- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01705795
Anti-IL-5 Therapy in Bullous Pemphigoid (BP)
Anti-IL-5 Therapy in Bullous Pemphigoid. Randomized, Placebo-controlled, Double-blind Study Evaluating the Effect of Anti-IL-5 Therapy in Patients With Bullous Pemphigoid.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background
Bullous pemphigoid (BP) is the most common autoimmune blistering skin disease. It characteristically affects the elderly (>70 years) with an annual incidence of 5 to 35 per million. This is comparable with the incidence of eosinophilic esophagitis that we determined with approximately 14 per million. Eosinophilic esophagitis has been recognized as an emerging medical problem and, consequently, several studies with anti-IL-5-antibodies have been performed and are still ongoing. It should be noted, however, that, in contrast to eosinophilic esophagitis, the incidence of BP is dramatically increasing with an average of 17% per year. Moreover, with the increase of the proportion of the elderly in the industrialized world, the medical problems associated with BP will even be more visible in the near future. For instance, patients with BP have an increased mortality risk of 2.3. In the US, an increase in mortality of BP patients has been noticed from 1979 to 2002. Taken together, BP is a frequent disease that affects mostly the elderly.
BP often starts with extremely pruritic skin lesions resembling eczema or urticaria before vesicles and blisters arise. In 10-30% of patients, BP also involves the oral mucosa. Disease severity can be determined by means of the autoimmune bullous skin disorder intensity score (ABSIS) that evaluates the involved area as well as the disease activity. The disease is due to an autoimmune response to structural components of junctional adhesion complexes leading to the damage of the dermal-epidermal junction with subepidermal blister formation. Specifically, autoreactive B and T cell responses against the hemidesmosomal antigens BP180 and BP230 have been identified. Serum levels of autoantibodies to BP180 reflect the disease severity and activity. The T cells are memory CD4+ cells producing both Th1 and Th2 cytokines, mostly IL-4, IL-5 and IL-13. IL-5 as well as eotaxin are abundantly found in blister fluids. The production of IL-5 is indeed associated with blood eosinophilia and significant eosinophil infiltration in the skin of BP patients. Eosinophils are thought to be critically implicated in blister formation by releasing toxic granule proteins (ESP, MBP) and proteolytic enzymes.
Systemic corticosteroids have been widely used for the treatment of BP. Nevertheless, the use of steroids is limited by their side effects. in therapy-resistant cases, immunosuppressive drugs such as azathioprine, chlorambucil, cyclophosphamide, cyclosporine, methotrexate, mycophenolate mofetil are employed, but their corticosteroid-sparing effect and overall benefit in BP is highly disputed. 70% of the relapses are usually observed within three months, 85% within 6 months after stopping therapy.
Since eosinophils are characteristically found in the skin at early stages of the disease before blisters occur and contribute to tissue damage, targeting eosinophils by reducing their number and activation might thus be a promising alternative therapeutic approach. Anti-IL-5 antibody therapy has been shown to be effective in depleting eosinophils, e.g. in diseases such as eosinophilic esophagitis and hypereosinophilic syndrome.
Objective
To determine the safety and efficacy of mepolizumab in patients with bullous pemphigoid.
Methods
clinical trial with 750 mg mepolizumab over three months, evaluate time period from start of therapy until relapse, ABSIS-Score, Pruritus Score, Antibody levels, immuno pathological evaluation of skin biopsy.
Study Type
Enrollment (Actual)
Phase
- Phase 2
Contacts and Locations
Study Locations
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-
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Bern, Switzerland, 3010
- Dep. of Dermatology, Bern University Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Men, women >18 years
- Active BP (diagnosed by typical clinical picture and skin biopsy)
- Must give written informed consent
Exclusion Criteria
- Patients with other skin disease
- Patients with severe diseases of other organ systems
- Systemic treatment for BP
- Topical therapy with corticosteroids and other anti-inflammatory substances
- For female patients, unless postmenopausal or surgically sterile, unwillingness to practice effective contraception (defined as methods with <1% failure rate)
- Female patients who are currently pregnant or breast-feeding
- Current abuse of alcohol and/or drugs
- History of or a new diagnosis or treatment of an invasive malignancy within 5 years of enrollment. Patients with a history of treated squamous cell and/or basal cell carcinomas limited to the skin are not excluded.
- History of recurrent clinically significant infection
- Congenital or acquired immunodeficiency syndrome
- Current enrollment in any other investigational drug study
- Previous participation in this study or previous studies with mepolizumab
- Hypersensitivity to mepolizumab or its constituents
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
ACTIVE_COMPARATOR: Mepolizumab
Mepolizumab 750 mg four times one month apart.
|
750mg mepolizumab four times over four months
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PLACEBO_COMPARATOR: Placebo
Placebo (saline) four times one month apart
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Nacl four times over four months
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Time period (in days) from start of therapy until relapse, mepolizumab vs placebo
Time Frame: Before, at 3-9 months
|
Before, at 3-9 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Changes of BP severity score over time (ABSIS)
Time Frame: At baseline, during therapy (expected to be ca. 4 months), follow up (expected to be ca. 9 months)
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At baseline, during therapy (expected to be ca. 4 months), follow up (expected to be ca. 9 months)
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Changes of pruritus score (visual analog scale)
Time Frame: At baseline, during therapy (expected to be ca. 4 months), follow up (expected to be ca. 9 months)
|
At baseline, during therapy (expected to be ca. 4 months), follow up (expected to be ca. 9 months)
|
Changes of BP-antibody titers over time
Time Frame: At baseline, during therapy (expected to be ca. 4 months), follow up (expected to be ca. 9 months)
|
At baseline, during therapy (expected to be ca. 4 months), follow up (expected to be ca. 9 months)
|
Number of patients with AE, severity of AE
Time Frame: At baseline, during therapy (expected to be ca. 4 months), follow up (expected to be ca. 9 months)
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At baseline, during therapy (expected to be ca. 4 months), follow up (expected to be ca. 9 months)
|
Collaborators and Investigators
Investigators
- Principal Investigator: Dagmar Simon, Inselspital, Bern University Hospital
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 191/11
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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