Comparison Between Rituximab Treatment and General Corticotherapy Treatment in Patients With Pemphigus (Rituximab 3)
Primary Purpose
Pemphigus Disease
Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
General Corticotherapy
Rituximab
Sponsored by
About this trial
This is an interventional treatment trial for Pemphigus Disease focused on measuring Corticothérapy, Rituximab, therapeutic efficacity, therapeutic tolerance
Eligibility Criteria
Inclusion Criteria:
- age >=18 and <= 80years
- consent obtained from patient
- effective female contraceptive method for women in procreate age
- new case of pemphigus vulgaris (PV) or pemphigus foliaceus (PF)
Exclusion Criteria:
- pemphigus vulgaris (PV) or pemphigus foliaceus (PF) treated
- pregnant woman or nursing mother
- woman able to have a baby and without contraception during the clinical trial period
- age < 18 or > 80
- karnovsky < 50%
- serious antecedents of allergy or anaphylactic reaction with human monoclonal antibody
- patient with depletion lymphocytic treatment in the next month
- unstable angina or ischemic heart disease
- cardiac insufficiency
- cardiac rhythm trouble uncontrolled
- positive HIV serology
- positive hepatitis B and / or C serology
- no consent
Sites / Locations
- CHU de Rouen - Hôpitaux de Rouen
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Rituximab
Corticotherapy
Arm Description
General Corticotherapy
Outcomes
Primary Outcome Measures
Number of patients with pemphigus controlled 24 months after the start of Rituximab treatment
Secondary Outcome Measures
Number of patients with pemphigus with both cutaneous and mucosal lesions healing after 6 months of rituximab treatment
Full Information
NCT ID
NCT00784589
First Posted
November 3, 2008
Last Updated
June 13, 2017
Sponsor
University Hospital, Rouen
1. Study Identification
Unique Protocol Identification Number
NCT00784589
Brief Title
Comparison Between Rituximab Treatment and General Corticotherapy Treatment in Patients With Pemphigus
Acronym
Rituximab 3
Official Title
Comparison Between Monoclonal Antibody CD20 Treatment (Rituximab (mabthéra))and General Corticotherapy Treatment in Patients With Pemphigus
Study Type
Interventional
2. Study Status
Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
July 2009 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Rouen
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Pemphigus is a severe and sometimes life-threatening disease with a mortality rate between 5 and 10 percent depending on the severity of disease and age of patients.
The standard of care is high doses of corticosteroids (CS) (usually, prednisone, 1 to 1.5. mg/kg/day, which are often associated with immunosuppressive drugs i.e., azathioprine, mycophenolate mofetil, cyclophosphamide, cyclosporine, although only one randomised study has demonstrated the superiority of the combination of corticosteroids and immunosuppressive drugs as compared to corticosteroids alone (9). Because of the low frequency of the disease, control trials are difficult to conduct. Evaluation of the different treatment regimens proposed, i;e; corticosteroids alone, CS and immunosuppressive drugs, IV immunoglobulins or new therapeutic regimens such as rituximab (an anti-CD20 monoclonal antibody directed against B- lymphocytes) or immunoadsorbtion.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pemphigus Disease
Keywords
Corticothérapy, Rituximab, therapeutic efficacity, therapeutic tolerance
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Rituximab
Arm Type
Experimental
Arm Title
Corticotherapy
Arm Type
Active Comparator
Arm Description
General Corticotherapy
Intervention Type
Drug
Intervention Name(s)
General Corticotherapy
Intervention Description
for patients with severe pemphigus : general corticotherapy Arm : 1.5mg/kg/d for 1 month, then 1.25mg/kg/d for 1 month, then 1mg/kg/d for 1 month, then 0.75 mg/kg/d for 1 month, then 0.5 mg/kg/d for 3 months, then 0.3 mg/kg/d for 3 months, then 0.2 mg/kg/d for 4 months, then 0.1 mg/kg/d for 4 months, for patients with moderated pemphigus : general corticotherapy Arm : 1mg/kg/d for 1 month, then 0.75mg/kg/d for 1 month, then 0.5mg/kg/d for 2 months, then 0.3 mg/kg/d for 2 months, then 0.2 mg/kg/d for 3 months, then 0.1 mg/kg/d for 3 months,
