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Off Label Use of Infliximab in Adult Patients With Severe Eosinophilic Esophagitis (IEE)

Primary Purpose

Esophagitis

Status
Completed
Phase
Phase 2
Locations
Switzerland
Study Type
Interventional
Intervention
Infliximab
Sponsored by
Swiss EE Study Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Esophagitis focused on measuring Eosinophilic Esophagitis, TNF-alpha, TNF-alpha Blockade, Infliximab

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patients with severe, corticosteroid-dependent eosinophilic esophagitis

Exclusion Criteria:

  • Pregnancy
  • Evidence of latent or active tuberculosis
  • Other contra-indications for TNF-alpha blockers
  • Unstable medical conditions
  • Malignancies

Sites / Locations

  • EE-Clinics, Praxis Roemerhof

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1 (open-label)

Arm Description

prospective, open label, uncontrolled trial

Outcomes

Primary Outcome Measures

Tissue eosinophilia before and after therapy

Secondary Outcome Measures

Full Information

First Posted
August 30, 2007
Last Updated
April 6, 2009
Sponsor
Swiss EE Study Group
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1. Study Identification

Unique Protocol Identification Number
NCT00523354
Brief Title
Off Label Use of Infliximab in Adult Patients With Severe Eosinophilic Esophagitis
Acronym
IEE
Official Title
Phase 2 Proof-of-Concept Study to Analyze the Efficacy of in TNF-Alpha Blockade in Adult Patients With Severe, Corticosteroid-Dependent Eosinophilic Esophagitis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2009
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
September 2007 (Actual)
Study Completion Date
October 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Swiss EE Study Group

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Eosinophilic Esophagitis (EE) is a chronic inflammatory disorder of the esophagus with a constantly increasing prevalence. It has been demonstrated that the expression of the cytokine TNF-α is up regulated in EE and that this pro-inflammatory cytokine is highly expressed by the keratinocytes of the esophageal epithelium in patients with active EE. Furthermore, it has been shown that TNF-α is capable to induce eotaxin-3 production in keratinocytes. These results suggest that TNF-α plays a crucial role in the pathogenesis of EE. Based on these findings, the investigators plan a prospective T1 translational study with the purpose to evaluate the efficacy of an Infliximab monotherapy in adult patients with severe, corticosteroid-dependent EE.
Detailed Description
Study Principle: An open-conducted, un-controlled, off label use of Infliximab will be performed in at least 3 individuals with Eosinophilic Esophagitis (EE) to evaluate the efficacy of an TNF-α blockade in the treatment of adult patients with severe, isolated EE. Rationale for this Trial: Eosinophilic Esophagitis is a chronic, TH2-type dominant inflammatory disorder of the esophagus with a constantly increasing prevalence. It has been demonstrated that the cytokines TNF-α and IL-5 as well as the chemokine eotaxin-3 play a crucial role in the immuno-pathogenesis of this disease. These mediators are potential targets for therapeutic interventions. The established diagnostic criteria of EE are PPI-resistent esophageal related symptoms in combination with an infiltration of the esophageal mucosa with more than 20 eosinophils/hpf, a tissue where eosinophils are not normally encountered. Treatment strategies in chronic inflammations have basically two goals: 1) Relief of symptoms; and 2) Prevention of long-term damage of the affected organ, due to a persistence of an uncontrolled inflammation. Standard recommendations for medical therapy of EE include systemic or topical corticosteroids and leukotriene antagonists. The treatment with corticosteroids is limited by the occurence of steroid-dependence and steroid-resistance, as well as the corticosteroid adherent side effects. Infliximab, a chimeric monoclonal IgG antibody, is a potent inhibitor of the soluble and the membrane-bound form of TNF-α. Its efficacy in inducing and maintaining a remission in several TH1- and TH2-type inflammations is well documented. Infliximab is since more than 5 years approved for the therapy of these immune-mediated inflammations. Today, it is used as standard therapy in a subset of severe forms in these disorders. Meanwhile an overwhelming mass of data has confirmed the efficacy and the safety of this compound. Purpose of this Study:The purpose of this pilot-trial is to evaluate the efficacy of a TNF-α blockade with Infliximab monotherapy as induction-treatment in adult patients with severe EE.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophagitis
Keywords
Eosinophilic Esophagitis, TNF-alpha, TNF-alpha Blockade, Infliximab

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A

8. Arms, Groups, and Interventions

Arm Title
1 (open-label)
Arm Type
Experimental
Arm Description
prospective, open label, uncontrolled trial
Intervention Type
Drug
Intervention Name(s)
Infliximab
Other Intervention Name(s)
Remicade
Intervention Description
Induction therapy with 2 infusions, each 5 mg/kg body weight within 2 wks
Primary Outcome Measure Information:
Title
Tissue eosinophilia before and after therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients with severe, corticosteroid-dependent eosinophilic esophagitis Exclusion Criteria: Pregnancy Evidence of latent or active tuberculosis Other contra-indications for TNF-alpha blockers Unstable medical conditions Malignancies
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hans-Uwe Simon, MD and PhD
Organizational Affiliation
Deaprtment of Pharmacology, University Bern, Bern, Switzerland
Official's Role
Study Chair
Facility Information:
Facility Name
EE-Clinics, Praxis Roemerhof
City
Olten
State/Province
SO
ZIP/Postal Code
4600
Country
Switzerland

12. IPD Sharing Statement

Learn more about this trial

Off Label Use of Infliximab in Adult Patients With Severe Eosinophilic Esophagitis

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