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CompletedNCT00523354IEEUpdated Apr 7, 2009

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

A Phase 2 interventional study of Infliximab in Esophagitis, sponsored by Swiss EE Study Group. Completed at 1 site in Switzerland. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2009-04-07.

Sponsored by Swiss EE Study Group · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Esophagitis

Keywords

  • Eosinophilic Esophagitis
  • TNF-alpha
  • TNF-alpha Blockade
  • Infliximab
03

In context

Esophagitis

322 studies on the registry are indexed under Esophagitis; 37 are open to participants now.

Browse Esophagitis studies →

Lead sponsor

Swiss EE Study Group is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adult patients with severe, corticosteroid-dependent eosinophilic esophagitis

Exclusion criteria

Exclusion Criteria:

  • Pregnancy
  • Evidence of latent or active tuberculosis
  • Other contra-indications for TNF-alpha blockers
  • Unstable medical conditions
  • Malignancies
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)

Study arms

  • Experimental
    1 (open-label)

    prospective, open label, uncontrolled trial

    Drug: Infliximab

Interventions

  • DrugInfliximab

    Induction therapy with 2 infusions, each 5 mg/kg body weight within 2 wks

    Also known as: Remicade

06

What researchers measure

Primary outcomes

  1. Tissue eosinophilia before and after therapy

07

Study locations

1 site
  • EE-Clinics, Praxis Roemerhof
    Olten, SO 4600, Switzerland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 7, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00523354
Lead sponsor
Swiss EE Study Group
First posted
Aug 31, 2007
Start date
Aug 2007
Primary completion
Sep 2007
Completion
Oct 2007
Last update
Apr 7, 2009

Study contacts

Hans-Uwe Simon, MD and PhD
study chair · Deaprtment of Pharmacology, University Bern, Bern, Switzerland

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2009. You cannot join it, but the record below documents what was studied.

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