Outcome Measure Information:
Title
Efficacy in inducing mucosal healing
Description
Proportion of patients that achieve mucosal healing, defined by a Simplified Endoscopic Activity Index for CD (SES-CD) ≤ 2.
Time Frame
52 weeks
Secondary Outcome Measure Information:
Title
Efficacy in inducing clinical response
Description
Clinical response will be evaluated with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI), defined by a reduction of wPCDAI > 50% from the basal values.
Time Frame
12 weeks
Title
Efficacy in inducing clinical response
Description
Clinical response will be evaluated with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI), defined by a reduction of wPCDAI > 50% from the basal values.
Time Frame
52 weeks
Title
Efficacy in inducing clinical remission
Description
Clinical remission will be evaluated with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI), defined by a wPCDAI <12.5.
Time Frame
12 weeks
Title
Efficacy in inducing clinical remission
Description
Clinical remission will be evaluated with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI), defined by a wPCDAI <12.5.
Time Frame
52 weeks
Title
Efficacy in reducing the need to change therapy
Description
Evaluation of the proportion of patients that need a therapeutic change
Time Frame
12 weeks
Title
Efficacy in reducing the need to change therapy
Description
Evaluation of the proportion of patients that need a therapeutic change
Time Frame
52 weeks
Title
Efficacy in reducing hospitalizations
Description
Evaluation of the proportion of patients that need hospitalization.
Time Frame
52 weeks
Title
Efficacy in reducing the need for surgery
Description
Evaluation of the proportion of patients that need surgery
Time Frame
52 weeks
Title
Efficacy in reducing erythrocyte sedimentation rate
Description
Evaluation of the trend of erythrocyte sedimentation rate (ESR)
Time Frame
Each time point between enrolment and 52 weeks (0, 4, 8, 14, 26, 38, 52 weeks)
Title
Efficacy in reducing C-reactive protein
Description
Evaluation of the trend of C-reactive protein (CRP)
Time Frame
Each time point between enrolment and 52 weeks (0, 4, 8, 14, 26, 38, 52 weeks)
Title
Efficacy in reducing faecal calprotectin
Description
Evaluation of the trend of faecal calprotectin
Time Frame
Each time point between enrolment and 52 weeks (0, 4, 8, 14, 26, 38, 52 weeks)
Title
Efficacy in modifying body mass index
Description
Evaluation of the trend of body mass index, defined as weight (kg)/height (m)^2
Time Frame
Each time point between enrolment and 52 weeks (0, 4, 8, 14, 26, 38, 52 weeks)
Title
Efficacy in modifying height-for-age z score
Description
Evaluation of the trend of height-for-age z score
Time Frame
Each time point between enrolment and 52 weeks (0, 4, 8, 14, 26, 38, 52 weeks)
Title
Efficacy in modifying weight-for-age z score
Description
Evaluation of the trend of weight-for-age z score
Time Frame
Each time point between enrolment and 52 weeks (0, 4, 8, 14, 26, 38, 52 weeks)
Title
Evaluation of the Treatment-Emergent Adverse Events
Description
Number and type
Time Frame
Between enrolment and 52 weeks
Title
Direct and indirect costs
Description
Comparison of direct and indirect costs (i.e. drugs, medical supplies and equipment, laboratory and diagnostic tests, hospitalizations, visits, transportation to and from healthcare facilities, missing work and school days…) between the two groups
Time Frame
52 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age at diagnosis <18 years and >=6 years New diagnosis of CD based on Porto criteria CD with inflammatory phenotype (non-penetrating, non-fistulizing) and with no need for surgery except for perinal fistulas Presence of at least one of the following risk factors for poor prognosis: fistulizing perianal disease pan-enteric disease disease extension > 60 cm severe growth delay (height z-score < -2 DS) severe osteoporosis (z score < -2 DS) hypoalbuminemia (< 3g/dL) or high C-reactive protein (2 times higher the normal range) Acceptance of the Risk Evaluation and Mitigation Strategy (REMS) program for reducing the teratogenic risk. Exclusion Criteria: ongoing pregnancy presence of peripheral neuropathy HIV patients with transplanted organs ongoing major infections or other severe diseases participation to other experimental studies.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alessandro Ventura, MD PhD
Organizational Affiliation
IRCCS Burlo Garofolo
Official's Role
Study Chair
Facility Information:
Facility Name
Dipartimento di Pediatria dell'Università di Napoli "Federico II"
City
Napoli
State/Province
Campania
ZIP/Postal Code
80131
Country
Italy
Facility Name
IRCCS Burlo Garofolo
City
Trieste
State/Province
Friuli Venezia Giulia
ZIP/Postal Code
34137
Country
Italy
Facility Name
Pediatria III Gastroenterologia ed Endoscopia Digestiva, Istituto Giannina Gaslini
City
Genoa
State/Province
Liguria
ZIP/Postal Code
16147
Country
Italy
Facility Name
Fondazione MBBM , Azienda Ospedaliera San Gerardo - Università Milano Bicocca
City
Monza
State/Province
Lombardia
ZIP/Postal Code
20052
Country
Italy
Facility Name
Unità di Gastroenterologia Pediatrica e Fibrosi Cistica, Dipartimento di Scienze Pediatriche Mediche e Chirurgiche, Policlinico Universitario
City
Messina
State/Province
Sicilia
ZIP/Postal Code
98124
Country
Italy
Facility Name
Gastroenterologia e Nutrizione Pediatrica, Azienda Ospedaliero Universitaria Meyer
City
Firenze
State/Province
Toscana
ZIP/Postal Code
50139
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Thalidomide Versus Infliximab in New Onset Crohn's Disease With Poor Prognostic Factors

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