Actively Recruiting
Randomized Clinical Trial Comparing the Safety and Efficacy of Rituximab Versus Oral Cyclophosphamide in Severe Forms of Mucous Membrane Pemphigoid
Led by University Hospital, Rouen · Updated on 2026-02-18
130
Participants Needed
27
Research Sites
398 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Mucous membrane pemphigoid (MMP) describes a group of chronic auto-immune bullous diseases (AIBD) of the basement membrane zone (BMZ), characterized by predominant or exclusive mucosal involvement, including oral, naso-pharyngeal, laryngo-tracheal, genital, oesophageal, anal and ocular mucous membranes. Circulating autoantibodies are directed against various antigens of the BMZ: BP180, laminin 332 and type 7 collagen. MMP is a rare disease with an incidence of 1.8 new cases/million inhabitants/year in France. Scar formation which is secondary to initial inflammation, is a characteristic feature of MMP, leading to major disability (e.g blindness and oesophageal, anal, vaginal stenosis) and life-threatening situations (e.g. laryngeal stenosis leading to respiratory failure). Dapsone is the first line treatment of mild/moderate forms of MMP. Dapsone is used both as initial treatment, and as maintenance therapy. However, severe forms of MMP can rapidly worsen leading to blindness, aphagia due to esophageal stenosis, respiratory failure due to tracheal or laryngeal stenosis, and urinary and sexual dysfunctions due to genital involvement. These patients are usually treated using immunosuppressive drugs. Indeed, corticosteroids (CS) are not recommended in MMP. Cyclophosphamide was considered as the most effective immunosuppressant in severe forms of MMP, before the use of rituximab, an anti-CD20 monoclonal antibody (MAb). Two series from our group have assessed the advantages and disadvantages of IV pulse and oral administration of cyclophosphamide in MMP. Oral administration seems more rapidly effective with 54% of complete remission (CR) after a median time of 24 weeks (16-52 weeks). The results of 41 patients with severe types of MMP (including a French series of 20 patients) treated with rituximab have been published. Rate of CR after one and two cycles were 66% and 90%, respectively. Clinical improvement was rapid, since a decrease in disease activity was observed after 4 weeks of treatment in 64% of patients. Our results and those of the literature suggest that rituximab might be more effective than cyclophosphamide, which has been considered as the gold standard of treatment in severe forms of disease, up to now.
CONDITIONS
Official Title
Randomized Clinical Trial Comparing the Safety and Efficacy of Rituximab Versus Oral Cyclophosphamide in Severe Forms of Mucous Membrane Pemphigoid
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female patients aged 18 to 80 years with newly or previously diagnosed severe mucous membrane pemphigoid
- Clinical signs include blisters or erosions on mucous membranes with or without scarring
- Skin involvement limited to no more than 2 of 4 bullous pemphigoid criteria
- Linear deposits of IgG, IgA, and/or C3 on basement membrane zone by direct immunofluorescence
- Subepithelial blister confirmed by histology when biopsy is possible
- Severe MMP defined by sight-threatening ocular disease, life-threatening airway or esophageal stenosis, involvement of high-risk mucosal sites, multiple mucosal sites, or severe oral involvement
- Disease not controlled despite at least one month of maximum tolerated dapsone treatment, or no prior dapsone treatment in severe cases
- Patient has read and signed informed consent
- Updated vaccinations as recommended
- Women of childbearing potential agree to use adequate contraception or abstinence during treatment and for 12 months after
- Men agree to abstinence or condom use during treatment and for 12 months after
- Agreement to avoid excessive sunlight exposure during study
- Ability to comply with study protocol as judged by investigator
- Affiliated with or beneficiary of social security
You will not qualify if you...
- Age below 18 or above 80 years
- Non-consenting or unable to be followed regularly
- MMP sequelae without active inflammation
- Brunsting Perry pemphigoid or exclusive skin lesions without mucosal involvement
- Karnofsky performance status below 50%
- Unstable angina or advanced ischemic heart disease within last 3 months
- Severe heart failure (NYHA III/IV) or uncontrolled cardiac disease
- Uncontrolled cardiac rhythm disorders
- Severe bronchial obstruction
- History of malignant disease within last 10 years or current progressive cancer except certain skin and cervical cancers
- Anemia (Hb < 10 g/dL), neutropenia, lymphopenia, thrombocytopenia
- Positive hepatitis B or C serology
- Liver or major kidney insufficiency (creatinine clearance ≤ 30 ml/min)
- Active or recent (within 24 weeks) alcohol or drug abuse
- Positive HIV test
- Severe immune deficiency
- Active infections or recent infections requiring oral or IV antibiotics
- History of severe infections within past year
- Uncontrolled concomitant diseases that prevent participation
- Use of oral or systemic corticosteroids within 12 weeks prior to randomization
- Major surgery within 4 weeks before randomization
- Immunosuppressive treatments or other active treatments for MMP within 4 weeks before baseline
- Intravenous immunoglobulins or plasmapheresis within 8 weeks before randomization
- Previous treatment with cyclophosphamide or rituximab
- Previous B cell-targeted therapy other than rituximab
- Live or attenuated vaccine within 28 days before randomization
- Contraindications to study drugs or their excipients
- Lactose intolerance
- Lack of peripheral venous access
- Pregnancy, lactation, or planning pregnancy within study and 12 months after
- Participation in another interventional clinical trial within 28 days prior to randomization
- Judicial or administrative restrictions such as guardianship or deprivation of liberty
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Trial Site Locations
Total: 27 locations
1
CHU Amiens
Amiens, France
Actively Recruiting
2
CHU Angers
Angers, France
Actively Recruiting
3
CH Argenteuil
Argenteuil, France
Actively Recruiting
4
CHU Bordeaux
Bordeaux, France
Actively Recruiting
5
Brest University Hospital
Brest, France
Actively Recruiting
6
CHU Caen
Caen, France
Actively Recruiting
7
CHU Clermont Ferrand
Clermont-Ferrand, France
Actively Recruiting
8
CHU Dijon
Dijon, France
Actively Recruiting
9
CH Le Mans
Le Mans, France
Actively Recruiting
10
CHU Lille
Lille, France
Actively Recruiting
11
CHU de Limoges
Limoges, France
Actively Recruiting
12
HCL
Lyon, France
Actively Recruiting
13
APHM La Timone
Marseille, France
Actively Recruiting
14
CHU Montpellier
Montpellier, France
Actively Recruiting
15
CHU Nantes
Nantes, France
Actively Recruiting
16
CHU Nice
Nice, France
Actively Recruiting
17
APHP Avicennes
Paris, France
Actively Recruiting
18
APHP Bichat
Paris, France
Actively Recruiting
19
APHP Cochin
Paris, France
Actively Recruiting
20
APHP Henri Mondor
Paris, France
Actively Recruiting
21
APHP Pitié Salpétrière
Paris, France
Actively Recruiting
22
APHP Saint-Louis
Paris, France
Actively Recruiting
23
CH Quimper
Quimper, France
Actively Recruiting
24
CHU de Reims
Reims, France
Actively Recruiting
25
CHU Rennes
Rennes, France
Actively Recruiting
26
CHU saint-Etienne
Saint-Etienne, France
Actively Recruiting
27
CHU Tours
Tours, France
Actively Recruiting
Research Team
P
Pascal JOLY, Pr
CONTACT
J
Julien BLOT
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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