Immunoadsorption, Dexamethasone Pulse Therapy and Rituximab for Pemphigus
Primary Purpose
Pemphigus
Status
Completed
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
Combination of Protein A Immunoadsorption, Rituximab, Dexamethasone plus Azathioprine
Sponsored by
About this trial
This is an interventional treatment trial for Pemphigus focused on measuring pemphigus, rituximab, immunoadsorption, dexamethasone, treatment, management
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of pemphigus confirmed by immunofluorescence and desmoglein ELISA.
- Severe disease or past treatment(s) not effective or past treatment(s) not tolerated.
Exclusion Criteria:
- General condition too poor to tolerate immunoadsorption treatment.
- Severe dementia or psychiatric disease.
Sites / Locations
- Department of Dermatology, University of Luebeck
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Immunoadsorption/Dexamethasone/Rituximab
Arm Description
Outcomes
Primary Outcome Measures
Number of Patients Achieving a Short- and Long-term Remission of Pemphigus
Clinical remission was graded as partial remission on therapy, complete remission on therapy and complete remission off therapy, as described by Murell et al, J Am Acad Dermatol, 2008; 58:1043-6.
Secondary Outcome Measures
Number of Patients Who Experienced Side-effects of Treatment
Patients who experienced side-effects were counted. In addition, the nature and severity of side-effects were recorded.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00656656
Brief Title
Immunoadsorption, Dexamethasone Pulse Therapy and Rituximab for Pemphigus
Official Title
Combined Treatment of Autoimmune Bullous Diseases With Protein A Immunoadsorption, Dexamethasone Pulse Therapy and Rituximab
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Luebeck
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Pemphigus is a severe autoimmune blistering disease mediated by circulating antibodies against certain proteins important for maintaining skin integrity. Protein A immunoadsorption is a dialysis-like technique selectively removing the antibodies from patient's blood. Rituximab is a synthetic antibody capable of destroying B cells. B cells are responsible for production of antibodies in the patients blood that, in turn, lead to clinical signs of pemphigus. Dexamethasone pulse therapy is a high-dose short-term corticosteroid therapy that may be used to suppress autoantibody production in pemphigus. While each of these three therapies had been used to treat pemphigus, none was shown effective in all cases. The hypothesis of this study is that a combination of protein A immunoadsorption, rituximab and dexamethasone is more effective that either of these treatments alone in achieving a rapid and durable improvement or cure in patients with pemphigus.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pemphigus
Keywords
pemphigus, rituximab, immunoadsorption, dexamethasone, treatment, management
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
23 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Immunoadsorption/Dexamethasone/Rituximab
Arm Type
Other
Intervention Type
Drug
Intervention Name(s)
Combination of Protein A Immunoadsorption, Rituximab, Dexamethasone plus Azathioprine
Intervention Description
Protein A Immunoadsorption: performed on 3 consecutive days every 3 weeks
Rituximab: 1000 mg i.v. given twice at a 2-week interval
Dexamethasone pulse therapy: 100 mg i.v. given on 3 consecutive days every 3 weeks
Azathioprine: 2.5 mg/kg body weight daily p.o.
Primary Outcome Measure Information:
Title
Number of Patients Achieving a Short- and Long-term Remission of Pemphigus
Description
Clinical remission was graded as partial remission on therapy, complete remission on therapy and complete remission off therapy, as described by Murell et al, J Am Acad Dermatol, 2008; 58:1043-6.
Time Frame
up to 43 months
Secondary Outcome Measure Information:
Title
Number of Patients Who Experienced Side-effects of Treatment
Description
Patients who experienced side-effects were counted. In addition, the nature and severity of side-effects were recorded.
Time Frame
up to 43 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of pemphigus confirmed by immunofluorescence and desmoglein ELISA.
Severe disease or past treatment(s) not effective or past treatment(s) not tolerated.
Exclusion Criteria:
General condition too poor to tolerate immunoadsorption treatment.
Severe dementia or psychiatric disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Detlef Zillikens, MD
Organizational Affiliation
Department of Dermatology, University of Luebeck
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Dermatology, University of Luebeck
City
Luebeck
State/Province
Schleswig-Holstein
ZIP/Postal Code
23552
Country
Germany
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Immunoadsorption, Dexamethasone Pulse Therapy and Rituximab for Pemphigus
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