Intervention Type
Drug
Intervention Name(s)
Rituximab
Intervention Description
for patients with severe pemphigus : rituximab Arm : 1mg/kg/d for 1 month, then 0.75 mg/kg/d for 1 month, then 0.5 mg/kg/d for 1 month, then 0.3 mg/kg/d for 1 month, then 0.2 mg/kg/d for 1 month, then 0.1 mg/kg/d for 1 month for patients with moderated pemphigus : rituximab Arm : 0.5mg/kg/d for 1 month, then 0.30 mg/kg/d for 1 month, then 0.2 mg/kg/d for 1 month,
Primary Outcome Measure Information:
Title
Number of patients with pemphigus controlled 24 months after the start of Rituximab treatment
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Number of patients with pemphigus with both cutaneous and mucosal lesions healing after 6 months of rituximab treatment
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age >=18 and <= 80years
consent obtained from patient
effective female contraceptive method for women in procreate age
new case of pemphigus vulgaris (PV) or pemphigus foliaceus (PF)
Exclusion Criteria:
pemphigus vulgaris (PV) or pemphigus foliaceus (PF) treated
pregnant woman or nursing mother
woman able to have a baby and without contraception during the clinical trial period
age < 18 or > 80
karnovsky < 50%
serious antecedents of allergy or anaphylactic reaction with human monoclonal antibody
patient with depletion lymphocytic treatment in the next month
unstable angina or ischemic heart disease
cardiac insufficiency
cardiac rhythm trouble uncontrolled
positive HIV serology
positive hepatitis B and / or C serology
no consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pascal JOLY, Professor
Organizational Affiliation
Clinique Dermatologique - Hôpitaux de Rouen
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Rouen - Hôpitaux de Rouen
City
Rouen
State/Province
Seine Maritime
ZIP/Postal Code
76031
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
32186656
Citation
Mignard C, Maho-Vaillant M, Golinski ML, Balaye P, Prost-Squarcioni C, Houivet E, Calbo SB, Labeille B, Picard-Dahan C, Konstantinou MP, Chaby G, Richard MA, Bouaziz JD, Duvert-Lehembre S, Delaporte E, Bernard P, Caux F, Alexandre M, Ingen-Housz-Oro S, Vabres P, Quereux G, Dupuy A, Debarbieux S, Avenel-Audran M, D'Incan M, Bedane C, Beneton N, Jullien D, Dupin N, Misery L, Machet L, Beylot-Barry M, Dereure O, Sassolas B, Benichou J, Joly P, Hebert V; French Study Group on Autoimmune Bullous Skin Diseases. Factors Associated With Short-term Relapse in Patients With Pemphigus Who Receive Rituximab as First-line Therapy: A Post Hoc Analysis of a Randomized Clinical Trial. JAMA Dermatol. 2020 May 1;156(5):545-552. doi: 10.1001/jamadermatol.2020.0290.
Results Reference
derived
PubMed Identifier
28342637
Citation
Joly P, Maho-Vaillant M, Prost-Squarcioni C, Hebert V, Houivet E, Calbo S, Caillot F, Golinski ML, Labeille B, Picard-Dahan C, Paul C, Richard MA, Bouaziz JD, Duvert-Lehembre S, Bernard P, Caux F, Alexandre M, Ingen-Housz-Oro S, Vabres P, Delaporte E, Quereux G, Dupuy A, Debarbieux S, Avenel-Audran M, D'Incan M, Bedane C, Beneton N, Jullien D, Dupin N, Misery L, Machet L, Beylot-Barry M, Dereure O, Sassolas B, Vermeulin T, Benichou J, Musette P; French study group on autoimmune bullous skin diseases. First-line rituximab combined with short-term prednisone versus prednisone alone for the treatment of pemphigus (Ritux 3): a prospective, multicentre, parallel-group, open-label randomised trial. Lancet. 2017 May 20;389(10083):2031-2040. doi: 10.1016/S0140-6736(17)30070-3. Epub 2017 Mar 22.
Results Reference
derived
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Comparison Between Rituximab Treatment and General Corticotherapy Treatment in Patients With Pemphigus
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